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AJP - Cell Physiology, Vol 272, Issue 4 C1099-C1111, Copyright © 1997 by American Physiological Society
ARTICLES |
M. Berenbrink, Y. R. Weaver and A. R. Cossins
Integrative Physiology Research Group, School of Biological Science, University of Liverpool, United Kingdom.
The volume sensitivity of different K flux pathways has been determined in trout red blood cells subjected to volume perturbation. Gentle hyposmotic swelling induced a K influx in a Cl-containing saline but not in NO3- or methanesulfonate (MeSF)-containing salines, consistent with the activation of a Cl-dependent flux. Extreme hyposmotic swelling led to larger K fluxes in all salines but with reduced anion discrimination of the Cl-dependent flux. In contrast to these graded responses, isosmotic swelling using ammonium chloride or beta-adrenergic stimulation activated only Cl-dependent fluxes in an all-or-none fashion. The relationship between the hyposmotically and isosmotically induced pathways was studied by coactivation using either ammonium chloride or isoproterenol with anisosmotic treatment. Cells in ammonium chloride-containing hyposmotic salines showed no additive K flux over that induced by hyposmotic treatment alone, indicating that the isosmotically induced Cl-dependent flux was identical to the hyposmotically induced Cl-dependent flux. However, cells coactivated by hyposmotic and beta-adrenergic treatment showed a small Cl-dependent flux in addition to that induced by hyposmotic treatment alone. This small third component was unaffected by anisosmotic treatment. We conclude that the major Cl-dependent and Cl-independent K flux pathways are distinct and separate and that the former has an anion dependence that varies with cell volume and a volume sensitivity that varies with ionic strength.
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H. Guizouarn and R. Motais Swelling activation of transport pathways in erythrocytes: effects of Cl-, ionic strength, and volume changes Am J Physiol Cell Physiol, January 1, 1999; 276(1): C210 - C220. [Abstract] [Full Text] [PDF] |
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