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HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes

PPD-sensitized monocytes and macrophages from tuberculin-positive subjects are both capable of inducing blastogenic transformation of autologous lymphocytes. Incorporation of thymidine-(3)H and morphological transformation were always greater in lymphocyte cultures containing macrophages than in tho...

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Detalles Bibliográficos
Autores principales: Hanifin, J. M., Cline, M. J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1970
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108075/
https://www.ncbi.nlm.nih.gov/pubmed/5459014
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author Hanifin, J. M.
Cline, M. J.
author_facet Hanifin, J. M.
Cline, M. J.
author_sort Hanifin, J. M.
collection PubMed
description PPD-sensitized monocytes and macrophages from tuberculin-positive subjects are both capable of inducing blastogenic transformation of autologous lymphocytes. Incorporation of thymidine-(3)H and morphological transformation were always greater in lymphocyte cultures containing macrophages than in those containing monocytes. More lymphocytes entered the first detectable S phase in cultures containing macrophages. Lymphocyte DNA synthesis occurred as early as 40 hr of culture and always in cells in contact with mononuclear phagocytes. By 120–144 hr, many transformed lymphocytes were free in suspension; at the same time, the "immunological cluster" had increased greatly in size and contained transformed and untransformed lymphocytes. The greater effectiveness of macrophages at induction of lymphocyte transformation may be related to the efficiency of this cell type at trapping antigen and its effectiveness at making contact with and binding lymphocytes.
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spelling pubmed-21080752008-05-01 HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes Hanifin, J. M. Cline, M. J. J Cell Biol Article PPD-sensitized monocytes and macrophages from tuberculin-positive subjects are both capable of inducing blastogenic transformation of autologous lymphocytes. Incorporation of thymidine-(3)H and morphological transformation were always greater in lymphocyte cultures containing macrophages than in those containing monocytes. More lymphocytes entered the first detectable S phase in cultures containing macrophages. Lymphocyte DNA synthesis occurred as early as 40 hr of culture and always in cells in contact with mononuclear phagocytes. By 120–144 hr, many transformed lymphocytes were free in suspension; at the same time, the "immunological cluster" had increased greatly in size and contained transformed and untransformed lymphocytes. The greater effectiveness of macrophages at induction of lymphocyte transformation may be related to the efficiency of this cell type at trapping antigen and its effectiveness at making contact with and binding lymphocytes. The Rockefeller University Press 1970-07-01 /pmc/articles/PMC2108075/ /pubmed/5459014 Text en Copyright © 1970 by The Rockefeller University Press 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 Article
Hanifin, J. M.
Cline, M. J.
HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title_full HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title_fullStr HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title_full_unstemmed HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title_short HUMAN MONOCYTES AND MACROPHAGES : Interaction with Antigen and Lymphocytes
title_sort human monocytes and macrophages : interaction with antigen and lymphocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108075/
https://www.ncbi.nlm.nih.gov/pubmed/5459014
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