Dipeptidyl Peptidase-like Protein 6 (DPP6) is widely expressed in the brain where it co-assembles with Kv4 channels and KChIP auxiliary subunits to regulate the amplitude and functional properties of the somatodendritic A-current, ISA. Here we show that in cerebellar granule (CG) cells DPP6 also regulates resting membrane potential and input resistance by increasing the amplitude of the IK(SO) resting membrane current. Pharmacological analysis shows that DPP6 acts through the control of a channel with properties matching the K2P channel TASK-3. Heterologous expression and co-immunoprecipitation shows that DPP6 co-expression with TASK-3 results in the formation of a protein complex that enhances resting membrane potassium conductance. The co-regulation of resting and voltage-gated channels by DPP6 produces coordinate shifts in resting membrane potential and A-current gating that optimize the sensitivity of ISA inactivation gating to subthreshold fluctuations in resting membrane potential.
Citation: Nadin BM, Pfaffinger PJ (2013) A New TASK for Dipeptidyl Peptidase-like Protein 6. PLoS ONE 8(4): e60831. doi:10.1371/journal.pone.0060831
Editor: Vladimir E. Bondarenko, Georgia State University, United States of America
Received: November 29, 2012; Accepted: March 3, 2013; Published: April 9, 2013
Copyright: © 2013 Nadin, Pfaffinger. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by National Institutes of Health Grants P01 NS37444, R01 GM090029, P30HD024064, and T32GM008507. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The cerebellum plays a critical role in motor learning and cognitive function by adjusting neuronal firing patterns to match desired behavioral outcomes . Cerebellar granule (CG) cells are the most abundant neuron type in the human body and are responsible for forming the parallel fibers of the cerebellum that provide one of the two main excitatory inputs to Purkinje neurons. Factors regulating CG cell firing are critically important for the function of the cerebellum since more than 150,000 different CG cell inputs converge onto a single Purkinje neuron dendrite . Precise regulation of both resting and voltage-gated channels is required for CG cells to process input signals and generate appropriate output firing. However, cellular mechanisms that underlie the coordinate regulation of resting and voltage-gated channels are poorly understood.
Dipeptidyl peptidase-like protein 6 (DPP6) is an inactive protease homolog that is an important regulator of CG cell excitability. DPP6 was identified as an important component of Kv4 based channels following co-purification from cerebellum . Heterologous expression studies have shown that DPP6 acts in coordination with KChIP auxiliary subunits to regulate the expression level and functional properties of Kv4 based ion channels , , . In mouse CG cells, using a lentiviral based RNAi knockdown and rescue strategy, DPP6 was shown to be required to properly form the Kv4 dependent somatodendritic A-type current (ISA) . Interestingly, knocking down DPP6 also dramatically changes the resting membrane properties of CG cells by increasing the resting input resistance. Although “window” currents from A-type channels can contribute to the regulation of resting input resistance , other potential mechanisms exist by which DPP6 expression could affect excitability. In CG cells, IK(SO), a muscarine sensitive resting membrane potassium current plays an important role in regulating excitability . Previous work has suggested that IK(SO) is most likely formed by K2P type channels, and may in fact be an amalgamation of several different K2P channel types , , , .
K2P channels have emerged as a very important class of channels controlling background or “leak” potassium conductance in many cell types . Structurally K2P channels dimerize to form a pore structure that is very similar to other potassium channels due to the presence of two P-loop domains within each subunit , . Previous studies on IK(SO) have indicated the likely importance of the TASK type K2P potassium channels in forming IK(SO) , , , . Similar to IK(SO), TASK-1 and TASK-3 conductances are outwardly rectifying, suppressed by muscarine and likely form functional heteromultimers in many systems , . TASK channels are named due to their high sensitivity to lowered pH (TWIK related Acid Sensitive K+ channel) , and can be differentiated from other muscarine or acid sensitive conductances by their relative sensitivity to other blockers such as extracellular Zn2+ .
The focus of this study was to determine the mechanism by which knockdown of DPP6 results in such dramatic changes in the excitability of CG cells. Here we report that in addition to regulating ISA, DPP6 expression is also required to produce normal levels of IK(SO) in CG cells. Pharmacology and heterologous expression studies show that a regulation of the K2P channel TASK-3 by DPP6 likely underlies this change in IK(SO). We propose that co-regulation of ISA and IK(SO) by DPP6 may be part of an information processing system in the brain that optimally couples ISA channel inactivation to the preceding pattern of subthreshold membrane potential fluctuations.
Materials and Methods
Electrophysiological Methods and Data Analysis
Voltage clamp to isolate ISA and current clamp recordings were performed on cultured CG cells as described previously . For current clamp recordings pipettes were backfilled with internal solution containing (in mM): 120 K-gluconate, 20 KCl, 10 HEPES, 0.2 EGTA, 2 MgCl2, 4 Mg·ATP, 0.3 Tris·GTP, 5 phosphocreatine-2Na+, pH 7.3. Current clamp external solution contained (in mM): 125 NaCl, 2.5 KCl, 25 NaHCO3, 2 CaCl2, 1 MgCl2 10 glucose. Reported potentials are adjusted by −14 mV from the recorded membrane potentials to compensate for electrode junction potential. For pharmacological block experiments, pharmacological agents were dissolved in a modified external solution pH buffered by HEPES containing (in mM): 125 NaCl, 2.5 KCl, 10 HEPES, 2 CaCl2, 1 MgCl2, 10 glucose, pH 7.4. Zn2+ was added to a final concentration of 500 µM, muscarine was added to a final concentration of 10 µM and pH 6 buffer adjusted with HCl, respectively, for each experimental block condition. External blocking solutions were applied using pulled narrow-bore borosilicate glass connected to a PicoSpritzer III (Parker Hannifin Corp., Mayfield Heights, OH) at pressures below 4 psi. Solutions were applied for at least 30 s before initiating recording of the block condition.
Molecular Methods and Primary Cell Culture
Lentiviral vectors used in this study were described previously . As described previously , the Control vector for these studies is identical to the mDPP6 RNAi vector only with a nonspecific RNAi sequence in place of the mDPP6 RNAi target sequence. In our previous work, mDPP6 RNAi was found to be selective for mouse DPP6 and to not affect the expression of human or rat DPP6 . To establish the specificity of mDPP6 RNAi effects, rescue was performed with a mDPP6 RNAi lentiviral vector co-expressing rat DPP6 (rDPP6K, which is normally expressed in CG cells , was used unless specifically indicated otherwise). Heterologous expression studies were performed with mDPP6K. Mouse CG cell cultures were prepared as described previously . All CG cell experiments were conducted at 14–18 days in vitro at which time the neurons show strong repetitive firing. Some Preliminary studies were performed at 8–10 days in vitro , but we found that neurophysiological properties are changing at this age and don’t become stabilized until two weeks in culture. By that time, resting membrane properties and neuronal firing patterns stabilize and become more similar to in vivo, and the conductance changes in response to mDPP6 RNAi are much greater.
Mouse TASK-3 (mKCNK9) was cloned by PCR from a mouse cerebellum cDNA library generated from post-natal day 7 C57/B6J pups using a 5′ UTR primer (5′ TTAGCATCTCCTTCTTCGCGG 3′) and 3′ UTR primer (5′ TGCATGACAAATGATTCTTCC 3′). HA-mKCNK9 was generated by PCR using a 5′ primer incorporating the HA-tag (5′ TTTGAATTCGCCACCATGTA TCCATATGACGTCCCAGACTATGCTATGAAGCGGCAGAAC 3′) and a mKCNK9 internal primer (5′ TCTTCGGCTTTAAGTTTCTCC 3′). HA-DPP6K was generated by PCR using a 5′ primer incorporating the HA-tag (5′ TTTCAATTGGCCACCATGTA TCCATATGACGTCCCAGACTATGCTATGAAGGAAAAGGCA 3′) and a DPP6k internal primer (5′ TTGTTTCAACATTCCGCAGTA 3′).
For analysis of expression of K2P channel variants in CG cell cultures, we used qRT-PCR with Fast SYBR Green Master Mix (Applied Biosystems) on a PTC-200 thermal cycler (MJ Research). Intron spanning primers against K2P channel subunits that are expressed in cerebellum at a similar age were used : TASK-1, forward (5′ AGGAGCTGGAGCGCGTCGTGC 3′), reverse (5′ ACCTTGCCTCCGTCCGTGCTG 3′); TASK-3, forward (5′ AGTCTGAGCCCCACCGCGCTG 3′), reverse (5′ CCAGCATCAGTTCCAGGTGCA 3′); TREK-1 forward (5′ GCCCAGCATGCCTGCGTCAAC 3′), reverse (5′ GGATAATCCCTGCGTTTATTG 3′); TREK-2 forward (5′ CATCTGTGTGAGTCCCCAGGA 3′), reverse (5′ GACTCCCGCGTTATCAGCATC 3′), TWIK-1 forward (5′ TGGAATTGGGACTTCACCTCG 3′), reverse (5′ CCATCTGACAGGGGCACCGTG 3′); TWIK-2 forward (5′ TCGCCAGCACGCTTGTCACCA 3′), reverse (5′ CATCTGTCAGTGGGGTCGTGT 3′). qPCR reactions were verified by melting curves, amplicon agarose gel electrophoresis and amplicon TA cloning and sequencing. All constructs were verified by DNA sequencing.
Heterologous Expression Studies
CHO cells were maintained in DMEM supplemented with 10% fetal bovine serum, penicillin/streptomycin and L-proline. CHO cells were transfected in a 24-well plate format utilizing Lipofectamine 2000 (Invitrogen) and 1 µg total DNA (either GFP 1 µg; mKCNK9 200 ng, GFP 800 ng; mKCNK9 200 ng, DPP6K 300 ng, GFP 500 ng). Voltage-clamp recordings in CHO cells were performed 24 hours post-transfection. HEK cells were cultured as described  and transfected utilizing Lipofectamine 2000.
Immunprecipitation and Western Blotting
24 hours post transfection cells were homogenized in sucrose buffer (in mM, 320 sucrose, 1 EDTA, 5 TRIS, pH 7.4, supplemented with protease inhibitor cocktail (PIC; Sigma). Homogenate was cleared by a 10 minute spin at 500 rcf and membranes isolated by high-speed centrifugation at 25,000 rcf for 40 minutes. Membrane pellet was resuspended and solubilized for 1 hr at 4°C in TNE buffer (in mM: 50 TRIS, 150 NaCl, 1 EDTA, pH 7.4, 1% TritonX-100) plus PIC. Solubilized membrane fraction was cleared with mouse IgG agarose beads (Sigma) for 2 hr at 4°C. Cleared membrane fractions were incubated for 16 hours at 4°C with monoclonal anti-HA agarose conjugate (clone HA-7, Sigma). Bound complexes were washed four times with TNE buffer and eluted by incubating in Laemmli sample buffer (BioRad) containing 100 mM DTT and PIC at 56°C for 5 minutes. Solubilized protein samples were separated by SDS-PAGE gradient gels (Invitrogen). Due to additional salts and non-ionic detergents in the L and F lanes that are no longer present in the beads, the HA sample sometimes runs slightly faster than other samples. Western blots were performed by transferring onto a PVDF membrane and probing with anti-DPP6 antibody (ab41811, 1:1000, Abcam) or anti-KCNK9 antibody (APC-044, 1:500, Alomone labs, Jerusalem, Israel) and detected with HRP conjugated secondaries using PicoSignal ECL (Pierce). TASK-3 protein predominantly runs in our gels at higher molecular weights than predicted for the free monomer, possibly due to aggregation, as has been seen by others . Initial Westerns were performed using film, but later Westerns were exposed digitally using an ImageQuant LAS4000 (GE). Sample loading amounts compared to “L” load are: HA: 2x, Flow thru: 0.25x. Western quantification was performed using ImageQuant software with “rubber band” background subtraction. To determine the efficiency of the co-IP, we measured the fraction of the Load protein that was immunoprecipitated depending upon whether the protein was tagged or not. The ratio of the fraction immunoprecipitated indirectly when untagged divided by the fraction directly immunoprecipitated when tagged is the Co-IP ratio. This ratio corrects for systematic inefficiency in the immunoprecipitation and detection protocol.
Data Analysis and Statistics
Data analysis was performed using Clampfit10 (Molecular Devices), OriginPro7 (OriginLab), and Excel (Microsoft). Statistical analyses were performed using OriginPro7 and Analyse-it for Excel (Analyse-it) and on-line servers (http://www.graphpad.com/quickcalcs/index.cfm; http://elegans.som.vcu.edu/~leon/stats/utest.html). Data sets were not significantly different from normality using the Shapiro-Wilks test. P values were determined using both independent two-tailed t-test and the non-parametric Mann Whitney U test, both of which gave the same results for significance testing at our alpha level of P = 0.05. Reported P values are from t-test. I–V curves were compared using ANOVA on the multiple regressions with OriginPro7. All comparisons reported were significantly different unless otherwise indicated by NSD (Not Significantly Different). I–V curves were compared by one-way ANOVA on the voltage step series. Modeling of DPP6 sensitive current pharmacology was done with the function: y = Ps(x−Ns)/x, where x is the resting conductance, y is the fraction of the resting conductance that is blocked by the treatment, NS-Total mDPP6 RNAi insensitive rest conductance, and PS is the sensitivity of TASK-3 channels to the treatment. NS was fixed at 1.1 nS based on the average Grest for mDPP6 RNAi treated neurons. PS was determined by non-linear least squares fit to the data and is indicated by the dashed line. Membrane corner frequency (fc) was calculated as fc = 1/(2πτm). Power spectra and RMS values were calculated by subtracting the average signal from the record to obtain fluctuations around zero. Power Spectra were calculated by FFT using OriginPro. RMS was calculated by taking the square root of the average for the square of the fluctuations around 0. Inactivation sensitivity was calculated by dividing the channel Inactivation standard deviation (in %) by the standard deviation for the membrane potential fluctuations.
CG cell modeling was performed using a single 12.5 µm diameter compartment NEURON model , . A stochastic synaptic current noise generator previously developed by Destexhe et al, 2001  was added to examine the effects of synaptic noise on channel gating. Excitatory and inhibitory fluctuations were varied by specifying the average conductance (Ge, Gi), standard deviation (SDe, SDi). Time constants (τe = 2.728 ms, τi = 10.49 ms) and zero current potential (Ee = 0 mV, Ei = −85 mV) were not varied. Both Control and mDPP6 RNAi CG cell models used the Na+ channel (GNa = 0.1 S/cm2), Ca2+ channel (GCa = 0.6 µS/cm2), Kv channel (GK = 0.18 mS/cm2) and KCa2+ (GKCa = 1.5 mS/cm2) channel models previously developed for CG cells , .To better describe the multiple exponential components found in the gating of the native ISA channel we switched from H&H type models to multi-state models developed using QuB . The Kinetic model for ISA following mDPP6 RNAi treatment (GISA(R)) only allows for inactivation through closed states. The Control condition ISA model (GISA(C)) has accelerated kinetics and adds additional states for N-type inactivation produced by DPP6a  and a deeper closed inactivation state produced by DPP6K . Fits of these models to the steady state and kinetic properties of native channels ISA is shown in Figure S1. TASK-3 (GTASK-3) was modeled with two independent gates as described previously . The mDPP6 RNAi resistant K2P current (GK2P) was identical except one gate was made slightly faster and more voltage dependent to better fit the resting current following mDPP6 RNAi treatment. A small Na+ selective linear leak component (GL) was added to account for a resting potential more positive than EK. The Control CG model added GISA(C), GTASK-3, GK2P, and GL. The mDPP6 RNAi CG model added GISA(R), GK2P, and GL. Reversal potentials were set at: ENa = 60 mV, EK = −91.5 mV.
The procedures on animals conducted in this work were performed in strict accordance with Animal Welfare Act, the Public Health Services Animal Welfare Policy, and The National Institute of Health Guide for Care and Use of Laboratory Animals. The experimental protocol was approved by the Institutional Animal Care and Use Committees (IACUC) of Baylor College of Medicine (Protocol Number: AN-752). Following the approved protocol, every effort was made to minimize suffering.
DPP6 Regulates the Excitability of Cerebellar Granule Neurons Independent of Kv4.2 Channels
Application of a lentiviral vector expressing RNAi targeting a mouse DPP6 (mDPP6) core sequence dramatically increases the excitability of mouse CG cells. In Fig. 1A we show a representative CG cell current clamp recording where the neurons have been infected with a lentiviral vector expressing only EGFP (Wild Type). On average such wild type recordings require 125±10 pA of current injection to reach threshold. In contrast, if the same neurons are infected with a lentiviral vector also expressing mDPP6 RNAi (+mDPP6 RNAi), the neurons begin to fire in response to much smaller current injections (+mDPP6 RNAi: 22±6 pA (P<0.0001)). To determine if these effects are mediated through changes in ISA “window” currents  or are an unexpected consequence of manipulating DPP6 protein levels, we sought to disrupt ISA while still preserving DPP6. Knockout of the KCND2 gene (Kv4.2 KO) eliminates Kv4.2 protein and reduces ISA in CG cells by approximately 80%, similar to mDPP6 RNAi . Interestingly, DPP6 protein levels remain high in Kv4.2 KO neurons, although KChIPs, another class of ISA auxiliary subunit protein, are almost completely lost when Kv4.2 is knocked out , , , , . The Kv4.2 KO mice therefore provides an interesting way to potentially distinguish between DPP6 effects mediated through ISA and those that are not.
Figure 1. DPP6 regulates excitability of CG cells independent of its control of Kv4 channels.
Mouse CG cells were recorded by current clamp following infection with a lentiviral vector expressing EGFP (control) or EGFP plus mouse DPP6 RNAi (+mDPP6 RNAi). A) Sustained current injections, duration indicated by black bar, were given at the level indicated to the right of the trace (pA) to elicit action potential firing (Red bar indicates 1 s). Following treatment with mDPP6 RNAi, threshold current is reduced and cells fire in response to much smaller current injections. B) Threshold current in CG cells from Kv4.2 KO animals is similar to wild type despite the large reduction in ISA amplitude. Threshold current in CG cells from Kv4.2 KO animals remains sensitive to mDPP6 RNAi showing that the regulation of threshold by DPP6 is independent of the level of ISA. C) Current required for initiation of action potentials under different conditions is plotted as a cumulative distribution plot. Holding current indicated by the triangles was applied to set a common resting potential of −85 mV. In CG cells from both Wild Type (n = 14) and Kv4.2 KO (n = 10) animals, treatment with mDPP6 RNAi (WT, n = 13; Kv4.2 KO, n = 11) significantly reduces the current required for action potential initiation (WT,Kv4.2 KO: P<0.0001) by around 100 pA.doi:10.1371/journal.pone.0060831.g001
As the representative recording in Fig. 1B shows, CG cells from Kv4.2 KO animals (Kv4.2 KO) have a firing threshold similar to that of wild type CG cells (Kv4.2 KO: 156±12 pA, NSD, P = 0.055). We next tested whether threshold current in these Kv4.2 KO CG cell remain sensitive to mDPP6 RNAi. The representative recordings from a Kv4.2 KO CG cell treated with mDPP6 RNAi (+mDPP6 RNAi, Fig. 1B) shows that despite the large reduction of ISA in the cells threshold current drops dramatically (+mDPP6 RNAi: 49±10 pA (P<0.0001)). Cumulative distribution functions for the current required to reach threshold were computed for the different conditions (Fig. 1C). Although there is consistently a slightly higher threshold current (~20 pA) for Kv4.2 KO compared to wild type treated under similar conditions (possibly reflecting some compensatory changes in the knockout ), mDPP6 RNAi treatment reduces threshold current by about 100 pA in CG cells from both wild type and Kv4.2 KO animals (WT: 96±13.6 pA, Kv4.2 KO: 108±15.3 pA, NSD (P = 0.58)). We therefore conclude that the effect of DPP6 on threshold current is independent of the level of ISA and likely involves an alternate regulatory pathway.
DPP6 Controls Excitability by Modulating the Level of IK(SO) in CG Cells
Biophysical analysis of CG cells treated with mDPP6 RNAi reveals a significant positive shift in resting membrane potential (P<0.0001) (Fig. 2A) and a significant increase in input resistance (P<0.0001) (Fig. 2B). Because membrane capacitance remains stable, this suggests that DPP6 increases the level of a resting membrane conductance. To confirm that these RNAi effects are due to the specific loss of DPP6, we performed rescue experiments by adding a rat DPP6 (rDPP6) expression cassette to our mDPP6 RNAi expressing lentiviral vectors. Our previous studies showed that rDPP6 is resistant to mDPP6 RNAi due to alternative codon usage in the RNAi target sequence . We tested for rescue with two rDPP6 N-terminal variants, rDPP6a and rDPP6K, which are co-expressed at high levels in CG cells , , . Both variants were able to rescue resting membrane potential and input resistance (compared to mDPP6 RNAi: ERest, rDPP6a (P = 0.01), rDPP6K (P<0.0001); Input Resistance, rDPP6a (P<0.0001), rDPP6K (P<0.0001)), although rDPP6K rescue was generally significantly more robust (compared to rDPP6a: ERest (P = 0.008), Input Resistance (P = 0.0009)) and was used for all subsequent rescue experiments unless otherwise stated (Fig. 2A, B). As predicted by our previous results, CG cells from Kv4.2 KO animals are similar to wild type in resting membrane potential and input resistance, and both properties remain equally sensitive to mDPP6 RNAi treatment and rescue (Fig. 2A, B). Based on these observed effects we hypothesized that the excitability changes produced by DPP6 knockdown could be due to the specific loss of a resting membrane potassium conductance which would normally drive the resting membrane potential to more negative values.
Figure 2. DPP6 regulates an outwardly rectifying resting membrane potassium conductance.
CG cells were treated with lentiviral vectors expressing EGFP (control: WT (n = 32); Kv4.2 KO (n = 9)) or mDPP6 RNAi (WT (n = 13), Kv4.2 KO (n = 6)) to knockdown DPP6. For rescue experiments the lentiviral vectors also co-expressed rat DPP6 (rDPP6), which is insensitive to the mouse DPP6 RNAi due to coding differences in the RNAi target sequence. Both rDPP6K and rDPP6a splice variants, which are highly expressed in CG cells, were tested (rDPP6K: WT (n = 32); rDPP6a: WT (n = 31), Kv4.2 KO (n = 4)). A) Knockdown of mDPP6 causes a depolarization of the resting membrane potential which is reversed by co-expression of rDPP6. Results for wild type and Kv4.2 KO animals are indistinguishable (NSD: control (P = 0.33); mDPP6 RNAi (P = 0.72); rDPP6a (P = 0.85)). (data plotted ± SEM). B) Resting input resistance is increased for CG cells following RNAi treatment and this effect is reversed by co-expression of rDPP6. Results between CG cells from control and Kv4.2 KO animals are indistinguishable (NSD: control (P = 0.15); mDPP6 RNAi (P = 0.74); rDPP6a (P = 0.72)). (data plotted ± SEM). C) Average membrane current versus membrane potential for control (n = 24) and mDPP6 RNAi (n = 13) treated CG cells. Knockdown of DPP6 reduces the amplitude of an outwardly rectifying current (P = 0.0002). Smooth curves were generated with NEURON using the following conductances (mDPP6 RNAi: GK2P = 60 nS; GL = 0.133 nS; Control: Same+GTASK-3 = 30 nS). Inset expands the axes near the resting membrane potential to show that a linear Ohmic fit to this current can explain the change in input resistance (Slope change) and Erest (0 current potential shift). (data plotted ± SEM). D) Difference current for mDPP6 RNAi treated cells compared to control shows that the RNAi sensitive current is outwardly rectifying and reverses near −90 mV as expected for a potassium selective conductance. (data plotted ± SEM). Smooth curve shows TASK-3 model fit to the data (GTASK-3 = 30 nS). e) Representative voltage clamp traces show that the conductance regulated by mDPP6 RNAi is outwardly rectifying similar to IK(SO) conductance previously described in CG cells. Scale bar: 200 pA, 100 ms.doi:10.1371/journal.pone.0060831.g002
To better characterize the DPP6 dependent conductance, a series of experiments was performed to compare the sustained membrane current versus voltage relationship between control and mDPP6 RNAi treated CG cells. As shown in Fig. 2C, the sustained membrane current of CG cells is outwardly rectifying and loss of DPP6 reduces the size of this current (P = 0.008). The inset of Fig. 2C expands the membrane potential axis around the resting potential to better show that this change in the sustained current voltage relationship underlies the observed changes in membrane zero current potential (ERest) and resting input resistance. A DPP6 dependent current was constructed by taking the difference between the average membrane current with and without DPP6 RNAi treatment (Fig. 2D). This analysis shows that the general shape of the I-V curve for the DPP6 dependent current is also outwardly rectifying, with a reversal near EK. Representative voltage clamp recordings from wild type control and mDPP6 RNAi treated CG cells show that the membrane conductance being regulated by DPP6 is rapidly outwardly rectifying, similar to the previously described IK(SO) of CG cells (Fig. 2E) , .
Pharmacology of DPP6 Dependent Current Matches TASK-3
In CG cells, previous studies have shown that K2P channels play an important role in regulating resting membrane potential and input resistance and likely underlie IK(SO) , , , . To determine if a channel in this gene family is responsible for forming the DPP6 dependent current, qRT-PCR was performed on our CG cell cultures to measure the relative expression levels of different K2P channels (Fig. 3A). qRT-PCR identifies TASK-3 as the most highly expressed K2P subunit found in these neurons (P<0.0001). Since TASK-3 forms a rapidly outwardly rectifying potassium conductance, we hypothesized that TASK-3 was a likely candidate underlying the DPP6 dependent current , , and therefore tested if the conductance being regulated by DPP6 has pharmacology similar to that of TASK-3 channels. TASK channels are named for their sensitivity to block by external acidification, and we can pharmacologically distinguish between the related TASK-3 and TASK-1 proteins because only TASK-3 is highly sensitive to block by external Zn2+ , , , . Fig. 3B shows representative voltage response of CG cells to a series of 10 pA current injections given before and after application of external pH 6.0 to examine the potential role of TASK channels in establishing the CG cells resting membrane conductance properties. In control cells, as expected for a significant TASK conductance, application of external pH 6.0 results in a large increase in amplitude of the elicited voltage deflections due to the block of a portion of the resting membrane conductance. However, in mDPP6 RNAi treated CG cells there is almost no effect of external pH 6.0 application. The loss of an acid sensitive conductance can be completely reversed by co-expression of RNAi resistant rDPP6, demonstrating that this effect is specifically due to the loss of DPP6. To directly compare the sensitivity of the DPP6 regulated conductance to TASK-3, we over expressed TASK-3 in CG cells and measured its pharmacological sensitivity. As expected, TASK-3 expression produces a dramatic increase in resting conductance that is sensitive to block by external pH 6.0.
Figure 3. DPP6 regulates a channel with properties similar to TASK-3.
A) SYBR-Green qRT-PCR on cDNA made from mRNA isolated from our CG cell cultures. Following primer optimization, expression levels were determined by the Ct0.1 values (n = 6 for each). Five different K2P channels could be detected with TASK-3 abundance about equal to the other four combined. TWIK-2 could not be detected (N.D.). (data plotted ± SEM). B) Sensitivity of membrane conductance to treatment with pH 6.0 external solution. Current clamp recordings from cells before and after application of pH 6.0 external solution show changes in the voltage responses to a series of 10 pA current steps. For these studies we only characterized changes in input conductance because pH 6.0 partially blocks voltage gated channels Na+ channels, making an analysis of effects of low pH on firing threshold complex and essentially uninformative for our purposes . Control cells show much larger voltage responses following low pH application indicating that a significant fraction of the resting membrane conductance is pH sensitive. Treatment with mDPP6 RNAi decreases resting membrane conductance to levels similar to control CG cells treated with low pH while also eliminating sensitivity to low pH. Co-expression of rDPP6 restores sensitivity to low pH. TASK-3 driven by a CMV promoter was expressed in CG cells using a lentiviral vector to determine the sensitivity of TASK-3 to low pH in this expression system. As expected expression of high levels of TASK-3 dramatically increases membrane resting conductance, much of which is sensitive to block by external pH 6.0. Scale bar: 20 mV, 50 ms. C) Summary results testing sensitivity of the resting conductance to external pH 6.0 (WT (n = 11), mDPP6 RNAi (n = 5), rDPP6 Rescue (n = 8), TASK-3 (n = 6)), 500 µM external Zn2+ (WT (n = 6), mDPP6 RNAi (n = 5), rDPP6 Rescue (n = 6), TASK-3 (n = 6)) and suppression by 10 µM muscarine (WT (n = 8), mDPP6 RNAi (n = 5), rDPP6 Rescue (n = 4), TASK-3 (n = 6)). Results show that treatment with mDPP6 RNAi eliminates sensitivity to these blockers which is rescued by co-expression of rDPP6. Over expression of TASK-3 produced the highest sensitivity. Data points were well fit (solid line) assuming a single TASK-3 sensitivity (dashed line) for conductance levels above the 1.1 nS of average mDPP6 RNAi insensitive resting conductance in these experiments. (data plotted ± SEM).doi:10.1371/journal.pone.0060831.g003
Fig. 3C summarizes our results for block of the CG cell resting membrane conductance by external pH 6.0, 500 µM external Zn2+, and 10 µM muscarine following infection with various lentiviral constructs. For wild type CG cell, a significant fraction of the resting membrane conductance is sensitive to low pH, Zn2+ and Muscarine suggesting that TASK channels, and TASK-3 in particular, contribute significantly to the resting membrane properties of these cells. Following treatment with mDPP6 RNAi, the sensitivity of the resting membrane conductance to pH 6.0, external Zn2+, and muscarine is almost completely eliminated (Not significantly different from 0(P>0.5)), suggesting that the TASK component of the resting membrane conductance has been lost. The effects of mDPP6 RNAi and can be rescued back to wild type levels by co-expression of RNAi insensitive rDPP6 (compared to mDPP6 RNAi for each condition, P<0.0001). To determine the expected sensitivity of TASK-3 channels in our CG cells to these treatments, we over expressed TASK-3 using a lentiviral vector. As expected the pH, Zn2+ and muscarine sensitive components of the resting membrane conductance greatly increase as the levels of TASK-3 conductance increases. We used a simple model to fit these data where the resting membrane conductance of CG cells is assumed to be composed of two populations of channels, a DPP6 dependent TASK-3 channel and a DPP6 insensitive non-TASK K2P channel. Using this model with two free parameters, the amplitude of non-TASK K2P conductance (x-intercept), and the sensitivity of TASK-3 to the treatment (y-axis asymptote, dashed lines) we could explain the observed results (solid lines) (muscarine: r2 = 0.75; pH 6.0: r2 = 0.98, Zn2+: r2 = 0.87). Although DPP6 regulation of TASK-3 is sufficient to explain our results, we cannot rule out the importance of TASK-1/TASK-3 heteromultimers or the co-regulation of other K2P channels that might require TASK-3 for functional expression or the potential regulation by DPP6 of other K2P channels not expressed at high levels in CG cells.
DPP6 Regulates TASK-3 in Heterologous Cells
To determine if DPP6 can specifically regulate TASK-3, we performed heterologous co-expression studies in CHO-K1 cells. CHO-K1 cells have a low resting membrane conductance and a depolarized resting membrane potential (Fig. 4A–C). Expression of TASK-3 produces a rapid outwardly rectifying potassium current (Fig. 4A, B), that hyperpolarizes the resting membrane potential of CHO-K1 cells and increases the resting membrane conductance (Fig. 4C). Co-expression of DPP6 with TASK-3 produces a dramatic increase in the magnitude of the rapid outwardly rectifying potassium current formed by TASK-3 alone (Fig. 4A, B). The addition of DPP6 further hyperpolarizes the resting membrane potential and leads to an additional 2.3 fold increase in the resting membrane conductance (Fig. 4C). To test for co-assembly of DPP6 and TASK-3 into a protein complex, co-immunoprecipitation experiments were performed. When DPP6 and TASK-3 are co-expressed with one protein epitope tagged with HA, they co-precipitate with about a third of the total protein co-precipitating on average, compared to a 4% background signal when neither protein is HA tagged (Fig. 4D). We conclude therefore that DPP6 can bind to a protein complex containing TASK-3 to regulate the level of functional current.
Figure 4. Regulation of TASK-3 by DPP6 in a Heterologous Expression System.
CHO-K1 cells were transfected with GFP alone (GFP (n = 14)), or the addition of TASK-3 (+TASK-3 (n = 16)) or the further addition of DPP6 with TASK-3 (+DPP6 (n = 23)). A) Representative current traces for step depolarizations. Only small currents are observed in CHO cells that are not transfected with channel subunits. Following expression of TASK-3 there is a large outwardly rectifying current expressed that increases further with co-expression of DPP6. Scale bar: 2000 pA, 500 ms. B) Representative current-voltage plots for voltage ramps showing the outward rectifying potassium current produced by TASK-3 is greatly increased by addition of DPP6. Dashed lines are from a NEURON model incorporating a non-selective cationic Leak Channel (EL = −16 mV) and a potassium selective TASK-3 Channel (EK = −91.5 mV). Maximum conductance parameters used to generate these curves (EGFP: GL = 2.81 nS, GTASK-3 = 0 nS; +TASK-3: GL = 1.75 nS, GTASK-3 = 320 nS; +DPP6: GL = 4.25 nS, GTASK-3 = 840 nS). C) Analysis of average changes in resting potential and resting membrane conductance. Membrane property changes produced by TASK-3 (*compared to GFP: ERest(P<0.0001); GRest(P<0.0036)) are further increased by co-expression of DPP6 (# compared to +TASK-3: ERest (P<0.023); GRest (P<0.0001)). (data plotted ± SEM). D) Co-immunoprecipitation was performed to test for direct interactions between DPP6 and TASK-3 followed by Western blots for either DPP6 or TASK-3. Expression conditions indicated at the top of each section. L-Load, HA-precipitated with anti-HA antibody, F-flow through. Red HA indicates a lane where the non-HA tagged protein has been co-immunoprecipitated with the HA-tagged protein. Summary data from 6 co-immunoprecipitation experiments shows that a co-precipitation protocol pulls down about 31.4±4.8% (P = 0.0013) of the protein that could be directly precipitated compared to a background signal of 4.0±1.3% when neither proteins is HA tagged (BKG).doi:10.1371/journal.pone.0060831.g004
Computational Modeling Shows DPP6 Co-Regulation of ISA and IK(SO) Tunes Neuronal Subthreshold Information Processing
To examine the importance of co-regulation of both TASK-3 and ISA channels by DPP6 in shaping CG cell firing and information processing, we constructed channel gating models using QuB for TASK-3(GTASK-3), mDPP6 RNAi insensitive K2P (GK2P), control ISA (GISA(c)) and mDPP6 RNAi residual ISA (GISA(r)) and incorporated these channels as point processes into a single compartment (12.5 µm diameter) NEURON  CG cell model  (Fig. 5). Due to the electrotonically compact somatodendritic compartment in CG cells a multicompartment dendritic model is not necessary; however, accurately capturing some aspects of CG cell firing may require separate axonal and initial segment compartments that we did not try to model in this study , . As described in the Methods, the GISA(c) and GISA(r) models were optimized to fit our recorded CG cell currents (Fig. S1). For GTASK-3 we used a model based on detailed single channel recordings of TASK-3 channels , and slightly modified it to match the conductance properties of the resting K2P conductance, GK2P, found in mDPP6 RNAi treated CG cells (Fig. 5). The GTASK-3 and GK2P models produce a good fit to our data from CG cells (Fig. 2C,D) and to TASK-3 currents expressed in CHO cells with or without DPP6 (Fig. 4B). By switching channel types present under different conditions (Control: GTASK-3, GK2P, GISA(c); mDPP6 RNAi: GK2P, GISA(r)) the CG cell model accurately reproduces the resting membrane potential (Control ERest = −83.5 mV, mDPP6 RNAi ERest = −69.4 mV) and input resistance (Control RIN = 0.49 GΩ, mDPP6 RNAi RIN = 1.06 GΩ) for Control and mDPP6 RNAi treated CG cells. By doubling resting membrane conductance, DPP6 cuts the membrane time constant in half, increasing the frequency response properties of the CG cell membrane particularly in the gamma frequency range (fc: Control = 75 Hz, mDPP6 RNAi = 32 Hz).
Figure 5. Conductance gating models for the different current components used in our CG cell NEURON model.
Rate constants are k(0 mV) rate times the voltage dependence (ea) which is raised to the EM power (mV) to obtain the final rate. Gmax and 0 current potentials are given for each conductance. For ISA models, GISA(c) and GISA(r), the I1−I2 transition between closed inactivated states is generally not rate limiting, and thus effectively invisible, but was adjusted to preserve detailed balances. More complex models have been proposed for ISA, but these models capture the basic gating properties of the ISA channel over a wide range of voltages. For the TASK-3 channel, and the residual K2P current in CG cells remaining after mDPP6 RNAi treatment, GK2P, the model has 2 independent gates which must both be open to conduct. The linear leak component is always open and modeled to be Na+ selective to match the relatively high input resistance of CG cells while still producing the large change in Erest between Control and mDPP6 RNAi CG cells.doi:10.1371/journal.pone.0060831.g005
We next examined the relative importance of ISA and TASK-3 regulation for the changes in excitability produced by mDPP6 RNAi. When the firing of the Control CG cell model in response to current steps of varying amplitude (Fig. 6A1) is compared to the firing of the mDPP6 RNAi CG cell model (Fig. 6A4) the shift in threshold current is very similar to what we see in our recordings (Model: 93 pA; Recordings: 96±13.6 pA). To determine the relative importance of ISA and TASK-3 modulation for producing these changes in firing, we selectively reproduced only the change in ISA produced by mDPP6 RNAi (CG(ISA(R)): GTASK-3, GK2P, GISA(r)) (Fig. 6A2) or only the loss of TASK-3 produced by mDPP6 RNAi (CG(ΔTASK-3): GK2P, GISA(c)) (Fig. 6A4). Fig. 6A2 shows that in the CG(ΔTASK-3) model, the selective loss of TASK-3 reduces threshold current by 80 pA, suggesting that most of the increase in excitability produced by mDPP6 RNAi is due to the loss of this channel. The larger amplitude and more rapid kinetics of the Control ISA is evident by the strong suppression of firing early in the depolarization. In contrast, the CG(ISA(R)) model (Fig. 6A3) shows only a 12 pA decrease in threshold current, but much less suppression of firing early in the depolarization compared to Control.
Figure 6. Co-regulation of Kv4 and TASK-3 channels by DPP6 optimizes the sensitivity of ISA to membrane potential fluctuations.
A) Firing properties of NEURON CG cell models. A1- Control, A2- CG(ΔTASK-3), A3- CG(ISA(R)), a4- mDPP6 RNAi. Current injection magnitude indicated to the right of the trace (pA). Black bar- injection duration, red inset- 1 s. A low level of random noise was added to these simulations (Ge = Gi = 10 pS; SDe = SDi = 50 pS). B) Effect of stochastic synaptic conductance fluctuations on ISA inactivation (Ge = Gi = 25 pS; SDe = SDi = 200 pS). In Control CG model, membrane potential fluctuates around −81 mV. Control ISA (GISA(c)) responds with fluctuations in inactivation near the 0.5 level. For mDPP6 RNAi ISA (GISA(r)) inactivation would be much less (~0.2). In the mDPP6 RNAi CG cell, the mDPP6 RNAi ISA channel inactivation (GISA(r)) is near the 0.5 level, whereas a control ISA channel (GISA(c)) would be around (0.8). GISA(c) inactivation show higher frequency components than GISA(r). C) Power spectra for membrane potential fluctuations in Control and mDPP6 RNAi membranes calculated by FFT using OriginPro. Calculated corner frequencies for Control and mDPP6 RNAi membranes are indicated by triangles. mDPP6 RNAi signals fall off before Control due to a difference in membrane time constant. D) Cross-correlation analysis for ISA inactivation compared to membrane potential fluctuations. Control ISA shows a peak correlation of around 0.55 at 6.4 ms delay to the Control membrane potential fluctuations. For mDPP6 RNAi ISA, the peak correlation is 0.27 at a 15 ms delay to the mDPP6 RNAi cell membrane potential fluctuations. E) Frequency response properties for ISA channel inactivation. 5 mV sinusoidal waves from 0.25–200 Hz centered at −80 mV were fed into the GISA(c) and GISA(r) QuB channel models and the inactivation signal was measured and fit with a sine wave. The RMS amplitude of the fitted sine wave was compared to the inactivation produced by the RMS equivalent DC potential change of ±3.54 mV. The signal fall off at higher frequencies was fit with a double Lorentzian (corner frequencies indicated by drop lines). There is about a 7× shift to higher frequency responses when DPP6 is present in the ISA channel.doi:10.1371/journal.pone.0060831.g006
In addition to direct effects on excitability, co-regulation of Kv4 and TASK-3 channels by DPP6 has important implications for how CG cells processes subthreshold membrane potential fluctuations. ISA channel inactivation changes dramatically in the subthreshold range of membrane potentials, and is thought to be an important short term associative learning signal , , , , . DPP6 greatly accelerates ISA activation and inactivation kinetics , complementing its effects on membrane frequency response. We therefore sought to use our models to examine how mDPP6 RNAi treatment might affect the translation of subthreshold membrane potential fluctuations into different levels of ISA channel inactivation. For these studies we used a stochastic signal generator to introduce excitatory and inhibitory conductance fluctuations to alter membrane potential around rest  (Figure 6B). The amplitudes of current fluctuations were adjusted to produce an average RMS fluctuation of around 2.8 mV in the resting membrane potential for Control (Ge = Gi = 25 pS; SDe = SDi = 200 pS) and mDPP6 RNAi conditions (Ge = Gi = 25 pS; SDe = SDi = 110 pS). Due to the lower membrane corner frequency (fc) in mDPP6 RNAi CG cells, there is less power in these fluctuations at higher frequencies compared to Control (Fig. 6C). For Control and mDPP6 RNAi CG cell models, recorded membrane potential fluctuations were used as input to ISA channel models in QuB to determine the impact on inactivation (Figure 6B). On average, due to coordinate shifts in CG cell resting membrane potential and ISA gating produced by DPP6, ISA steady state inactivation is positioned near the midpoint at rest under both conditions, at the steepest point of the inactivation curve. In contrast, for GISA(c) responses to the mDPP6 RNAi membrane, or GISA(r) responses to the Control membrane, the resting inactivation level of the channel are at one extreme end or the other of the inactivation curve. Although the average values for inactivation are similar for ISA in Control or mDPP6 RNAi treated CG cells, the sensitivity of inactivation to the EM fluctuations is much greater under Control conditions as can be seen by comparing the standard deviation of the resultant inactivation fluctuations to the standard deviation of the input EM fluctuations (SD ratios: Control: 0.9%/mV; mDPP6 RNAi: 0.57%/mV).
To quantify how reliably ISA channels convert membrane potential fluctuations into changes in inactivation, we measured the cross-correlation between inactivation and membrane potential (Fig. 6D). For Control conditions, the peak correlation of ISA channel inactivation with membrane potential is 0.55 at a delay of 6.3 ms. This correlation is not seen in the forward direction and falls off rapidly with a time constant of 35 ms. In contrast, the peak correlation of mDPP6 RNAi ISA channel inactivation with membrane potential is much lower (0.27), peaks later (15 ms), and falls off more slowly with a time constant of 300 ms. We also examined a range of stochastic input parameters (Ge,Gi: 0–50 pS; SDe,SDi: 10–500 pS) and membrane potential offsets, and find similar results. The shape of the cross-correlation plot for the Control condition is strikingly similar to the time course for spike timing dependent plasticity, suggesting that DPP6 expression is likely important in regulating this plasticity signal . To directly compare the frequency responses of the Control and mDPP6 RNAi ISA channels we introduced 5 mV sinusoidal membrane potential fluctuations from 0.25–200 Hz around −80 mV into our QuB ISA models and measured how efficiently these fluctuations were converted into changes in inactivation (Fig. 6E). Models incorporating control ISA channels respond to much higher frequency components, suggesting that the higher frequencies membrane potential fluctuations allowed by DPP6 regulation of TASK-3 channels can only be effectively utilized by ISA channels incorporating DPP6. Taking all these effects together suggests that DPP6 co-regulation serves to facilitate the efficient translation of dynamic fluctuations in membrane potential into significant changes in the level of available ISA.
The idea of ion channel proteins as isolated functional entities has long since been overturned. It is now clear that most channel proteins are complex multipeptide machines that interact with a variety of other cellular components to properly localize, functionally shape, and regulate the ion currents they pass. Recently some integral proteins of ion channel complexes have been shown to have multiple distinct functional roles in a cell. For example, calmodulin plays an integral role in many channels and enzymes, Na+ channel auxiliary subunits have also been identified as important components of voltage-gated potassium channels, KChIPs have been shown to regulate the function of both voltage-gated calcium channels and potassium channels as well as regulate gene transcription, and KCNE1-5 can regulate both KCNQ channels as well as HERG channels and likely other potassium channels , , , , , . While it is easy to envision why the efficient Ca2+ sensing of calmodulin has been co-opted to regulate a number of different protein complexes, including ion channels, it is less clear why so many ion channel auxiliary subunit protein appear to have multiple functional roles.
Prior to these studies the only known role for DPP6 was to regulate Kv4 channel expression and functional properties, and we hypothesized that this regulation was critical to form the native somatodendritic A-type current (ISA) in neurons , , , , , , , . In this study, we add DPP6 to this growing list of multifunctional channel auxiliary subunit proteins by showing it can also co-regulate a resting conductance with functional properties that are similar to TASK-3 channels. Our computational modeling studies suggest a potential new functional role for DPP6 by considering all the physiological changes regulated by DPP6 as part of a whole. In this view, it is clear that DPP6 can be seen to play an important role in speeding up CG cell electrophysiological properties by accelerating channel gating kinetics and increasing the cellular membrane potential frequency response. This suggests an innovative hypothesis, namely that DPP6 has evolved to produce a coordinate regulation of multiple ion channels to produce a dramatic overall change in neuronal functional phenotype. Interestingly, KChIP regulation of voltage-gated Ca2+ channels and Kv4 channels has a related integrative functional role in shaping the excitability of stellate cells , . It therefore seems likely that many auxiliary subunits may be playing similar integrative functional roles by interacting with multiple channel types to shape the excitability properties of neurons and other excitable cells.
While computational modeling clearly suggests an integrative function for DPP6 in shaping CG cell processing of synaptic inputs and firing properties, more work needs to be done to fully establish such a role in vivo. In addition to potential differences in gene expression and protein targeting in vivo, other regulatory factors such as GABA inhibition have not yet been incorporated into our model . Indeed, precise in vivo patterns of mossy fiber release onto CG cells have not been modeled in our studies, and therefore we can only generally describe how DPP6 shapes the frequency response properties of CG cells without being able to better describe when such frequencies are important for cerebellar function. In addition, there are aspects of compartmentalized neuronal function that we have not attempted to capture in our CG cell model. CG cells do not have the large complex dendritic trees of CA1 and cortical pyramidal neurons, although DPP6 does regulate potassium channels in such dendrites and therefore DPP6 co-regulation may play an important role in shaping dendritic tree function in other neurons . Finally, there are important inter-compartment interactions in CG cells between the somatodendritic and axon and axon hillock regions that we have not modeled and may play an important role in regulating CG cell firing in vivo . For the most part, however, incorporating such additional factors and caveats will likely only further refine the overall model that we have outlined here.
DPP6 is a large multi-domain protein so it is perhaps not surprising that it has other functional roles in the nervous system beyond regulation of ISA. DPP6 is closely related to another inactive protease DPP10, and together they make up the DPL (dipeptidyl peptidase-like) gene family. Because DPP10 is not expressed in CG cells, our studies have focused on DPP6; however, it is now clear that we need to rethink this gene family in light of our new observations here. While we have identified many ways in vitro in which DPP6 can alter Kv4 channel expression and function, the exact importance of any given mechanism in vivo is less clear , , , , , , , . With regards to K2P channels, additional experiments are in order. Although knockdown of DPP6 dramatically lowers Kv4 and K2P currents, it is possible that in CG cells DPP6 expression level is not normally a type of “master rheostat” regulating the level of potassium channel functional expression. For one thing, rescue of mDPP6 RNAi effects by DPP6 over expression returns ISA and IK(SO) back to their normal level, suggesting some other factors normally control the levels of these currents . Indeed, we find that over expression of TASK-3 greatly increases the resting membrane conductance suggesting the resting level of IK(SO) is limited by K2P channel expression and not the level of DPP6. Thus, it seems likely that in CG cell DPP6 expression is not normally limiting, although it is possible that over expressed TASK-3 escapes normal controls on expression level.
Multiple distinct N-terminal variants of DPP6 are produced in CG cells through the use of alternative promoters in the DPP6 gene . Heterologous expression studies show that these DPP6 N-terminal variants differentially regulate Kv4 channel function, providing an alternative mechanism for DPP6 to differentially regulate neuronal function , , , , . In this study we have found differential effects of DPP6a and DPP6K on the resting membrane potential and input resistance of CG cells (see Fig. 2A,B). Future studies will need to determine the importance of differential DPP6 variant expression in shaping neuronal excitability properties of CG cells and other neurons.
Several recent studies have emphasized the potential links between DPL genes and human disease processes. Human genetic linkage studies have linked DPL genetic variations to asthma, amyotrophic lateral sclerosis, ventricular fibrillations, cancer, craniofacial disorders, and autism spectrum disorders , , , , , , , , , . Interestingly, some of these disorders, including cancer, facial dysmorphisms, and mental retardation have been linked to K2P channels but not Kv4 channels , , . Whether these diseases are caused by DPL dysregulation of K2P or Kv4 channels or some other as yet unidentified function of DPL proteins is not known. However, it is now clear that a better understanding of the roles of DPL proteins in health and disease will require a more complete understanding of how DPL proteins function beyond just the regulation of Kv4 channels.
Finally, as part of a functional network, neurons must strike a balance between relaying and retaining incoming information. Our studies suggest that in CG cells DPP6 expression pushes this balance towards more retaining and internal processing of incoming information. In the absence of DPP6, CG cells are much more likely to relay information since the neuron reaches threshold more easily in response to excitatory inputs and thus most input spikes will generate output spikes with a minimal change in the information content. In the presence of DPP6, the same inputs are more likely to be retained and encoded as dynamic changes in the inactivation state of ISA channels with only the strongest inputs producing action potential firing. Thus the incoming information is transformed into patterns of ISA channel inactivation in a way that is tuned by DPP6 effects on ISA channel steady state and kinetic gating properties as well as effects on resting membrane properties. Ultimately these changes in ISA channel gating will dynamically affect the function of the entire network by altering neuronal excitability, and synaptic strengths by regulating action potential backpropagation , . It will be interesting in future studies in vivo to determine how changes in the expression patterns for DPP6, and DPP6 variants, affect how neurons process information, and whether these effects are modulated by the differential expression of other channel components.
Fits of ISA gating models to the Data. Currents for ISA models under Control (GISA(c)) and mDPP6 RNAi (GISA(r)) treatment conditions are compared to our published properties for CG cell ISA recorded under the same conditions . Symbols are data taken from our published CG cell recordings. Solid curves (B, C, D) were generated by our GISA(c) and GISA(r) models. A) Representative currents in response to a step to 6 mV. Symbols- average peak current recorded from CG cells under these conditions. Model currents (black) are compared to recorded currents (red) (recorded currents scaled to facilitate comparison of inactivation kinetics). B) Fits to ISA steady state inactivation and peak activation data. C) Recovery data for CG cell ISA. D) Time to peak data for CG cell ISA. E) Histogram showing distribution of fast inactivation taus recorded with strong depolarizations >40 mV. Vertical lines show the measured fast inactivation taus for our GISA(c) and GISA(r) models at 50 mV.
Thanks to Melissa Schaefer for technical assistance, and Dr. Henry Jerng for useful discussions and help preparing this manuscript.
Conceived and designed the experiments: BMN PJP. Performed the experiments: BMN. Analyzed the data: BMN PJP. Contributed reagents/materials/analysis tools: BMN PJP. Wrote the paper: BMN PJP.
- 1. Ito M (2008) Control of mental activities by internal models in the cerebellum. Nat Rev Neurosci 9: 304–313. doi: 10.1038/nrn2332
- 2. Napper RM, Harvey RJ (1988) Number of parallel fiber synapses on an individual Purkinje cell in the cerebellum of the rat. J Comp Neurol 274: 168–177. doi: 10.1002/cne.902740204
- 3. Nadal MS, Ozaita A, Amarillo Y, de Miera EV, Ma Y, et al. (2003) The CD26-related dipeptidyl aminopeptidase-like protein DPPX is a critical component of neuronal A-type K+ channels. Neuron 37: 449–461. doi: 10.1016/s0896-6273(02)01185-6
- 4. Ren X, Hayashi Y, Yoshimura N, Takimoto K (2005) Transmembrane interaction mediates complex formation between peptidase homologues and Kv4 channels. Mol Cell Neurosci 29: 320–332. doi: 10.1016/j.mcn.2005.02.003
- 5. Jerng HH, Pfaffinger PJ (2012) Incorporation of DPP6a and DPP6K Variants in Ternary Kv4 Channel Complex Reconstitutes Properties of A-type K Current in Rat Cerebellar Granule Cells. PLoS One 7: e38205. doi: 10.1371/journal.pone.0038205
- 6. Nadin BM, Pfaffinger PJ (2010) Dipeptidyl peptidase-like protein 6 is required for normal electrophysiological properties of cerebellar granule cells. J Neurosci 30: 8551–8565. doi: 10.1523/jneurosci.5489-09.2010
- 7. Kim J, Nadal M, Clemens AM, Baron M, Jung SC, et al. (2008) The Kv4 accessory protein DPPX is a critical regulator of membrane excitability in hippocampal CA1 pyramidal neurons. J Neurophysiol 100: 1835–1847. doi: 10.1152/jn.90261.2008
- 8. Watkins CS, Mathie A (1996) A non-inactivating K+ current sensitive to muscarinic receptor activation in rat cultured cerebellar granule neurons. J Physiol 491 (Pt 2): 401–412.
- 9. Han J, Truell J, Gnatenco C, Kim D (2002) Characterization of four types of background potassium channels in rat cerebellar granule neurons. J Physiol 542: 431–444. doi: 10.1113/jphysiol.2002.017590
- 10. Brickley SG, Aller MI, Sandu C, Veale EL, Alder FG, et al. (2007) TASK-3 two-pore domain potassium channels enable sustained high-frequency firing in cerebellar granule neurons. J Neurosci 27: 9329–9340. doi: 10.1523/jneurosci.1427-07.2007
- 11. Cotten JF, Zou HL, Liu C, Au JD, Yost CS (2004) Identification of native rat cerebellar granule cell currents due to background K channel KCNK5 (TASK-2). Brain Res Mol Brain Res 128: 112–120. doi: 10.1016/j.molbrainres.2004.06.007
- 12. Millar JA, Barratt L, Southan AP, Page KM, Fyffe RE, et al. (2000) A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons. Proc Natl Acad Sci U S A 97: 3614–3618. doi: 10.1073/pnas.97.7.3614
- 13. Ketchum KA, Joiner WJ, Sellers AJ, Kaczmarek LK, Goldstein SA (1995) A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. Nature 376: 690–695. doi: 10.1038/376690a0
- 14. Kollewe A, Lau AY, Sullivan A, Roux B, Goldstein SA (2009) A structural model for K2P potassium channels based on 23 pairs of interacting sites and continuum electrostatics. J Gen Physiol 134: 53–68. doi: 10.1085/jgp.200910235
- 15. Brohawn SG, del Marmol J, MacKinnon R (2012) Crystal structure of the human K2P TRAAK, a lipid- and mechano-sensitive K+ ion channel. Science 335: 436–441. doi: 10.1126/science.1213808
- 16. Clarke CE, Veale EL, Green PJ, Meadows HJ, Mathie A (2004) Selective block of the human 2-P domain potassium channel, TASK-3, and the native leak potassium current, IKSO, by zinc. J Physiol 560: 51–62. doi: 10.1113/jphysiol.2004.070292
- 17. Aller MI, Veale EL, Linden AM, Sandu C, Schwaninger M, et al. (2005) Modifying the subunit composition of TASK channels alters the modulation of a leak conductance in cerebellar granule neurons. J Neurosci 25: 11455–11467. doi: 10.1523/jneurosci.3153-05.2005
- 18. Lopes CM, Rohacs T, Czirjak G, Balla T, Enyedi P, et al. (2005) PIP2 hydrolysis underlies agonist-induced inhibition and regulates voltage gating of two-pore domain K+ channels. J Physiol 564: 117–129. doi: 10.1113/jphysiol.2004.081935
- 19. Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, et al. (1997) TASK, a human background K+ channel to sense external pH variations near physiological pH. EMBO J 16: 5464–5471. doi: 10.1093/emboj/16.17.5464
- 20. Aller MI, Wisden W (2008) Changes in expression of some two-pore domain potassium channel genes (KCNK) in selected brain regions of developing mice. Neuroscience 151: 1154–1172. doi: 10.1016/j.neuroscience.2007.12.011
- 21. Berg AP, Talley EM, Manger JP, Bayliss DA (2004) Motoneurons express heteromeric TWIK-related acid-sensitive K+ (TASK) channels containing TASK-1 (KCNK3) and TASK-3 (KCNK9) subunits. J Neurosci 24: 6693–6702. doi: 10.1523/jneurosci.1408-04.2004
- 22. Hines ML, Carnevale NT (2001) NEURON: a tool for neuroscientists. Neuroscientist 7: 123–135. doi: 10.1177/107385840100700207
- 23. Destexhe A, Rudolph M, Fellous JM, Sejnowski TJ (2001) Fluctuating synaptic conductances recreate in vivo-like activity in neocortical neurons. Neuroscience 107: 13–24. doi: 10.1016/s0306-4522(01)00344-x
- 24. D’Angelo E, Nieus T, Maffei A, Armano S, Rossi P, et al. (2001) Theta-frequency bursting and resonance in cerebellar granule cells: experimental evidence and modeling of a slow k+-dependent mechanism. J Neurosci 21: 759–770.
- 25. Milescu LS, Akk G, Sachs F (2005) Maximum likelihood estimation of ion channel kinetics from macroscopic currents. Biophys J 88: 2494–2515. doi: 10.1529/biophysj.104.053256
- 26. Jerng H, Dougherty K, Covarrubias M, Pfaffinger PJ (2009) A novel N-terminal motif of dipeptidyl peptidase-like proteins produces rapid inactivation of Kv4.2 channels by a pore-blocking mechanism. Channels 3: 448–461. doi: 10.4161/chan.3.6.10216
- 27. Ashmole I, Vavoulis DV, Stansfeld PJ, Mehta PR, Feng JF, et al. (2009) The response of the tandem pore potassium channel TASK-3 (K(2P)9.1) to voltage: gating at the cytoplasmic mouth. J Physiol 587: 4769–4783. doi: 10.1113/jphysiol.2009.175430
- 28. Chen X, Yuan LL, Zhao C, Birnbaum SG, Frick A, et al. (2006) Deletion of Kv4.2 gene eliminates dendritic A-type K+ current and enhances induction of long-term potentiation in hippocampal CA1 pyramidal neurons. J Neurosci 26: 12143–12151. doi: 10.1523/jneurosci.2667-06.2006
- 29. Menegola M, Trimmer JS (2006) Unanticipated region- and cell-specific downregulation of individual KChIP auxiliary subunit isotypes in Kv4.2 knock-out mouse brain. J Neurosci 26: 12137–12142. doi: 10.1523/jneurosci.2783-06.2006
- 30. Norris AJ, Foeger NC, Nerbonne JM (2010) Interdependent roles for accessory KChIP2, KChIP3, and KChIP4 subunits in the generation of Kv4-encoded IA channels in cortical pyramidal neurons. J Neurosci 30: 13644–13655. doi: 10.1523/jneurosci.2487-10.2010
- 31. Foeger NC, Norris AJ, Wren LM, Nerbonne JM (2012) Augmentation of Kv4.2-encoded currents by accessory dipeptidyl peptidase 6 and 10 subunits reflects selective cell surface Kv4.2 protein stabilization. J Biol Chem 287: 9640–9650. doi: 10.1074/jbc.m111.324574
- 32. Nerbonne JM, Gerber BR, Norris A, Burkhalter A (2008) Electrical remodelling maintains firing properties in cortical pyramidal neurons lacking KCND2-encoded A-type K+ currents. J Physiol 586: 1565–1579. doi: 10.1113/jphysiol.2007.146597
- 33. Nadal MS, Amarillo Y, Vega-Saenz de Miera E, Rudy B (2006) Differential characterization of three alternative spliced isoforms of DPPX. Brain Res 1094: 1–12. doi: 10.1016/j.brainres.2006.03.106
- 34. Maffie J, Blenkinsop T, Rudy B (2009) A novel DPP6 isoform (DPP6-E) can account for differences between neuronal and reconstituted A-type K(+) channels. Neurosci Lett 449: 189–194. doi: 10.1016/j.neulet.2008.10.098
- 35. Lazarenko RM, Willcox SC, Shu S, Berg AP, Jevtovic-Todorovic V, et al. (2010) Motoneuronal TASK channels contribute to immobilizing effects of inhalational general anesthetics. J Neurosci 30: 7691–7704. doi: 10.1523/jneurosci.1655-10.2010
- 36. Diwakar S, Magistretti J, Goldfarb M, Naldi G, D’Angelo E (2009) Axonal Na+ channels ensure fast spike activation and back-propagation in cerebellar granule cells. J Neurophysiol 101: 519–532. doi: 10.1152/jn.90382.2008
- 37. Lugo JN, Brewster AL, Spencer CM, Anderson AE (2012) Kv4.2 knockout mice have hippocampal-dependent learning and memory deficits. Learn Mem 19: 182–189. doi: 10.1101/lm.023614.111
- 38. Watanabe S, Hoffman DA, Migliore M, Johnston D (2002) Dendritic K+ channels contribute to spike-timing dependent long-term potentiation in hippocampal pyramidal neurons. Proc Natl Acad Sci U S A 99: 8366–8371. doi: 10.1073/pnas.122210599
- 39. Johnston D, Christie BR, Frick A, Gray R, Hoffman DA, et al. (2003) Active dendrites, potassium channels and synaptic plasticity. Philos Trans R Soc Lond B Biol Sci 358: 667–674. doi: 10.1098/rstb.2002.1248
- 40. Andrasfalvy BK, Makara JK, Johnston D, Magee JC (2008) Altered synaptic and non-synaptic properties of CA1 pyramidal neurons in Kv4.2 KO mice. J Physiol 586: 3881–3892. doi: 10.1113/jphysiol.2008.154336
- 41. Dan Y, Poo MM (2004) Spike timing-dependent plasticity of neural circuits. Neuron 44: 23–30. doi: 10.1016/j.neuron.2004.09.007
- 42. Pongs O, Schwarz JR (2010) Ancillary subunits associated with voltage-dependent K+ channels. Physiol Rev 90: 755–796. doi: 10.1152/physrev.00020.2009
- 43. Marionneau C, Carrasquillo Y, Norris AJ, Townsend RR, Isom LL, et al. (2012) The sodium channel accessory subunit Navbeta1 regulates neuronal excitability through modulation of repolarizing voltage-gated K(+) channels. J Neurosci 32: 5716–5727. doi: 10.1523/jneurosci.6450-11.2012
- 44. Carrion AM, Link WA, Ledo F, Mellstrom B, Naranjo JR (1999) DREAM is a Ca2+-regulated transcriptional repressor. Nature 398: 80–84. doi: 10.1038/18044
- 45. Xia XM, Fakler B, Rivard A, Wayman G, Johnson-Pais T, et al. (1998) Mechanism of calcium gating in small-conductance calcium-activated potassium channels. Nature 395: 503–507. doi: 10.1038/26758
- 46. Erickson MG, Alseikhan BA, Peterson BZ, Yue DT (2001) Preassociation of calmodulin with voltage-gated Ca(2+) channels revealed by FRET in single living cells. Neuron 31: 973–985. doi: 10.1016/s0896-6273(01)00438-x
- 47. Zheng J, Varnum MD, Zagotta WN (2003) Disruption of an intersubunit interaction underlies Ca2+-calmodulin modulation of cyclic nucleotide-gated channels. J Neurosci 23: 8167–8175.
- 48. Soh H, Goldstein SA (2008) ISA channel complexes include four subunits each of DPP6 and Kv4.2. J Biol Chem 283: 15072–15077. doi: 10.1074/jbc.m706964200
- 49. Amarillo Y, De Santiago-Castillo JA, Dougherty K, Maffie J, Kwon E, et al. (2008) Ternary Kv4.2 channels recapitulate voltage-dependent inactivation kinetics of A-type K+ channels in cerebellar granule neurons. J Physiol 586: 2093–2106. doi: 10.1113/jphysiol.2007.150540
- 50. Jerng HH, Qian Y, Pfaffinger PJ (2004) Modulation of Kv4.2 Channel Expression and Gating by Dipeptidyl Peptidase 10 (DPP10). Biophys J 87: 2380–2396. doi: 10.1529/biophysj.104.042358
- 51. Sun W, Maffie JK, Lin L, Petralia RS, Rudy B, et al. (2011) DPP6 establishes the A-type K(+) current gradient critical for the regulation of dendritic excitability in CA1 hippocampal neurons. Neuron 71: 1102–1115. doi: 10.1016/j.neuron.2011.08.008
- 52. Molineux ML, Fernandez FR, Mehaffey WH, Turner RW (2005) A-type and T-type currents interact to produce a novel spike latency-voltage relationship in cerebellar stellate cells. J Neurosci 25: 10863–10873. doi: 10.1523/jneurosci.3436-05.2005
- 53. Anderson D, Rehak R, Hameed S, Mehaffey WH, Zamponi GW, et al. (2010) Regulation of the KV4.2 complex by CaV3.1 calcium channels. Channels 4: 163–167. doi: 10.4161/chan.4.3.11955
- 54. Duguid I, Branco T, London M, Chadderton P, Hausser M (2012) Tonic inhibition enhances fidelity of sensory information transmission in the cerebellar cortex. J Neurosci 32: 11132–11143. doi: 10.1523/jneurosci.0460-12.2012
- 55. Jerng HH, Kunjilwar K, Pfaffinger PJ (2005) Multiprotein assembly of Kv4.2, KChIP3 and DPP10 produces ternary channel complexes with ISA-like properties. J Physiol 568: 767–788. doi: 10.1113/jphysiol.2005.087858
- 56. Dougherty K, Covarrubias M (2006) A dipeptidyl aminopeptidase-like protein remodels gating charge dynamics in Kv4.2 channels. J Gen Physiol 128: 745–753. doi: 10.1085/jgp.200609668
- 57. Seikel E, Trimmer JS (2009) Convergent modulation of Kv4.2 channel alpha subunits by structurally distinct DPPX and KChIP auxiliary subunits. Biochemistry 48: 5721–5730. doi: 10.1021/bi802316m
- 58. Jerng HH, Lauver AD, Pfaffinger PJ (2007) DPP10 splice variants are localized in distinct neuronal populations and act to differentially regulate the inactivation properties of Kv4-based ion channels. Mol Cell Neurosci 35: 604–624. doi: 10.1016/j.mcn.2007.03.008
- 59. van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, et al. (2008) Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nat Genet 40: 29–31. doi: 10.1038/ng.2007.52
- 60. Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, et al. (2008) Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 82: 477–488. doi: 10.1016/j.ajhg.2007.12.009
- 61. Cronin S, Berger S, Ding J, Schymick JC, Washecka N, et al. (2008) A genome-wide association study of sporadic ALS in a homogenous Irish population. Hum Mol Genet 17: 768–774. doi: 10.1093/hmg/ddm361
- 62. Schade J, Stephan M, Schmiedl A, Wagner L, Niestroj AJ, et al. (2008) Regulation of expression and function of dipeptidyl peptidase 4 (DP4), DP8/9, and DP10 in allergic responses of the lung in rats. J Histochem Cytochem 56: 147–155. doi: 10.1369/jhc.7a7319.2007
- 63. Allen M, Heinzmann A, Noguchi E, Abecasis G, Broxholme J, et al. (2003) Positional cloning of a novel gene influencing asthma from chromosome 2q14. Nat Genet 35: 258–263. doi: 10.1038/ng1256
- 64. Jones S, Zhang X, Parsons DW, Lin JC, Leary RJ, et al. (2008) Core signaling pathways in human pancreatic cancers revealed by global genomic analyses. Science 321: 1801–1806. doi: 10.1126/science.1164368
- 65. Low SK, Kuchiba A, Zembutsu H, Saito A, Takahashi A, et al. (2010) Genome-wide association study of pancreatic cancer in Japanese population. PLoS One 5: e11824. doi: 10.1371/journal.pone.0011824
- 66. Fan Z, Du J, Liu H, Zhang H, Dlugosz AA, et al. (2009) A susceptibility locus on 1p32–1p34 for congenital macrostomia in a Chinese family and identification of a novel PTCH2 mutation. Am J Med Genet A 149A: 521–524. doi: 10.1002/ajmg.a.32647
- 67. Du J, Fan Z, Ma X, Gao Y, Wu Y, et al. (2011) Expression of Dpp6 in mouse embryonic craniofacial development. Acta Histochem 113: 636–639. doi: 10.1016/j.acthis.2010.08.001
- 68. Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, et al. (2009) Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation. Am J Hum Genet 84: 468–476. doi: 10.1016/j.ajhg.2009.02.009
- 69. Mu D, Chen L, Zhang X, See LH, Koch CM, et al. (2003) Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene. Cancer Cell 3: 297–302. doi: 10.1016/s1535-6108(03)00054-0
- 70. Barel O, Shalev SA, Ofir R, Cohen A, Zlotogora J, et al. (2008) Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9. Am J Hum Genet 83: 193–199. doi: 10.1016/j.ajhg.2008.07.010
- 71. Es-Salah-Lamoureux Z, Steele DF, Fedida D (2010) Research into the therapeutic roles of two-pore-domain potassium channels. Trends Pharmacol Sci 31: 587–595. doi: 10.1016/j.tips.2010.09.001
- 72. Hoffman DA, Magee JC, Colbert CM, Johnston D (1997) K+ channel regulation of signal propagation in dendrites of hippocampal pyramidal neurons. Nature 387: 869–875. doi: 10.1038/43119
- 73. Hille B (2001) Ion Channels of Excitable Membranes. Sunderland, MA: Sinauer Associates Inc. 814 p.