|
|
||||||||
AJP - Cell Physiology, Vol 257, Issue 1 C77-C85, Copyright © 1989 by American Physiological Society
ARTICLES |
E. K. Gallin
Department of Physiology, Armed Forces Radiobiology Research Institute, Bethesda, Maryland 20854.
Cell-attached patch studies of cultured human macrophages demonstrate that exposure to ionomycin induces inward-rectifying single-channel currents that differ from the voltage-dependent 28 pS inward-rectifying K currents previously described in these cells (J. Membr. Biol. 103: 55-66, 1988). With 150 mM KCl in the electrode and NaCl Hanks' solution in the bath, the ionomycin-induced single-channel conductance for inward currents was 37 pS, and the reversal potential was 57 mV. Channel activity was often associated with a shift in the base-line current level indicating that the cell membrane potential hyperpolarized. The ability of ionomycin to induce channel activity depended on extracellular [Ca] supporting the view that the channels were gated by calcium. Ionomycin-induced channels were permeable to K, relatively impermeable to Cl or Na, exhibited bursting kinetics, and had no apparent voltage dependence. Barium (3 mM in the patch electrode) did not significantly block the ionomycin-induced channel at rest but blocked channel activity when the patch was hyperpolarized beyond the resting membrane potential. Exposure of macrophages to platelet-activating factor, which is known to increase intracellular [Ca] [( Ca]i) (J. Cell Biol. 103: 439-450, 1986), also transiently induced channel activity. In excised patches with 3 microM [Ca]i bursting inward-rectifying channels with a 41 pS conductance were noted that probably correspond to the ionomycin-induced channels present in cell-attached patches. Increasing [Ca]i from 10(-8) to 3 x 10(-6) M induced inward-rectifying channel activity in previously quiescent excised patches.(ABSTRACT TRUNCATED AT 250 WORDS)
This article has been cited by other articles:
![]() |
A. Schwab Function and spatial distribution of ion channels and transporters in cell migration Am J Physiol Renal Physiol, May 1, 2001; 280(5): F739 - F747. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Sullivan, S. K. Koliwad, and D. L. Kunze Analysis of a Ca2+-activated K+ channel that mediates hyperpolarization via the thrombin receptor pathway Am J Physiol Cell Physiol, November 1, 1998; 275(5): C1342 - C1348. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Eder Ion channels in microglia (brain macrophages) Am J Physiol Cell Physiol, August 1, 1998; 275(2): C327 - C342. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. J. Logsdon, J. Kang, J. A. Togo, E. P. Christian, and J. Aiyar A Novel Gene, hKCa4, Encodes the Calcium-activated Potassium Channel in Human T Lymphocytes J. Biol. Chem., December 26, 1997; 272(52): 32723 - 32726. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |