Cargando…
Volume-responsive sodium and proton movements in dog red blood cells
Shrinkage of dog red blood cells (RBC) activates a Na transport pathway that is Cl dependent, amiloride sensitive, and capable of conducting Na- proton counterflow. It is possible to establish transmembrane gradients for either Na or protons and to demonstrate that each cation species can drive reci...
Formato: | Texto |
---|---|
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1984
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228747/ https://www.ncbi.nlm.nih.gov/pubmed/6090579 |
_version_ | 1782149965918765056 |
---|---|
collection | PubMed |
description | Shrinkage of dog red blood cells (RBC) activates a Na transport pathway that is Cl dependent, amiloride sensitive, and capable of conducting Na- proton counterflow. It is possible to establish transmembrane gradients for either Na or protons and to demonstrate that each cation species can drive reciprocal movements of the other. The nature of the coupling between Na and proton movements was investigated using the fluorescent probe diS-C3(5) and also by an indirect method in which K movements through valinomycin channels were used to draw inferences about the membrane potential. No evidence was found to suggest that the Na-proton pathway activated by shrinkage of dog RBC is a conductive one. By exclusion, it is presumed that the coupling between the counterflow of Na and protons is electroneutral. The volume-activated Na-proton fluxes in dog RBC have certain properties that distinguish them from similar transport pathways in other cell types. |
format | Text |
id | pubmed-2228747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22287472008-04-23 Volume-responsive sodium and proton movements in dog red blood cells J Gen Physiol Articles Shrinkage of dog red blood cells (RBC) activates a Na transport pathway that is Cl dependent, amiloride sensitive, and capable of conducting Na- proton counterflow. It is possible to establish transmembrane gradients for either Na or protons and to demonstrate that each cation species can drive reciprocal movements of the other. The nature of the coupling between Na and proton movements was investigated using the fluorescent probe diS-C3(5) and also by an indirect method in which K movements through valinomycin channels were used to draw inferences about the membrane potential. No evidence was found to suggest that the Na-proton pathway activated by shrinkage of dog RBC is a conductive one. By exclusion, it is presumed that the coupling between the counterflow of Na and protons is electroneutral. The volume-activated Na-proton fluxes in dog RBC have certain properties that distinguish them from similar transport pathways in other cell types. The Rockefeller University Press 1984-09-01 /pmc/articles/PMC2228747/ /pubmed/6090579 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Volume-responsive sodium and proton movements in dog red blood cells |
title | Volume-responsive sodium and proton movements in dog red blood cells |
title_full | Volume-responsive sodium and proton movements in dog red blood cells |
title_fullStr | Volume-responsive sodium and proton movements in dog red blood cells |
title_full_unstemmed | Volume-responsive sodium and proton movements in dog red blood cells |
title_short | Volume-responsive sodium and proton movements in dog red blood cells |
title_sort | volume-responsive sodium and proton movements in dog red blood cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228747/ https://www.ncbi.nlm.nih.gov/pubmed/6090579 |