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Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes
Receptors for prostaglandin E2 or histamine were measured on subpopulations of human lymphocytes, using the cyclic AMP increase after exposure to prostaglandin or histamine as an indicator for the presence of receptors. The cyclic AMP response to prostaglandin E2 was similar in unfractionated lympho...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1979
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185694/ https://www.ncbi.nlm.nih.gov/pubmed/227981 |
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collection | PubMed |
description | Receptors for prostaglandin E2 or histamine were measured on subpopulations of human lymphocytes, using the cyclic AMP increase after exposure to prostaglandin or histamine as an indicator for the presence of receptors. The cyclic AMP response to prostaglandin E2 was similar in unfractionated lymphocytes and the T-enriched and T-depleted fractions. Within the T-enriched population, T cells bearing a receptor for the Fc portion of IgG (T gamma-cells) had a 27.4-fold rise in cyclic AMP after exposure to prostaglandin E2, whereas the remaining T cells (non-T gamma cells) had a fourfold increase. It would appear that prostaglandin receptors are concentrated on a small subfraction of T gamma cells, comprising approximately 15% of the T-cell population. The cyclic AMP response to histamine was less than twofold in all lymphocyte fractions. |
format | Text |
id | pubmed-2185694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1979 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21856942008-04-17 Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes J Exp Med Articles Receptors for prostaglandin E2 or histamine were measured on subpopulations of human lymphocytes, using the cyclic AMP increase after exposure to prostaglandin or histamine as an indicator for the presence of receptors. The cyclic AMP response to prostaglandin E2 was similar in unfractionated lymphocytes and the T-enriched and T-depleted fractions. Within the T-enriched population, T cells bearing a receptor for the Fc portion of IgG (T gamma-cells) had a 27.4-fold rise in cyclic AMP after exposure to prostaglandin E2, whereas the remaining T cells (non-T gamma cells) had a fourfold increase. It would appear that prostaglandin receptors are concentrated on a small subfraction of T gamma cells, comprising approximately 15% of the T-cell population. The cyclic AMP response to histamine was less than twofold in all lymphocyte fractions. The Rockefeller University Press 1979-11-01 /pmc/articles/PMC2185694/ /pubmed/227981 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 Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title | Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title_full | Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title_fullStr | Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title_full_unstemmed | Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title_short | Cyclic adenosine monophosphate response to prostaglandin E2 on subpopulations of human lymphocytes |
title_sort | cyclic adenosine monophosphate response to prostaglandin e2 on subpopulations of human lymphocytes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185694/ https://www.ncbi.nlm.nih.gov/pubmed/227981 |