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STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids

Fixation of (131)I-serum albumin by Ehrlich ascites tumor cells in suspensions and sarcoma S-180 monolayers was measured under experimental conditions. Anaerobic incubation and inhibitors of the oxidative metabolism critically restricted the range of glucose concentrations capable of supporting cell...

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Autor principal: Ryser, Hugues J.-P.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1967
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2107262/
https://www.ncbi.nlm.nih.gov/pubmed/6034487
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author Ryser, Hugues J.-P.
author_facet Ryser, Hugues J.-P.
author_sort Ryser, Hugues J.-P.
collection PubMed
description Fixation of (131)I-serum albumin by Ehrlich ascites tumor cells in suspensions and sarcoma S-180 monolayers was measured under experimental conditions. Anaerobic incubation and inhibitors of the oxidative metabolism critically restricted the range of glucose concentrations capable of supporting cell life; in glucose concentrations higher than 10(-2) M, Ehrlich cells suffered from their own acid production; in concentrations 10(-2) M, lower than they underwent damage by starvation. Both types of damage were accompanied by increased albumin fixation unrelated to pinocytosis. Different procedures recommended to enhance the uptake of infectious viral RNA by animal cells in culture were tested for their ability to increase albumin uptake. They enhanced the penetration of both albumin and vital dyes and decreased the viability of cell populations. Their effect, therefore, is related to cell damage. It was postulated that reversible damage to cells favors RNA infection by leading to abnormal uptake processes and by decreasing intracellular digestion. This abnormal uptake is different from pinocytosis and also from the massive fixation of albumin to dead cells. The latter phenomenon is due to adsorption by intracellular sites exposed by disruption of the cell membrane. Polycations are able to induce all three forms of fixation depending on the experimental conditions.
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spelling pubmed-21072622008-05-01 STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids Ryser, Hugues J.-P. J Cell Biol Article Fixation of (131)I-serum albumin by Ehrlich ascites tumor cells in suspensions and sarcoma S-180 monolayers was measured under experimental conditions. Anaerobic incubation and inhibitors of the oxidative metabolism critically restricted the range of glucose concentrations capable of supporting cell life; in glucose concentrations higher than 10(-2) M, Ehrlich cells suffered from their own acid production; in concentrations 10(-2) M, lower than they underwent damage by starvation. Both types of damage were accompanied by increased albumin fixation unrelated to pinocytosis. Different procedures recommended to enhance the uptake of infectious viral RNA by animal cells in culture were tested for their ability to increase albumin uptake. They enhanced the penetration of both albumin and vital dyes and decreased the viability of cell populations. Their effect, therefore, is related to cell damage. It was postulated that reversible damage to cells favors RNA infection by leading to abnormal uptake processes and by decreasing intracellular digestion. This abnormal uptake is different from pinocytosis and also from the massive fixation of albumin to dead cells. The latter phenomenon is due to adsorption by intracellular sites exposed by disruption of the cell membrane. Polycations are able to induce all three forms of fixation depending on the experimental conditions. The Rockefeller University Press 1967-03-01 /pmc/articles/PMC2107262/ /pubmed/6034487 Text en Copyright © 1967 by The Rockefeller University 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
Ryser, Hugues J.-P.
STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title_full STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title_fullStr STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title_full_unstemmed STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title_short STUDIES ON PROTEIN UPTAKE BY ISOLATED TUMOR CELLS : III. Apparent Stimulations due to pH, Hypertonicity, Polycations, or Dehydration and Their Relation to the Enhanced Penetration of Infectious Nucleic Acids
title_sort studies on protein uptake by isolated tumor cells : iii. apparent stimulations due to ph, hypertonicity, polycations, or dehydration and their relation to the enhanced penetration of infectious nucleic acids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2107262/
https://www.ncbi.nlm.nih.gov/pubmed/6034487
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