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Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction

Rat lymphocytes in mixed cultures can reutilize tritiated thymidine from labeled granulocytes. Shortly after thymidine injections in vivo, major effects on the frequency of labeled lymphocyte mitoses in peripheral blood cultures are introduced by 10-20% polymorph contamination, even though transfer...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1975
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189875/
https://www.ncbi.nlm.nih.gov/pubmed/125313
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description Rat lymphocytes in mixed cultures can reutilize tritiated thymidine from labeled granulocytes. Shortly after thymidine injections in vivo, major effects on the frequency of labeled lymphocyte mitoses in peripheral blood cultures are introduced by 10-20% polymorph contamination, even though transfer of label via supernates is not demonstrable. Cold thymidine in the cultures prevents reutilization, and has permitted reevaluation of several previous conclusions concerning the life history of lymphocytes reactive to major histocompatibility alloantigens (HARC). Rather than being predominantly recently divided cells, HARC do not appear to have an age distribution, in blood or lymph, significantly different from the general recirculating lymphocyte population. However, the ability of immunization across strong allogeneic differences to increase markedly the proportion of young HARC among the specifically responsive population has been confirmed.
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spelling pubmed-21898752008-04-17 Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction J Exp Med Articles Rat lymphocytes in mixed cultures can reutilize tritiated thymidine from labeled granulocytes. Shortly after thymidine injections in vivo, major effects on the frequency of labeled lymphocyte mitoses in peripheral blood cultures are introduced by 10-20% polymorph contamination, even though transfer of label via supernates is not demonstrable. Cold thymidine in the cultures prevents reutilization, and has permitted reevaluation of several previous conclusions concerning the life history of lymphocytes reactive to major histocompatibility alloantigens (HARC). Rather than being predominantly recently divided cells, HARC do not appear to have an age distribution, in blood or lymph, significantly different from the general recirculating lymphocyte population. However, the ability of immunization across strong allogeneic differences to increase markedly the proportion of young HARC among the specifically responsive population has been confirmed. The Rockefeller University Press 1975-07-01 /pmc/articles/PMC2189875/ /pubmed/125313 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
Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title_full Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title_fullStr Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title_full_unstemmed Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title_short Proliferation in vivo of T lymphocytes reactive to histocompatibility alloantigens: a correction
title_sort proliferation in vivo of t lymphocytes reactive to histocompatibility alloantigens: a correction
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189875/
https://www.ncbi.nlm.nih.gov/pubmed/125313