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Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets
We have examined the ability of macrophages (Mphi) to transmit T-cell derived suppressor signals to other T cells. The suppressor signal studied is an antigen-specific factor which suppresses the ability of adoptively transferred, sensitized lymphocytes to express contact hypersensitivity in normal...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1978
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184951/ https://www.ncbi.nlm.nih.gov/pubmed/308980 |
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collection | PubMed |
description | We have examined the ability of macrophages (Mphi) to transmit T-cell derived suppressor signals to other T cells. The suppressor signal studied is an antigen-specific factor which suppresses the ability of adoptively transferred, sensitized lymphocytes to express contact hypersensitivity in normal recipients. We have found that this factor binds to peritoneal exudate Mphi via cell surface structures which can be blocked with heat-aggregated gamma globulin. Dead (HK) Mphi bind the factor but fail to present it in a functional way to assay (immune) T cells, whereas live (L) Mphi perform both functions. Further, L Mphi can retrieve the factor in an active form from the surfaces of HK Mphi. Based on these and other findings (1-5), we discuss the possibility that Mphi may play as important a role in presenting T-cell communication signals to the cells of the immune system as they do in presenting antigen. |
format | Text |
id | pubmed-2184951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1978 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21849512008-04-17 Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets J Exp Med Articles We have examined the ability of macrophages (Mphi) to transmit T-cell derived suppressor signals to other T cells. The suppressor signal studied is an antigen-specific factor which suppresses the ability of adoptively transferred, sensitized lymphocytes to express contact hypersensitivity in normal recipients. We have found that this factor binds to peritoneal exudate Mphi via cell surface structures which can be blocked with heat-aggregated gamma globulin. Dead (HK) Mphi bind the factor but fail to present it in a functional way to assay (immune) T cells, whereas live (L) Mphi perform both functions. Further, L Mphi can retrieve the factor in an active form from the surfaces of HK Mphi. Based on these and other findings (1-5), we discuss the possibility that Mphi may play as important a role in presenting T-cell communication signals to the cells of the immune system as they do in presenting antigen. The Rockefeller University Press 1978-08-01 /pmc/articles/PMC2184951/ /pubmed/308980 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 Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title | Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title_full | Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title_fullStr | Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title_full_unstemmed | Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title_short | Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets |
title_sort | intermediary role of macrophages in the passage of suppressor signals between t-cell subsets |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184951/ https://www.ncbi.nlm.nih.gov/pubmed/308980 |