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The Active Transport of Sodium by Ghosts of Human Red Blood Cells

The outflux of Na(24) from prelabeled ghosts was measured under various conditions. Prelabeling was accomplished by hypotonic hemolysis of intact human cells in the presence of tracer Na(24). The resultant ghosts when subsequently washed were found to retain 10 to 20 per cent of the initial Na(24)....

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Detalles Bibliográficos
Autor principal: Hoffman, Joseph F.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1962
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195228/
https://www.ncbi.nlm.nih.gov/pubmed/13908117
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author Hoffman, Joseph F.
author_facet Hoffman, Joseph F.
author_sort Hoffman, Joseph F.
collection PubMed
description The outflux of Na(24) from prelabeled ghosts was measured under various conditions. Prelabeling was accomplished by hypotonic hemolysis of intact human cells in the presence of tracer Na(24). The resultant ghosts when subsequently washed were found to retain 10 to 20 per cent of the initial Na(24). Separate experiments indicated that this trapped amount resides in only a portion of ghosts comprising the total population. The characteristics of the outflux of this residual Na(24) indicated that the ghost system closely resembles intact red cells. The outflux of Na from ghosts could be divided into three components: active and passive transport and exchange diffusion. The active transport system, necessarily driven by metabolism, required the presence of K in the extracellular phase and was blocked by strophanthidin. The concentration dependence of the Na pump flux on the external K and internal Na appeared the same in ghosts as in intact cells. Certain other features of this ghost system are also discussed.
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spelling pubmed-21952282008-04-23 The Active Transport of Sodium by Ghosts of Human Red Blood Cells Hoffman, Joseph F. J Gen Physiol Article The outflux of Na(24) from prelabeled ghosts was measured under various conditions. Prelabeling was accomplished by hypotonic hemolysis of intact human cells in the presence of tracer Na(24). The resultant ghosts when subsequently washed were found to retain 10 to 20 per cent of the initial Na(24). Separate experiments indicated that this trapped amount resides in only a portion of ghosts comprising the total population. The characteristics of the outflux of this residual Na(24) indicated that the ghost system closely resembles intact red cells. The outflux of Na from ghosts could be divided into three components: active and passive transport and exchange diffusion. The active transport system, necessarily driven by metabolism, required the presence of K in the extracellular phase and was blocked by strophanthidin. The concentration dependence of the Na pump flux on the external K and internal Na appeared the same in ghosts as in intact cells. Certain other features of this ghost system are also discussed. The Rockefeller University Press 1962-05-01 /pmc/articles/PMC2195228/ /pubmed/13908117 Text en Copyright © Copyright, 1962, by The Rockefeller Institute Press 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 Article
Hoffman, Joseph F.
The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title_full The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title_fullStr The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title_full_unstemmed The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title_short The Active Transport of Sodium by Ghosts of Human Red Blood Cells
title_sort active transport of sodium by ghosts of human red blood cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195228/
https://www.ncbi.nlm.nih.gov/pubmed/13908117
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