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Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages
Receptors for IgG stimulate the release of approximately 20% of cellular arachidonic acid (20:4) from murine resident peritoneal macrophages. In contrast, C3 receptors do not trigger the secretion of any 20:4 in excess of that released constitutively from the cells. Since the ability of C3 receptors...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1985
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187583/ https://www.ncbi.nlm.nih.gov/pubmed/3156206 |
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collection | PubMed |
description | Receptors for IgG stimulate the release of approximately 20% of cellular arachidonic acid (20:4) from murine resident peritoneal macrophages. In contrast, C3 receptors do not trigger the secretion of any 20:4 in excess of that released constitutively from the cells. Since the ability of C3 receptors to promote phagocytosis is regulated, we compared resting macrophages, whose C3 receptors do not promote phagocytosis of C3-coated particles, and lymphokine-treated cells, whose receptors do promote ingestion. Despite their ability to promote phagocytosis, the C3 receptor of lymphokine-treated macrophages remain unable to initiate release of 20:4. We speculate that the intracellular signals that initiate phagocytosis are distinct from those that initiate release of 20:4. |
format | Text |
id | pubmed-2187583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21875832008-04-17 Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages J Exp Med Articles Receptors for IgG stimulate the release of approximately 20% of cellular arachidonic acid (20:4) from murine resident peritoneal macrophages. In contrast, C3 receptors do not trigger the secretion of any 20:4 in excess of that released constitutively from the cells. Since the ability of C3 receptors to promote phagocytosis is regulated, we compared resting macrophages, whose C3 receptors do not promote phagocytosis of C3-coated particles, and lymphokine-treated cells, whose receptors do promote ingestion. Despite their ability to promote phagocytosis, the C3 receptor of lymphokine-treated macrophages remain unable to initiate release of 20:4. We speculate that the intracellular signals that initiate phagocytosis are distinct from those that initiate release of 20:4. The Rockefeller University Press 1985-03-01 /pmc/articles/PMC2187583/ /pubmed/3156206 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 Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title | Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title_full | Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title_fullStr | Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title_full_unstemmed | Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title_short | Ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
title_sort | ligated complement receptors do not activate the arachidonic acid cascade in resident peritoneal macrophages |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187583/ https://www.ncbi.nlm.nih.gov/pubmed/3156206 |