A voltage-gated K+ conductance resembling that of the human ether-à-go-go-related gene product (HERG) was studied using whole-cell voltage-clamp recording, and found to be the predominant conductance at hyperpolarized potentials in a cell line (MLS-9) derived from primary cultures of rat microglia. Its behavior differed markedly from the classical inward rectifier K+ currents described previously in microglia, but closely resembled HERG currents in cardiac muscle and neuronal tissue. The HERG-like channels opened rapidly on hyperpolarization from 0 mV, and then decayed slowly into an absorbing closed state. The peak K+ conductance–voltage relation was half maximal at −59 mV with a slope factor of 18.6 mV. Availability, assessed by a hyperpolarizing test pulse from different holding potentials, was more steeply voltage dependent, and the midpoint was more positive (−14 vs. −39 mV) when determined by making the holding potential progressively more positive than more negative. The origin of this hysteresis is explored in a companion paper (Pennefather, P.S., W. Zhou, and T.E. DeCoursey. 1998. J. Gen. Physiol. 111:795–805). The pharmacological profile of the current differed from classical inward rectifier but closely resembled HERG. Block by Cs+ or Ba2+ occurred only at millimolar concentrations, La3+ blocked with Ki = ∼40 μM, and the HERG-selective blocker, E-4031, blocked with Ki = 37 nM. Implications of the presence of HERG-like K+ channels for the ontogeny of microglia are discussed.
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1 June 1998
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June 01 1998
HERG-like K+ Channels in Microglia
Wei Zhou,
Wei Zhou
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
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Francisco S. Cayabyab,
Francisco S. Cayabyab
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
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Peter S. Pennefather,
Peter S. Pennefather
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
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Lyanne C. Schlichter,
Lyanne C. Schlichter
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
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Thomas E. DeCoursey
Thomas E. DeCoursey
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
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Wei Zhou
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
Francisco S. Cayabyab
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
Peter S. Pennefather
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
Lyanne C. Schlichter
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
Thomas E. DeCoursey
From the *Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois 60612; ‡Playfair Neuroscience Unit, Toronto Hospital Research Institute, Toronto, Ontario M5T 2S8, Canada; §Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A1, Canada; and ‖Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 2S2, Canada
Address correspondence to Tom DeCoursey, Department of Molecular Biophysics and Physiology, Rush Presbyterian St. Luke's Medical Center, 1653 West Congress Parkway, Chicago, IL 60612. Fax: 312-942-8711; E-mail: [email protected]
Portions of this work were previously published in abstract form (Zhou, W., F.S. Cayabyab, P.S. Pennefather, L.C. Schlichter and T.E. DeCoursey. 1998. Biophys. J. 74:A109).
Received:
August 05 1997
Accepted:
March 18 1998
Online ISSN: 1540-7748
Print ISSN: 0022-1295
1998
J Gen Physiol (1998) 111 (6): 781–794.
Article history
Received:
August 05 1997
Accepted:
March 18 1998
Citation
Wei Zhou, Francisco S. Cayabyab, Peter S. Pennefather, Lyanne C. Schlichter, Thomas E. DeCoursey; HERG-like K+ Channels in Microglia . J Gen Physiol 1 June 1998; 111 (6): 781–794. doi: https://doi.org/10.1085/jgp.111.6.781
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