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¹ Department of Anatomy and Neurobiology, University of Tennessee, 855 Monroe Avenue, Memphis, TN 38163, USA
² Department of Physiology, Northwestern University, 745 N. Fairbanks Court, Chicago, IL 60611, USA

	Abstract

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We determined the expression of Kv2 channel subunits in rat somatosensory and motor cortex and tested for the contributions of Kv2 subunits to slowly inactivating K⁺ currents in supragranular pyramidal neurons. Single cell RT-PCR showed that virtually all pyramidal cells expressed Kv2.1 mRNA and 80% expressed Kv2.2 mRNA. Immunocytochemistry revealed striking differences in the distribution of Kv2.1 and Kv2.2 subunits. Kv2.1 subunits were clustered and located on somata and proximal dendrites of all pyramidal cells. Kv2.2 subunits were primarily distributed on large apical dendrites of a subset of pyramidal cells from deep layers. We used two methods for isolating currents through Kv2 channels after excluding contributions from Kv1 subunits: intracellular diffusion of Kv2.1 antibodies through the recording pipette and extracellular application of rStromatoxin-1 (ScTx). The Kv2.1 antibody specifically blocked the slowly inactivating K⁺ current by 25–50% (at 8 min), demonstrating that Kv2.1 subunits underlie much of this current in neocortical pyramidal neurons. ScTx (300 nM) also inhibited 40% of the slowly inactivating K⁺ current. We observed occlusion between the actions of Kv2.1 antibody and ScTx. In addition, Kv2.1 antibody- and ScTx-sensitive currents demonstrated similar recovery from inactivation and voltage dependence and kinetics of activation and inactivation. These data indicate that both agents targeted the same channels. Considering the localization of Kv2.1 and 2.2 subunits, currents from truncated dissociated cells are probably dominated by Kv2.1 subunits. Compared with Kv2.1 currents in expression systems, the Kv2.1 current in neocortical pyramidal cells activated and inactivated at relatively negative potentials and was very sensitive to holding potential.

(Received 17 January 2007; accepted after revision 15 March 2007; first published online 22 March 2007)
Corresponding author R. C. Foehring: Department of Anatomy and Neurobiology, University of Tennessee, 855 Monroe Avenue, Memphis, TN 38163, USA. Email: rfoehrin{at}utmem.edu

	Introduction

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Voltage-gated potassium channels (Kv) are extremely diverse, with 12 known subfamilies of Kv channels (Coetzee et al. 1999). They play pivotal roles in regulating neuronal excitability, shaping action potentials, and modulating spike patterns (Hille, 2000). Relationships between specific channel subunits and native potassium currents are poorly understood, however. Channel subunits responsible for voltage-gated potassium currents in neurons have been identified in very few cases (e.g. Wang et al. 1998; Murakoshi & Trimmer, 1999; Du et al. 2000; Malin & Nerbonne, 2002; Yuan et al. 2005). Knowledge of such molecular correlations is needed to understand modulation of K⁺ currents by neurotransmitters and K⁺ channel-related pathophysiology (cf. McCormick et al. 1993; Wible et al. 1997; Wickenden, 2002).

On the basis of biophysical properties (especially inactivation kinetics) and sensitivity to TEA and 4-AP, voltage-gated K⁺ currents in pyramidal neurons are typically divided into I_A, I_M, I_K, and I_D (Storm, 1990; Zhou & Hablitz, 1996; Locke & Nerbonne, 1997;Bekkers, 2000a,b; Korngreen & Sakmann, 2000). I_A is a rapidly activating, rapidly inactivating current. I_M is a very slowly activating and deactivating and non-inactivating current that is highly sensitive to muscarinic agonists (Brown & Adams, 1980). I_D was originally described as a slowly inactivating, 4-AP-sensitive current that was very sensitive to holding potential (Storm, 1988). The most common current definition of I_D is the current sensitive to -dendrotoxin (-DTX; Wu & Barish, 1992; Bekkers, 2000a,b; Korngreen & Sakmann, 2000; reviewed in Guan et al. 2006). I_K is also referred to as the delayed rectifier current (I_DR: Zhou & Hablitz, 1996). This slowly inactivating current activates more slowly than I_A and I_D but more rapidly than I_M and is variably TEA sensitive.

Classification of K⁺ currents on the basis of biophysics and/or TEA and 4-AP sensitivities has proven unsatisfactory for many reasons. Besides the differing definitions of I_D, the slowly inactivating current has complicated kinetics, voltage dependence and pharmacology (Foehring & Surmeier, 1993). A more natural classification system is preferable, based upon the underlying channel subunits.

Expression of Kv subunits in expression systems has revealed a great deal about the properties of specific subunits but we have only limited knowledge of the contributions of these subunits to currents in native neuronal membranes. We previously used single cell RT-PCR, immunocytochemistry, and recordings with specific peptide toxins to demonstrate that layer II/III pyramidal cells express several Kv1 subunits (Kv1.1–1.4: Guan et al. 2006). -DTX blocks channels containing Kv1.1, 1.2 and 1.6 subunits. The -DTX-sensitive current made up 10% of the slowly inactivating current from negative holding potentials (Guan et al. 2006). What channel subunits underlie the remaining 90% of the current? Two major candidates are Kv2 and Kv7 family subunits.

In sympathetic neurons, I_M is due to heteromultimeric expression of Kv7 subunits (Wang et al. 1998; Selyanko et al. 2002; Shah et al. 2002). Kv2.1 is ubiquitously expressed throughout the mammalian brain with the most abundant expression on somata and proximal dendritic processes of pyramidal cells in cerebral cortex and hippocampus (Frech et al. 1989; Trimmer, 1991; Hwang et al. 1993; Du et al. 1998). In cultured hippocampal pyramidal neurons, the sustained outward potassium current is greatly reduced by intracellular diffusion of polyclonal Kv2.1 antibodies or by antisense treatment against Kv2.1, indicating that Kv2.1 is a major contributor to the delayed rectifier currents (Murakoshi & Trimmer, 1999: Du et al. 2000). Intracellular application of the Kv2.1 antibody also demonstrated Kv2.1 involvement in smooth muscle (Archer et al. 1998; Lu et al. 2002). Transient over-expression of dominant-negative Kv2 subunits in embryonic or perinatal neurons demonstrated that native Kv2 subunits contribute to the sustained or slowly activating potassium currents in many cell types (e.g. Kv2.2 in spinal neurons: Blaine & Ribera, 2001; Kv2.1 and Kv2.2 in rat superior cervical ganglion sympathetic neurons: Malin & Nerbonne, 2002; Kv2.1 in pancreatic cells: MacDonald et al. 2002). We hypothesized that Kv2 channels underlie most of the slowly inactivating potassium current in layer II/III neocortical pyramidal neurons.

We found expression of Kv2.1 and Kv2.2 mRNA and channel proteins in neocortical pyramidal neurons. We isolated currents through Kv2 channels by including Kv2.1 antibodies in the recording pipette and by extracellular administration of a peptide gating modifier of Kv2, rStromatoxin-1 (ScTx: Escoubas et al. 2002). The Kv2.1-mediated current was the dominant current in layer II/III pyramidal cells. We characterized the biophysical properties of these currents.

	Methods

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Tissue preparation

These studies were performed on juvenile rats (Sprague–Dawley, postnatal day 16–42 (P16–42)). All procedures were approved by the Animal Care and Use Committee, University of Tennessee, Health Science Center. Briefly, the animal was placed into a sealed plastic container into which gauze soaked with isofluorane was placed under a fibreglass screen floor. The animals were anaesthetized with isofluorane until the animal was areflexive. After anaesthesia with isoflurane, the animals were decapitated and the brain was removed and held in ice-cold cutting solution for 30–60 s. The cutting solution contained (mM): 250 sucrose, 25 KCl, 1 NaH₂PO₄, 11 glucose, 4 MgSO₄, 0.1 CaCl₂, 15 Hepes (pH 7.3–7.4; 300 mosmol l^–1). Coronal slices 400 µm thick of the fronto-parietal regions were cut using a vibrating tissue slicer (World Precision Instruments, Sarasota, FL, USA). The slices were then transferred to a mesh surface in a chamber containing artificial cerebrospinal fluid (aCSF), which was continuously bubbled with a 95% O₂–5% CO₂ (carbogen) mixture at room temperature (RT). The aCSF contained (mM): 125 NaCl, 3 KCl, 2 CaCl₂, 2 MgCl₂, 1.25 NaH₂PO₄, 26 NaHCO₃, and 20 glucose (pH 7.4; 310 mosmol l^–1).

Acute isolation of neurons

The supragranular layers (I–III) or deep layers (V/VI) of primary motor and primary somatosensory cortex were dissected into 3-mm-wide pieces from brain slices under a stereomicroscope. Four to ten tissue pieces were then transferred to oxygenated aCSF (35°C) with added enzyme (Sigma Protease type XIV, 1.2 mg ml^–1: Sigma Chemicals, St Louis, MO, USA). After 12–30 min of incubation in enzyme, the tissue pieces were washed with sodium isethionate solution, which consisted of (mM): 140 sodium isethionate, 2 KCl, 4 MgCl₂, 23 glucose, 15 Hepes (pH 7.3; 300 mosmol l^–1). This solution and enzyme-treated tissue pieces were triturated using three successively smaller fire-polished pipettes to release individual neuronal somata. The supernatant from each trituration step was collected and transferred to a fresh container and plated onto a plastic Petri dish (Nunc, Rochester, NY, USA) on an inverted microscope stage. After 5–8 min of settling time, a uniform background flow of 1 ml min^–1 of Hepes-buffered saline solution (HBSS) was established. HBSS consisted of (mM): 138 NaCl, 3 KCl, 1 MgCl₂, 2 CaCl₂, 10 Hepes, 10–20 dextrose (pH 7.3; 300–305 mosmol l^–1).

Electrophysiology

Whole cell patch clamp recordings were performed on 110 acutely dissociated pyramidal neurons (56 from P27–P36, 43 from P21–P26, 11 from P16–P20). A multibarrel array of glass capillaries (500 µm outer diameter) was used to apply external recording solutions. Solutions were changed by moving the active barrel (from which the solution flows) to surround the recorded cell. To isolate K⁺ current for recording, the external solution contained (mM): 140 sodium isethionate, 3 KCl, 1 MgCl₂, 12 glucose, 10 Hepes, and 1.5 CaCl₂, plus 1 µM tetrodotoxin (TTX) and 100–400 µM CdCl₂ for blocking Na⁺ and Ca²⁺ channels, respectively. A few experiments were performed in the absence of Cd²⁺, to test for its effects on K⁺ current components. The following peptide toxins were used individually or jointly in the external solution for blocking specific Kv channels: -dendrotoxin (-DTX: 100–200 nM to block Kv1.1, 1.2 and 1.6), rMargatoxin (MTX: 10–20 nM to block Kv1.3), and rStromatoxin-1 (ScTx: 100–1000 nM to block Kv2.1, Kv2.2 and Kv4.2). BSA (0.1%) was added to all solutions to prevent peptides from binding to glass and plastic vessels. All peptide toxins were obtained from Alomone Laboratories (Alomone Laboratories, Ltd, Jerusalem, Israel). In some experiments, TEA was included in external solutions, with the concentration of sodium isethionate accordingly reduced to maintain an osmolality of 300 mosmol l^–1.

Recordings were made with a DAGAN 8900 (Minneapolis, MN, USA) amplifier at room temperature (21–23°C). Corning 7052 capillary glass (Garner Glass: Claremont, CA, USA) was used to create electrodes on a Sutter Instruments (Novato, CA, USA) Model P-87 Flaming/Brown micropipette puller. Electrodes were fire-polished and filled with internal solution. The internal solution consisted of (mM): 86 KMeSO₄, 54 KOH, 2 MgCl₂, 40 Hepes, 2 adenosine triphosphate disodium (ATP), 0.2 guanosine 5'-triphosphate sodium salt (GTP), 9 creatine phosphate, 0.1 leupeptin, 10 BAPTA (pH 7.2; 270 mosmol l^–1). Electrode resistances were 1.4–2.2 M. Series resistance was usually compensated by 70–90%. Cells with calculated series resistance errors of > 5 mV were discarded (series resistance error (mV) = series resistance after compensation (G) multiplied by peak current (pA)). Membrane potentials were corrected for the measured liquid junctional potential (+8 mV). Data acquisition (20 kHz sampling, filtered at 5 kHz) and analysis were done using pCLAMP 8 software (Axon Instruments, Union City, CA, USA) and Prism 4 (GraphPad Software, Inc., San Diego, CA, USA). Linear leak currents and capacitative artifacts were subtracted using an online P/4 or P/6 protocol.

For the experiments using intracellular antibodies, the pipettes were dipped in an antibody-free internal solution and then back filled with the internal solution containing the antibodies of interest. We applied monoclonal and polyclonal antibodies to the Kv2.1 C-terminus (monoclonal: AAs 509–853; polyclonal: AAs 837–853: Trimmer, 1991; Misonou et al. 2005) intracellularly to 49 cells (6 cells: P16–P20, 43 cells P21–33). Polyclonal antibodies were obtained from Alamone Laboratories. Monoclonal Kv2.1 antibodies were initially obtained from Upstate, and more recently from Neuromab (Davis, CA, USA). Similar results were obtained with both polyclonal and monoclonal antibodies from all of these sources. Kv2.1 antibody concentration in the internal solution was 8–10 µg ml^–1 or 0.4 µg ml^–1. In control experiments, Kv2.1 antibodies were first mixed with Kv2.1 antigens of the same concentration. After 1 h incubation at room temperature, neutralized Kv2.1 antibodies were added to the internal solution for recording. Effects of polyclonal antibodies to the C-terminus of Kv2.2 (Blaine & Ribera, 1998; obtained from Phosphosolutions: Colorado Biosciences Park, Aurora, CO, USA) were tested in the internal solution at concentration of 1 : 100.

Single cell RT-PCR

Acutely dissociated neurons (layers I–III or V/VI) were harvested for these experiments (9 animals: P28–P37). Pyramidal neurons were identified by shape and the presence of an apical dendrite. Electrode glass (Corning 7052) was autoclaved and heated to 150–200°C for 2 h. After formation of a giga-ohm seal, the cell was lifted up into a stream of HBSS flowing out of the multibarrel array. Suction was increased to aspirate the cell into the pipette. The pipette contained diethylpyrocarbonate-treated (DEPC) water and 0.8 U ml^–1 Superase-In (Ambion, Austin, TX, USA). After aspiration, the pipette tip containing the cell was broken into a 0.6 ml pre-siliconized Midwest Scientific tube (Valley Park, MO, USA) and the contents ejected into the cell collection components for reverse transcription. Eppendorf tubes containing 0.7 µl of SUPERase-In (20 mg l^–1), 1.9 µl of diethylpyrocarbonate-treated water, 1 µl of dNTPs (10 mM), 0.7 µl of BSA (143 mg l^–1) and 0.7 µl of oligo-dT (0.5 mg l^–1) together with cell contents were heated to 65°C for 5 min and then placed on ice for at least 1 min. Single-strand cDNA was synthesized from the cellular mRNA by adding 2 µl of 10x PCR buffer, 4 µl of MgCl₂ (25 mM), 2 µl of DTT (0.1 M), 1 µl of RNase out (40 mg l^–1), 1 µl of Superscript III (50 µg µl^–1) and 6 µl of diethylpyrocarbonate-treated water to the cell. The reverse transcriptase was then incubated at 50°C for 90 min. The reaction was terminated by heating the mixture to 85°C for 5 min. The RNA strand in the RNA–DNA hybrid was then removed by adding 0.5 µl of RNase H (2 µg ml^–1) and incubated at 37°C for 20 min. All reagents except SUPERase-In were obtained from Invitrogen (Gaithersburg, MD, USA). PCR was performed using procedures designed to minimize cross contamination. Negative controls for contamination from extraneous (replace cellular template with water) and genomic DNA (without reverse transcriptase) were run for every batch of neurons. The single cell cDNA generated from the above step was subjected to conventional PCR using a programmable thermal cycler. PCR primers were developed from the GenBank sequences with OLIGO software (v6.6). Primers were for calcium calmodulin kinase II (CamKII), Kv2.1 and Kv2.2 (Baranauskas et al. 1999; Guan et al. 2006). ‘Touchdown’ protocols were implemented for more efficient amplification of single cell DNA: 35 cycles were run at the optimal annealing temperature for each primer set, then the annealing temperature was decreased by 1°C for two cycles, five times, for a total of 45 cycles.

Immunocytochemistry

Animals (n = 8, P26–P42) were anaesthetized with sodium pentobarbital (50 mg kg^–1 I.P.). The anaesthetized animals were transcardially perfused with 0.01 M sodium phosphate buffer plus 0.89% NaCl (PBS) followed by PBS-buffered 4% paraformaldehyde and 0.2% picric acid. Brains were removed, post-fixed for 12 h at 4°C, then blocked and placed in a solution of fixative containing sucrose (30% w/v) for cryoprotection. Sections through the cortex were taken at 40 µm on a freezing microtome, rinsed in PBS, and incubated in 2% normal goat serum with 3% H₂O₂ for 1–2 h to reduce background staining. Antibodies to Kv2.2 subunits were obtained from PhosphoSolutions (Kv2.2; Aurora) or donated by Dr A. Ribera (University of Colorado, Denver). Similar results were obtained with polyclonal (Sigma: n = 2) and monoclonal antibodies (Upstate (Billerica, MA, USA: n = 2) or NeuroMab (UC Davis, CA, USA: n = 4)) to Kv2.1. These were the same antibodies as used for intracellular block of K⁺ currents (see above). Antibodies were tested first at various concentrations (1 : 100 to 1 : 1000) in PBS and 0.5% Triton X-100 (PBS-TX).

ABC staining

After three rinses with PBS-TX, the sections were incubated in biotinylated goat anti-rabbit (GAR-B) or horse anti-mouse (HAM-B) antibodies at 1 : 200 overnight (4°C). After three rinses in PBS-TX, the sections were incubated for 4 h with avidin–biotin–peroxidase (ABC: Vector Laboratories) dissolved in PBS-TX. After three rinses in PBS-TX, the sections were reacted (as per Vector protocol) with Ni²⁺-intensified Diamino benzidine (DAB) (60 mg ml^–1) plus 0.003% H₂O₂ for 5–10 min. The reaction was terminated by several rinses in PBS-TX. The sections were then mounted on gelatin-coated glass slides, dehydrated, coverslipped, and viewed with conventional light microscopy.

Immunofluorescence

Double staining was accomplished using the PhosphoSolutions polyclonal Kv2.2 antibody and the Neuromab monoclonal Kv2.1 antibody diluted in PBS-TX. Following overnight incubation with a cocktail of primary antibodies (1 : 200 to 1 : 400), the sections were incubated overnight in a cocktail of secondary antibodies (1 : 200) consisting of Fluorescein GAR-(FITC) and GOAT anti-mouse (GAM)-AlexaFluor 568 conjugates, all at 4°C. The sections were rinsed in PBS-TX, mounted on gelatin-coated slides, and coverslipped with Vectashield (Vector). These sections were viewed with a Bio-Rad (Hercules, CA, USA) confocal microscope equipped with a krypton–argon laser. FITC was examined with a 488 nm excitation filter (emission bandpass 522 nm), and AlexaFluor 568 was examined with a 568 nm excitation filter (emission bandpass 605 nm). The optical section thickness was 1–2 µm. Sections were viewed singly or in stacks of 5–12 sections using 40, 60 or 100x oil immersion objectives (n.a. 1.35, 1.4 and 1.4, respectively). Confocal images (1024 x 1024 pixels) were acquired as 24-bit colour images and viewed with ImageJ (NIH) software. The final confocal figures were made in Adobe Photoshop, with minimal alteration in dynamic range.

Electron microscopy

For electron microscopy, we used the fixative described above with an additional 0.25–0.5% glutaraldehyde. The brains were sectioned at 50 µm on a vibrating microtome (Leica 1000) into PBS, and no Triton X-100 was used for these protocols. After rinsing, the sections were pre-treated with 0.5% H₂O₂ and 1% sodium borohydride to reduce background staining. Following the reaction, sections were reacted with 1% osmium in PBS for 1 h. Osmicated sections were dehydrated, stained en bloc with 2% uranyl acetate, and embedded in plastic (Spurr's resin, EMS, Fort Washington, PA, USA). Ultrathin (75–80 nm) sections were contrasted with lead citrate and uranyl acetate and viewed at 60–100 kV on a JEOL 2000 transmission electron microscope. With the same ABC localization method described above, penetration of antibodies on the Vibratome section without detergent was less than 5 µm. Digital images (2240 x 2944 pixels) were acquired directly with a Hamamatsu ORCA camera and AMT Advantage (Danvers, MA, USA) software. The final electron microscopic figures were made in Adobe Photoshop, with minimal alteration in dynamic range.

Statistics

Data are presented as mean ± standard error of the mean (S.E.M.). Prism Software (GraphPad, Software, Inc., San Diego, CA, USA) was used for statistical tests of significance. Paired or unpaired t tests were used to compare sample population data throughout. P values < 0.05 were considered to be significantly different. Multiple comparisons used one-way ANOVA with Tukey's multiple comparison test for post hoc comparison of means. Sample population data are represented as scatter plots or as box plots (Tukey, 1977). Box plots indicate the upper and lower quartiles as edges of the box, with the median represented as a line crossing the box. The stems indicate the largest and smallest non-outlying values, and outliers are indicated by open circles. Outlying values are greater than 1.5 times the quartile boundaries.

	Results

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Kv2.1 mRNA and Kv2.2 mRNA were expressed in pyramidal cells

Single cell RT-PCR experiments were performed to determine whether pyramidal cells expressed Kv2.1 or Kv2.2 mRNA (9 animals, P28–P37). A primer for Ca²⁺ calmodulin kinase II (CamKII), a specific marker of pyramidal cells in cortex (Jones et al. 1994), was used to confirm the identity of the neurons as pyramidal (Fig. 1). All cells were CamKII positive. In layers II/III, Kv2.1 mRNA was detected in 52/53 (98%), and Kv2.2 mRNA was detected in 42/53 cells (79%, Fig. 1B). In deep layer pyramidal neurons (V/VI), Kv2.1 mRNA was detected in 17/20 cells (85%) and Kv2.2 mRNA detected in 12/20 (60%, Fig. 1B).

View larger version (20K): [in this window] [in a new window]   Figure 1.  Single cell RT-PCR A, gel for a single layer II/III pyramidal cell from a P28 rat. This cell expressed mRNA for CamKII (marker for pyramidal cells), Kv2.1 and Kv2.2. STD, standards. B, histograms to show population data for Kv2 mRNA. Numbers above bars = number of cells. Virtually all pyramidal cells express mRNA for Kv2.1 and most for Kv2.2.

The mRNA data indicated that virtually all pyramidal cells express Kv2.1 mRNA and most express Kv2.2 mRNA. We next used immunocytochemistry to determine whether the corresponding proteins were expressed and if so, in which cell compartments. Kv2.1 subunits were arranged in variably sized clusters on somata and proximal dendrites of the pyramidal cells in both layers II/III (Fig. 2D, stained green) and layer V (Fig. 2A, stained green). In contrast, Kv2.2 proteins were mostly confined to large apical dendrites of a subset of the pyramidal cells in deep layers (Fig. 2B and D, stained red). We were able to connect layer 5 somata with Kv2.2-immunopositive dendrites in many cases, but not layer 2/3 somata (Fig. 2C and D). Little somatic staining was evident in either layer. Electron microscopy indicated that Kv2.2 subunits were found in dendrites and dendritic spines (Fig. 2E). The bulk of the Kv2.2 staining was not associated with the plasma membrane, but rather appeared distributed in vesicular profile throughout the dendrites (Fig. 2F).

View larger version (113K): [in this window] [in a new window]   Figure 2.  Localization of Kv2.1 and Kv2.2 subunits A–C, layer V of somatosensory cortex (P35 rat). Scale bar in B refers to A–C. A, confocal image of single 1 µm section with fluorescent staining for monoclonal anti-Kv2.1 (Neuromab: green). Kv2.1 is patchy and distributed on somata and proximal apical dendrites (mostly < 50 µm from soma) of all pyramidal cells. B, polyclonal anti-Kv2.2 (Phosphosolutions: red) Note Kv2.2 is largely restricted to large dendritic shafts. Arrows point out the same dendrites indicated by arrows in C. C, superimposed Kv2.1 and Kv2.2. In a few cases, Kv2.2-positive (red) dendrites are in continuity with Kv2.1-positive (green) dendrites (e.g. arrows). D, layer 3 of somatosensory cortex (different P35 animal). Confocal image of single 1 µm section with superimposed fluorescent staining for monoclonal anti-Kv2.1 (green) and polyclonal anti-Kv2.2 (red). Kv2.2 stains some dendrites, which are en passant from deeper layers (we could not match layer 3 pyramidal cell somata with anti-Kv2.2-stained dendrites). Scale bar = 20 µm. E, EM image of Kv2.2 localization in dendritic spine (between arrows). F, at the EM level, much of the Kv2.2 staining was within the cytoplasm of pyramidal cell apical dendrites. The staining appeared vesicular (e.g. arrows).

We previously found that 10% of the slowly inactivating current was due to Kv1 subunits (Guan et al. 2006). We now address which subunits underlie the bulk of the current. In all experiments, -DTX and MTX were added to the external solutions to block the Kv1 current. Every 10 s, transmembrane potential was stepped to +10 mV for 200 ms from the holding potential. We determined the TEA dose–response relationship at holding potentials of –80 and –40 mV in the same cell (n = 6, P21–P30). K⁺ currents were tested after the amplitude of the K⁺ currents was stable. Relative block of the current by TEA (at 200 ms) was calculated and was used for fitting the following dose–response curve:

(1)

where I_max is the largest current at 200 ms in the control solution, n_H is the Hill coefficient, and B_max represents the maximum relative block.

As shown in Fig. 3A, almost all of the slowly inactivating current was TEA sensitive. The TEA-sensitive current activated and inactivated slowly. From the –80 mV holding potential, the IC₅₀ for TEA was 10.3 mM (Fig. 3B). When holding potential was increased to –40 mV, 93% of the outward K⁺ current was inactivated (Fig. 3C). The remaining current demonstrated high TEA sensitivity (IC₅₀ = 1.5 mM, Fig. 3D). Therefore, the major outward K⁺ current in the pyramidal cells was TEA sensitive and very sensitive to holding potential (cf. Foehring & Surmeier, 1993).

View larger version (30K): [in this window] [in a new window]   Figure 3.  TEA, Cd2+ and holding potential sensitivities of the outward K+ currents -DTX and MgTX were used in all external solutions to exclude the currents associated with Kv1 channels. Data are presented as mean ± S.E.M. A, example of the K+ current recorded from a holding potential of – 80 mV. 30-mM TEA inhibited a large, slowly activating current component. B, the dose–response relationship for TEA inhibition from holding potential of –80 mV. Over 80% of the outward K+ current was TEA sensitive, with an IC50 of 10.3 mM. nH, Hill coefficient. C, when the holding potential was changed to –40 mV from –80 mV, most outward K+ current was inactivated. *Statistical significance (P < 0.05). D, from a holding potential of –40 mV, the small, non-inactivated, outward K+ current was TEA sensitive, with an IC50 of 1.5 mM. E, representative traces for currents in response to a voltage step to +10 mV in control solution (Cd2+-free) and in the presence of 400 µM Cd2+. The subtracted record (black trace) shows that the fast, transient A current (*) was almost eliminated while the slowly inactivating current was only modestly affected by Cd2+. F, plot of conductance (G) at 200 ms versus the voltage step indicates that the voltage dependence of activation was little affected by Cd2+ (grey trace; protocol as in Fig. 5C).

Intracellular diffusion of Kv2.1 antibodies inhibited a slowly inactivating K⁺ current

To test whether Kv2.1 subunits underlie the slowly inactivating current, we recorded outward currents under four intracellular conditions: control (without Kv2.1 antibody in the pipette: P21–P30), intracellular anti-Kv2.1 (diluted 1 : 100 for a final concentration of 10 µg ml^–1: P21–P32), neutralized anti-Kv2.1 (1 : 1 antibody to antigen, see Methods: P15–P27), and anti-Kv2.2 (10 µg ml^–1: P21–P33). In most cases, we used the rabbit polyclonal antibody (Alamone: n = 8 cells: P21–P32), which blocked 38 ± 7% at 8 min. Similar results were obtained with the monoclonal antibody (30 ± 6%: n = 3; P27–P28; Neuromab, Upstate) to the C-terminus. Currents were recorded every 10–30 s using the voltage protocol shown in the lower part of Fig. 4B. Currents were normalized to the amplitude of the initial sweep. The average current in the control (n = 9 cells) and the neutralized-antibody groups (n = 7) changed little over 8 min. In 6 of 16 of these cells, run-up of current (< 20%) was observed in the initial 3–7 min, followed by current run-down. In our previous paper (Guan et al. 2006), we reported that after an initial stable period, average run-down rate was 87 ± 21 pA min^–1 (n = 18). It is notable that the run-down current in that study and in the present study activated much more slowly than the AB-sensitive current (e.g. Fig. 4D: initial current – current at 8 min). These data suggest that a different, slower current dominates run-down.

View larger version (37K): [in this window] [in a new window]   Figure 4.  Including anti-Kv2.1 in the pipette inhibited a slowly activating K+ current A, currents were elicited by a voltage step to –10 mV from a holding potential of –70 mV. These steps were repeated every 10 s. The average current in the control (filled circles) and neutralized antibody (grey triangles) groups changed little over 8 min of recording (4% change). The decline in current was more rapid at times later than 8 min. In contrast, for the group with anti-Kv2.1 in the pipette, the initial decline was much steeper and the current was reduced by an average of 33% at 8 min (significantly different from control). B, a typical example of the effects of intracellular anti-Kv2.1 on the outward K+ currents. During 6 min of intracellular diffusion, anti-Kv2.1 inhibited a persistent current (grey trace). The remaining current activated much more slowly than the anti-Kv2.1-sensitive current. C, histograms (mean ± S.E.M.) for four groups of pyramidal cells: control (without anti-Kv2.1: n = 9), anti-Kv2.1 neutralized by Kv2.1 antigen (n = 7), anti-Kv2.2 in the pipette (n = 4 cells), and anti-Kv2.1 in the pipette. Eight cells were recorded with the polyclonal anti-Kv2.1 and three cells with the monoclonal antibody. At 8 min, 38% of the outward K+ current was reduced in the group with polyclonal anti-Kv2.1 and 30% with the monoclonal anti-Kv2.1 (combined: 33%). In the group with neutralized anti-Kv2.1 or with anti-Kv2.2, current reduction was only 8%. The control current declined by 4%. *Significant difference from control value (P < 0.05: ANOVA, Tukey's multiple comparison test). D, representative traces from a cell recorded with the control internal. Note the much slower activation of the subtracted, run-down current compared with anti-Kv2.1-sensitive current in B.

When Kv2.2 antibody was included in the pipette (10 µg ml^–1), the amplitude of outward K⁺ current declined by 7 ± 9% in 8 min (n = 4), similar to the results with neutralized anti-Kv2.1. These data suggest little Kv2.2 current in soma/proximal dendrites of these truncated, dissociated cells, consistent with our data for Kv2.2 distribution (Fig. 2).

Steady-state activation of anti-Kv2.1-sensitive currents

We studied activation properties of the antibody-sensitive current in four cells with anti-Kv2.1 in the pipette (10 µg ml^–1). We obtained data from a family of voltage steps to various potentials (Fig. 5). Figure 5A and B illustrate current recordings in one pyramidal cell (age: P20) at 0 and 6 min. As seen in Fig. 5A, initial currents were composed of an A-like, rapidly inactivating component and a slowly inactivating component. Under our recording conditions, transient A-type currents were observed in 80% of neurons from animals < P20 (8/10) and 22% from animals P27 (8/36). These data suggest developmental down-regulation of I_A, but the data are skewed by the presence of Cd²⁺, which shifts the activation range for A currents to much more positive voltages (Davidson et al. 1995; Song et al. 1998). In cells with detectable A current, the slowly activating current was prominently inhibited by the Kv2.1 antibody, while the A current was unaffected (Fig. 5B). Figure 5C illustrates antibody-sensitive currents obtained by subtraction of the traces in Fig. 5B from those in Fig. 5A.

View larger version (29K): [in this window] [in a new window]   Figure 5.  Voltage-dependent activation of the anti-Kv2.1-sensitive current Outward K+ currents were activated by series of depolarizing voltages in 10 mV increments from a holding potential of –70 mV (A–D) or –90 mV (E–H). A, example of currents recorded from one pyramidal cell just after break in to whole-cell mode (P20). Note the small fast, transient current (A-type: arrow). B, currents recorded at 6 min from the same cell. Because the slowly activating current was reduced, the A-type current was more obvious (arrow). C, subtraction of records in B from those in A reveals the antibody-sensitive current (inset: voltage protocol). D, steady-state activation curves for the non-A-type current components were obtained by fitting peak current amplitudes to the Boltzmann equation. The antibody (AB)-sensitive currents (), obtained by subtracting the currents at 6–9 min from the currents at 0 min, had a half-activation potential of +3.8 mV with a slope of 13.4 mV. The remaining current () activated at more negative potentials than the AB-sensitive current (half-activation at –3 mV, slope = 14.2 mV). E, representative traces for currents just after break-in from another cell (P28). In this cell, currents were elicited by steps to various potentials after a prepulse to –90 mV for 3 s (to remove inactivation, see inset in G). F, currents in the same cell after 6 min diffusion of polyclonal anti-Kv2.1. G, subtracted records (E – F) to indicate the AB-sensitive current (inset: voltage protocol). H, steady-state activation curve for averaged data from 3 cells using the protocol in G. The anti-Kv2.1-sensitive current had a V1/2 of +0.1 mV (slope, 13.2 mV). The remaining current activated at more negative potentials (V1/2, = –17 mV; slope, 15.7 mV).

(2)

where G_max is the maximum conductance, V_1/2 is the half-activation voltage and V_c is the slope. All three of these parameters were determined by the fit (we did not assume G_max). The steady-state voltage dependence for the anti-Kv2.1-sensitive current was well fitted by a single Boltzmann function, with half-activation (V_1/2) at +3.8 ± 1.1 mV and slope 13.4 ± 0.7 mV. This was very similar to the whole current (V_1/2 0.5 ± 0.9 mV, slope 14 ± 0.7 mV) and more depolarized than the remaining current (V_1/2 –3 ± 0.8 mV, slope 14.2 ± 0.7 mV).

At –70 mV, a substantial fraction of the Kv2.1-mediated current was inactivated (see below). To determine whether the above data were biased to a subset of anti-Kv2.1-sensitive channels, we tested three cells (all P28) following a pre-pulse to –90 mV for 3 s to remove inactivation (Fig. 5E–H). The currents appear similar in form to those obtained from –70 mV and the activation voltage dependence of the anti-Kv2.1-sensitive current was very similar (compare Fig. 5H and 5D: after prepulses: V_1/2 0.1 ± 1.7 mV, slope 13.2 ± 1.5 mV).

Expression and properties of Stromatoxin-sensitive currents in the pyramidal cells

The Kv2.1 antibody sensitivity demonstates that Kv2.1 subunits are major contributors to the slowly inactivating current. It is likely that our data at 8 min diffusion time underestimate the contributions of Kv2.1 due to limits of accessibility of the antibody to the channels and complications due to due current run-down at later recording times (cf. Fig. 4). We therefore sought a complementary way to isolate Kv2 currents. rStromatoxin (ScTx) has been shown to be a potent blocker of both Kv2.1 and Kv2.2 (K_d 30 nM in Xenopus oocytes: Escoubas et al. 2002). ScTX acts as a gating modifier, shifting activation to depolarized potentials. It also effectively blocks Kv4.2, a K⁺ channel subunit responsible for one type of A current (Escoubas et al. 2002). We tested the effects of ScTx on K⁺ currents in pyramidal neurons. -DTX and MTX were always used in the external solutions to exclude contributions of Kv1 channels to the recorded K⁺ current.

To test for ScTx-sensitive currents, a 1 s test step to –10 mV from a holding potential of –70 mV was repeated every 10 s (Fig. 6D). ScTx (250–600 nM) caused a large, rapid and fully reversible reduction in the current for all tested pyramidal neurons (P15–P34: Fig. 6A). The block and wash out of persistent currents (measured at 200 ms) were each well fitted by a single exponential function. The time constants were 19 ± 3.8 s (n = 16) and 33 ± 5.8 s (n = 12) for onset of block and wash out, respectively (Fig. 6B). Under our recording conditions (100 µm Cd²⁺), we noticed a developmental difference in our ability to detect a measurable A current in pyramidal cells. About 80% of cells at P20 or younger had measurable A current (8 of 10), compared with 22% of cells after P28 (8 of 36). The A current appears to be down regulated with age; however, the presence of Cd²⁺ effectively blocks A current in many cells, so we did not study this in detail. In some cells (mostly from animals < P20), both the whole current (-DTX and MTX remaining) and the ScTx-sensitive current contained a small, fast activating, A-like component whose peak was at about 4 ms after step onset (Fig. 6C). This is consistent with ScTX block of Kv4 as well as Kv2 current. In pyramidal cells from other rats (mostly aged 4–5 weeks), the A-like component was not evident (Fig. 6D). At all ages, modest inactivation was observed in the ScTx-sensitive currents during a 1 s step.

View larger version (28K): [in this window] [in a new window]   Figure 6.  rStromatoxin (ScTx), a K+ channel blocker specific for Kv2 and Kv4 subunits, inhibited slowly inactivating K+ current The voltage protocol used to obtain A–F is shown an inset in D. A, the effects of ScTx on K+ current are reversible, allowing repetitive tests on the same cell. B, scatter plots for the time constants () for block of current and subsequent reversal (wash). For doses between 250 and 600 nM, the inhibition of outward current by ScTx can be described by an exponential function of time with a mean time constant of 19 ± 4 s. Reversal of the effects of ScTx occurred with a time constant of 33 ± 6 s. C, in pyramidal neurons from some rats (especially < 3 weeks: see text), a fast, A-like component was evident in the outward current (‘A’ and inset). In these cells, ScTx blocked both the transient component and a portion of the slowly inactivating current. D, for most mature pyramidal neurons (> 4 weeks: see text), this transient component was not prominent and no transient component is evident in the ScTx-sensitive current. Inset: voltage protocol. E, dose–response curve for ScTx. The relative block of the outward K+ current by ScTx increases continuously with ScTx concentration. The effects by ScTx can be well fitted with a single Langmuir isotherm with an IC50 of 186 nM. The data are plotted as mean ± S.E.M. F, the scatter plots show that percentage block of the outward K+ current by ScTx was variable. Block by 500–600 nM ScTx varied from 41% to 79%, with a mean of 58 ± 2%. The mean values are indicated by horizontal lines.

The dose–response relationship for the block by ScTx was tested in three cells (Fig. 6E). An IC₅₀ of 186 nM was obtained using the same fitting equation as for Fig. 3B and D. Two doses of ScTx higher than the IC₅₀ were tested in a large sample of the layer II/III pyramidal neurons (18 at 250–350 nM and 23 at 500–600 nM). The percentage block by 250–350 nM ScTx spanned 27% to 59% (39.9 ± 2.3%; Fig. 6F, Table 1). For 500–600 nM ScTx, the percentage block covered a wide range between 40% and 80% (57.7 ± 2.1%; Fig. 6F, Table 1). These data indicate that most of the slowly activating K⁺ current in the pyramidal neurons was sensitive to ScTx. The wide range of percentage block suggests diversity of expression of the ScTx-sensitive current. There were no differences in percentage block by age of animal (data not shown).

To test whether intracellular anti-Kv2.1 and ScTx block the same current component, we compared block by ScTx before and after action of 10 µg ml^–1 anti-Kv2.1. Whole cell recordings were obtained with internal solution containing anti-Kv2.1. Immediately after breaking into the cell, we recorded current amplitude and then tested block by 300 nM ScTx (Fig. 7). In five cells tested, the initial application of ScTx blocked 1122 ± 228 pA of current (50.8 ± 2.5%; Fig. 7A and D). We then allowed time for the Kv2.1 antibody to block channels. When we retested the response of the cells to ScTx after 8 and 12 min perfusion, the block by ScTx was greatly reduced to 510 ± 272 pA (34.4 ± 6.4%), indicating occlusion of the ScTx effect by anti-Kv2.1 (Fig. 7A and D). In these same five cells, anti-Kv2.1 blocked 789 ± 164 pA after 10–15 min (39 ± 14%). As a control, we tested a second application of ScTx after 8–12 min in three control cells. In these cells, the second application blocked as much current as the first application (Fig. 7D). For the cell in Fig. 7, we plotted the current sensitive to the first application of ScTx and the anti-Kv2.1-sensitive current (obtained by subtracting the current remaining at 15 min perfusion time from the initial current after break into whole-cell mode). The kinetics of the currents obtained by these two means were nearly identical (Fig. 7C). Collectively, these data suggest that anti-Kv2.1 and ScTx block the same current component. A further test is provided by comparison of the biophysical properties of anti-Kv2.1 and SCTx-sensitive currents (see below).

View larger version (30K): [in this window] [in a new window]   Figure 7.  Intracellular anti-Kv2.1 and ScTx both block the same Kv2.1-mediated current Currents were elicited by a 200 ms step to –10 mV from a holding potential of –70 mV (repeated every 10–30 s). Data were obtained from 5 cells with anti-Kv2.1 in the internal solution and three control cells without antibody. A, representative traces for a single cell for current just after break in to whole-cell mode, an initial application of 300 nM ScTx (2 min after break in) and subsequent wash out of ScTx (5 min after break in). Note the large block of current by ScTx and partial recovery. Recovery was not complete because continued perfusion of anti-Kv2.1 blocked current. B, traces from the same cell after 15 min of perfusion of anti-Kv2.1 and re-application of 300 nM ScTx. ScTx blocked less current after 15 min perfusion of anti-Kv2.1. C, subtracted records show the current blocked by the first application of ScTx (ScTx-sensitive) and current blocked by 15 min perfusion of anti-Kv2.1. The kinetics of the currents are strikingly similar, except that ScTx also blocked a fast transient current (*a small amount of transient current is also evident in the anti-Kv2.1 trace, probably due to run-down). D, summary data for ScTx effects in 3 control cells and 5 cells tested with anti-Kv2.1. Left, repeated application of 300 nM () or 600 nM ScTx () in control cells (no antibody) revealed little change in current blocked (left). Middle, in contrast, the amount of current blocked by ScTx was greatly reduced by perfusion with anti-Kv2.1 (at 8–12 min). Data from individual cells are indicated by the same symbol and a line between the points. Right, amount of current blocked by anti-Kv2.1 perfusion. There was a strong correlation between the amount of current blocked by anti-Kv2.1 perfusion and the amplitude of the decrease in ScTx block with time (Pearson r = 0.9874). The effects of ScTx and anti-Kv2.1 for the same cells are indicated by the same symbols.

Previous studies in expression systems showed that inhibition of Kv2 currents by ScTx was voltage dependent, with reversal of apparent block at depolarized voltages (Escoubas et al. 2002). We examined this effect on the ScTx-sensitive currents in pyramidal neurons. Seven pyramidal neurons (P28–P30) were tested with a series of 200 ms voltage steps from a holding potential of –70 mV to various potentials in the control solution (containing -DTX and MTX) and after 600 nM ScTx (Fig. 8). A typical result for a cell without an A-type component is shown in Fig. 8A–C. ScTx (600 nM)-sensitive currents (Fig. 8C) activated more rapidly than the ScTx-insensitive currents (Fig. 8B). At more positive voltages (e.g. +30 mV trace), there was increased apparent inactivation of ScTx-sensitive currents. We hypothesized that this was due to voltage- and time-dependent reversal of the ScTx effect (cf. Escoubas et al. 2002).

View larger version (33K): [in this window] [in a new window]   Figure 8.  Voltage-dependent inhibition by ScTx and activation of ScTx-sensitive current Currents were elicited by a series of voltage steps from –60 mV to +30 mV, repeated at 10 s intervals. The holding potential was –70 mV. A, a typical example of currents recorded in the control solution (P28). B, currents recorded from the same cell after application of 600 nM ScTx. The ScTx-insensitive currents activate more slowly than the ScTx-sensitive current. C, ScTx-sensitive current was obtained by subtraction of traces in B from those in A. Note the similarity in kinetics to the anti-Kv2.1-sensitive current in Fig. 4B. One exception is that the ScTx-sensitive current elicited by the step to +30 mV showed a rapid decline in amplitude during the step. This finding is consistent with known, voltage-dependent effects of ScTx. D, voltage protocol for A–C. E, voltage dependence of ScTx effects. Percentage block at 20 ms and 200 ms for voltage steps to several potentials. At potentials depolarized to –10 mV, the percentage block at 20 ms is reduced. This is more dramatic at 200 ms into the step than at 20 ms, reflecting the kinetics of the voltage-dependent reversal of the ScTx effect. F, steady-state activation curve for the slowly activating, ScTx-sensitive currents. Peak G is plotted for averaged data from 4 cells without a detectable A current (mean ± S.E.M.). The half-activation potential for the ScTx-sensitive current was –3 mV (slope, 10.5 mV).

Voltage dependence of steady-state activation

In four cells where no A-like component was seen (P28–P30), conductance was calculated from peak currents and fitted with the Boltzmann equation (see above). The half-activation potential of the ScTx-sensitive current was –3.1 ± 0.8 mV and the slope was 10.5 ± 0.6 mV (n = 4: Fig. 8F). This value is probably biased in the hyperpolarized direction, due to reversal of ScTX block at depolarized potentials. The whole current had a half-activation voltage of 1.7 ± 1 mV and slope 12.2 ± 0.6 mV.

Reversal potential

To further determine the specific properties of slowly activating ScTx-sensitive currents, tail currents were recorded with and without 600 nM ScTX (Fig. 9). Voltage was stepped to –10 mV for 200 ms from a holding potential of –70 mV, then stepped down to different potentials (–110 to –40 mV). Six cells (P20–38) were recorded from that did not show prominent A currents. Figure 9A shows recordings of the ScTx-sensitive current from a typical pyramidal neuron (P20). Tails of ScTx-sensitive currents demonstrated a reversal potential at –91.8 ± 2.4 mV (Fig. 9B), which agrees well with the calculated E_k (–96.8 mV for internal K⁺ of 140 mM and external K⁺ of 3 mM: determined by the Nernst equation). Two cells were also tested in high K⁺ (50 mM) solution. Again, the tested reversal potential for the ScTx-sensitive currents approximated the calculated E_k (–27.0 mV versus –25.9 mV: Fig. 9B). The tails of the ScTx-insensitive current reversed polarity at –83.5 ± 2.0 mV in 3 mM extracellular K⁺ and also showed a Nernstian shift with raised extracellular K⁺ (Fig. 9B). These data indicated that the channels that underlie the ScTx-sensitive and -insensitive currents are very K⁺ selective.

View larger version (32K): [in this window] [in a new window]   Figure 9.  Reversal potenial and activation and deactivation kinetics of the K+ currents sensitive to polyclonal anti-Kv2.1 or ScTx (600 nM) Time constants were obtained by fitting currents with a single exponential function. A, an example of tail currents sensitive to 600 nM ScTx (P20). The tail currents were elicited by a series of different voltages stepped down from a 200 ms activating potential step of –10 mV (inset). B, both the ScTx-sensitive and –insensitive current components reversed polarity near EK (3 mM K+). The reversal potential also shifted in a Nernstian manner with elevated extracellular K+ (50 mM K+). These data indicate that the channels underlying the ScTx-sensitive and –insensitive currents are very potassium selective. C, activation and deactivation time constants for the ScTx-sensitive and ScTx-insensitive currents. ScTx-sensitive and –insensitive currents have similar kinetics at negative potentials, with the ScTx-insensitive currents being slower at potentials depolarized to –20 mV. D, the activation and deactivation time constants of the ScTx-sensitive and the anti-Kv2.1-sensitive currents were very similar over the entire voltage range tested.

To characterize the kinetics of the slowly inactivating component, currents were recorded at a step potential of –10 mV from a holding potential of –70 mV. The activation time constant was obtained by fitting the currents to the following equation:

(3)

where I is current, I_o is the initial current, t is time, is the time constant, and m is the activation coefficient. The best m value was between 1 and 1.3. For comparisons, m was set to be 1 for all currents. We only used cells with no visible A current and we fitted data from 0 to 200 ms. We used a single first order exponential function to fit the deactivation tails.

Activation and deactivation time constants for the slowly activating components in both ScTx-sensitive and ScTx-insensitive currents are shown in Fig. 9C. Eighteen pyramidal neurons were tested in ScTx (P20–P38: 250–600 nM). The activation time constants of the ScTx-sensitive currents showed no dependence on the concentration of ScTx (data not shown), indicating the high specificity of ScTx to the targeted channels. The mean activation time constant for ScTx-sensitive current at –10 mV was 69 ± 42 ms (Table 1).

The ScTx-sensitive component was faster than the remaining component for voltages above –30 mV. We also tested the activation time constants for the anti-Kv2.1-sensitive current (n = 4 cells). They were very similar over the whole voltage range to those obtained for the ScTx-sensitive component (e.g. 74 ± 25 ms at –10 mV; Table 1, Fig. 9D), consistent with the same channels being targeted by both anti-Kv2.1 and ScTx.

Inactivation and recovery

Inactivation kinetics of the 600 nM ScTx-sensitive component were examined in 15 cells (P17–30). Voltage was held at –70 mV and stepped to –10 mV for 1–3 s. Figure 10A shows a typical example for currents in control solution as well as the currents sensitive and insensitive to 600 nM ScTx. In 11 of 15 cells, the ScTx-sensitive currents reached a peak between 140 ms and 380 ms after the step (Fig. 10A) and then the currents slowly decayed. The inactivation process was well fitted by an exponential function, with time constants between 2.0 s to 25.5 s (7.8 ± 2.1 s: Fig. 10B). The other four cells and all currents remaining after ScTx did not inactivate over 3 s. We obtained 1 s steps to –10 mV for the anti-Kv2.1-sensitive current in six cells (all P32). One cell did not inactivate over 1 s. For the other five cells, the inactivation time constant was 5.2 ± 1.5 s.

View larger version (38K): [in this window] [in a new window]   Figure 10.  Inactivation of ScTx-sensitive currents A, current traces elicited by 1–3 s voltage steps to –10 mV from a holding potential of –70 mV (protocol below traces). Shown are a control trace and currents sensitive and insensitive to 600 nM ScTx (note difference in kinetics between ScTx-sensitive and -insensitive currents) (P30). B, box plot summarizing the time constant () for inactivation determined by fitting the current decline (at –10 mV) with an exponential function. The inactivation time constants for the ScTx-sensitive current were between 2 and 26 s, with a median at 5.2 s (n = 11 cells). For the AB-sensitive current, median was 4.5 s (n = 5 cells). C, holding potential sensitivity of ScTx-sensitive and -insensitive currents. Currents were elicited by a step from –70 to –10 mV (200 ms; not shown). The stimulus was repeated at 10 s intervals. Holding potential was then changed to –40 mV. The plots show the amplitude of currents elicited by the test stimulus as a function of time after the holding potential change. The peak amplitude of the ScTx-sensitive currents decreased with time at –40 mV. The changes were well fitted by an exponential function, with a time constant of 2.5 ± 0.3 s. The ScTx-sensitive currents elicited from the –40 mV holding potential were much smaller than the currents recorded from –80 mV holding potential. This strong holding potential dependence of the ScTx-sensitive current is similar to the TEA-sensitive currents (Fig. 3). D, representative traces for steady-state inactivation of ScTx-sensitive current after 5 s inactivation at various potentials from –100 mV to –20 mV (P30). Voltage protocol is shown as inset below. A series of 5 s inactivation voltage steps of varied potentials were delivered from a holding potential of –70 mV every 15 s and closely followed by a 400 ms test voltage step to –10 mV. E, steady-state inactivation curves were obtained by fitting the averaged recordings from 10 cells with the Boltzmann equation. The ScTx-sensitive currents () had a half-inactivation potential of –60 mV (slope, 12.5 mV). Average data from 6 cells where steady-state inactivation was tested for the polyclonal anti-Kv2.1-sensitive current are illustrated by open squares (P30; V1/2 = – 62 mV, slope = 11.5 mV). The data are very similar to the ScTx-sensitive currents. Most of the ScTx-insensitive current () did not inactivate with this protocol. The half-inactivation potential for the ScTx-insensitive component that did inactivate was –87 mV. F, scatter plots summarizing the half-inactivation and slope data for ScTx-sensitive and anti-Kv2.1 (AB)-sensitive current. The data are very similar for the two ways of isolating Kv2.1 currents.

The steady-state voltage dependence of inactivation of the ScTx-sensitive current was studied in seven cells (P28–P30). Voltage was held at –70 mV and stepped to various inactivation potentials for 5 s. These prepulses were followed by a 400 ms test pulse to –10 mV. Figure 10D shows a typical example of the 600 nM ScTx-sensitive currents after 5 s inactivation at various potentials. Peak currents were measured during the –10 mV test pulse and were fitted by the Boltzmann equation of the form:

(4)

(Fig. 10E). The ScTx-sensitive currents had a half-inactivation potential of –60.1 ± 1.6 mV and the slope was 12.5 ± 0.2 mV (Fig. 10E and F). About 30% of the ScTx-insensitive current inactivated, with a half-inactivation potential of –83.6 ± 2.5 mV (slope 11.0 ± 1.6 mV: Fig. 10E). The whole current had a half-inactivation potential of –62 ± 2.0 mV and the slope was 14 ± 0.5 mV (P < 0.001; n = 7).

In six cells, steady-state inactivation was obtained for the current blocked by intracellular anti-Kv2.1. The half-inactivation voltages (–62 ± 3.0 mV) and slopes (11.5 ± 1.1 mV) for these cells were very similar to values obtained with ScTx (Table 1; Fig. 10E and F).

Recovery from inactivation for ScTx-sensitive current was tested in eight cells (P28–30) using the voltage protocol shown in the lower portion of Fig. 11A. Currents were first inactivated by holding at –48 mV for at least 12 s. Then, a 200 ms test pulse to –10 mV was delivered and followed by a recovery pulse at –100 mV of various durations. At the end of the recovery pulses, the test pulse was delivered again. Figure 11A shows typical ScTx-sensitive currents. Most ScTx-sensitive currents had been inactivated at –48 mV. Their recovery process at –100 mV could be well characterized by a single exponential function of time with a time constant of 918 ± 67 ms (n = 8). The remaining currents had two components, one was not inactivated at –48 mV, and one that recovered with a time constant of 170 ± 7 ms (n = 8). We tested recovery from inactivation in nine cells (P28–P32) recorded in the presence of the polyclonal anti-Kv2.1 antibody. At –100 mV, the recovery time constant was not significantly different from the ScTx-sensitive current in these cells (793 ± 123 ms: data not shown).

View larger version (19K): [in this window] [in a new window]   Figure 11.  Recovery from inactivation of the ScTx-sensitive currents was tested in 5 cells using a protocol shown in the lower part of A The currents were inactivated at a holding potential of –48 mV. A 200 ms test pulse of –10 mV was delivered and followed by a recovery voltage step of –100 mV. The duration of the recovery voltage step varied from 0.02 to 1.77 s with increments of 0.25 s. A second test pulse of –10 mV was delivered after the recovery voltage step. Currents in response to the second test pulse were analysed relative to the first test step. A, typical example of the recovered ScTx-sensitive currents (P30). B, the peak recovered ScTx-sensitive currents can be well fitted by an exponential function, yielding a recovery time constant of 920 ms. Similar data were obtained for the AB-sensitive current (see text). The recovery time constant for the ScTx-insensitive component was 170 ms.

	Discussion

Top Abstract Introduction Methods Results Discussion References

We report here that Kv2.1 subunits are the major contributor to the slowly inactivating K⁺ current in neocortical pyramidal neurons. We found expression of both Kv2.1 and Kv2.2 mRNAs and proteins in pyramidal cells, with a pronounced difference in the localization of the two subunits. Whereas Kv2.1 subunits were expressed by virtually all pyramidal cells in the soma and proximal apical dendrite, Kv2.2 subunit protein was primarily expressed throughout the apical dendrites of a subset of pyramidal cells from deep layers (V/VI). We identified Kv2-mediated currents with intracellular application of a Kv2.1 antibody and compared the anti-Kv2.1-sensitive currents with current sensitive to the gating modifier rStromatoxin-1 (ScTx). A striking finding was that the Kv2.1 current was very holding potential sensitive.

Our finding of current blocked by anti-Kv2.1 (but not neutralized anti-Kv2.1 or anti-Kv2.2) is strong evidence for involvement of Kv2.1 subunits underlying the slowly inactivating current. Most of our experiments employed the polyclonal anti-Kv2.1 (Trimmer, 1991) previously shown to block Kv2.1 currents in cultured hippocampal pyramidal neurons (Murakoshi & Trimmer, 1999) and smooth muscle (Archer et al. 1998; Lu et al. 2002). We obtained similar results with a monoclonal antibody to the C-terminus of Kv2.1 (NeuroMab).

Expression of Kv2.1 and Kv2.2 subunits

Kv2.1 subunits are widely expressed in the mammalian brain (Frech et al. 1989; Hwang et al. 1993; Du et al. 1998; Trimmer & Rhodes, 2004; Misonou et al. 2005). In hippocampal and layer V neocortical pyramidal cells (Hwang et al. 1993; Du et al. 1998; Antonucci et al. 2001) and in spinal motoneurons (Muennich & Fyffe, 2004), Kv2.1 subunits are localized to variably sized clusters on soma and proximal dendrites. These subunits are not found in axons. The clustering is dependent upon phosphorylation state; dephosphorylation causes dispersion of the clusters (Misonou et al. 2004). In the present study, we confirmed this localization of Kv2.1 subunits to clusters in soma and proximal dendrites of pyramidal cells. Virtually all pyramidal cells expressed Kv2.1 mRNA and protein.

Kv2.2 subunits are not as widely expressed as Kv2.1. In cortex, they have been reported to primarily localize to interneurons (Hwang et al. 1993). We found that a large percentage of pyramidal cells in all layers also expressed Kv2.2 mRNA. We also found striking differences in the expression of Kv2.1 versus Kv2.2 protein in neocortical pyramidal neurons. In contrast to the soma/proximal dendritic expression of Kv2.1 in all pyramidal cells, Kv2.2 subunits were not clustered in the manner of Kv2.1 subunits and were primarily localized to apical dendrites of a subset of deep (layers V/VI) pyramidal cells. These differences in distribution are consistent with the idea that Kv2.1 and Kv2.2 subunits are not combined in heteromultimeric channels in situ (Blaine & Ribera, 1998, 2001; Lim et al. 2000).

The ultrastructural findings for Kv2.2 were intriguing in that the bulk of the staining looked vesicular and these vesicles were distributed throughout the dendrites, suggestive of transport of the vesicles through the apical dendrites. Perhaps despite limited expression in the plasma membrane, these subunits are subject to rapid turnover.

Kv2.1 subunits contribute to slowly inactivating current

Due to their nearly ubiquitous distribution, Kv2.1 subunits are often assumed to underlie the dominant delayed rectifier current, although this has only been shown in a small number of neuron types. Murakoshi & Trimmer (1999) used intracellular application of a polyclonal antibody to the C-terminus of the Kv2.1 subunit to identify Kv2.1 as the major contributor to the delayed rectifier current in cultur