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Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells
The effect of epidermal growth factor (EGF) on gastric acid secretion was correlated with the morphological changes of the apical pole of rat parietal cells studied by transmission electron microscopy. Gastric acid secretion was stimulated by histamine, carbachol, pentagastrin, and insulin-induced h...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111733/ https://www.ncbi.nlm.nih.gov/pubmed/7009622 |
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collection | PubMed |
description | The effect of epidermal growth factor (EGF) on gastric acid secretion was correlated with the morphological changes of the apical pole of rat parietal cells studied by transmission electron microscopy. Gastric acid secretion was stimulated by histamine, carbachol, pentagastrin, and insulin-induced hypoglycemia, and estimated by continuous recording of pH variations of gastric luminal perfusate. EGF inhibits acid secretion in these conditions. The action of the hormone also results in the arrest or reversal of the changes in shape undergone by parietal cells as they go into secretion. In view of the evidence involving cytoskeletal elements in the generation of these structural alterations, our observations suggest that the action of EGF on gastric acid secretion may be a consequence of a general effect of this hormone on cytoskeletal function. |
format | Text |
id | pubmed-2111733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21117332008-05-01 Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells J Cell Biol Articles The effect of epidermal growth factor (EGF) on gastric acid secretion was correlated with the morphological changes of the apical pole of rat parietal cells studied by transmission electron microscopy. Gastric acid secretion was stimulated by histamine, carbachol, pentagastrin, and insulin-induced hypoglycemia, and estimated by continuous recording of pH variations of gastric luminal perfusate. EGF inhibits acid secretion in these conditions. The action of the hormone also results in the arrest or reversal of the changes in shape undergone by parietal cells as they go into secretion. In view of the evidence involving cytoskeletal elements in the generation of these structural alterations, our observations suggest that the action of EGF on gastric acid secretion may be a consequence of a general effect of this hormone on cytoskeletal function. The Rockefeller University Press 1981-01-01 /pmc/articles/PMC2111733/ /pubmed/7009622 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 Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title | Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title_full | Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title_fullStr | Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title_full_unstemmed | Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title_short | Epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
title_sort | epidermal growth factor inhibits cytoskeleton-related changes in the surface of parietal cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111733/ https://www.ncbi.nlm.nih.gov/pubmed/7009622 |