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Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells

Bacterial lipopolysaccharides (LPS) stimulate mouse peritoneal macrophages to kill tumor cells in vitro. Lysis is confined to tumor cells where it is nonspecific; both allogeneic and syngeneic cells being susceptible. Stimulation by LPS appears to be due to direct interaction between LPS and macroph...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184936/
https://www.ncbi.nlm.nih.gov/pubmed/568163
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description Bacterial lipopolysaccharides (LPS) stimulate mouse peritoneal macrophages to kill tumor cells in vitro. Lysis is confined to tumor cells where it is nonspecific; both allogeneic and syngeneic cells being susceptible. Stimulation by LPS appears to be due to direct interaction between LPS and macrophages and does not involve participation by lymphocytes. After exposure to LPS, a latent period must elapse before macrophages can lyse tumor cells. The cytolytic mechanism requires contact between target cells and viable effector cells which maintain their lytic capacity for a sustained period and can kill on repeated occasions. The generation of a macrophage cytolytic effect by LPS is critically dependent upon the absolute number of macrophages which must be sufficient to produce confluent monolayers. These findings indicate that LPS stimulation of macrophages in vitro represents a valuable model system for the study of the mechanisms of macrophage stimulation and of the mediation of tumor cell death.
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spelling pubmed-21849362008-04-17 Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells J Exp Med Articles Bacterial lipopolysaccharides (LPS) stimulate mouse peritoneal macrophages to kill tumor cells in vitro. Lysis is confined to tumor cells where it is nonspecific; both allogeneic and syngeneic cells being susceptible. Stimulation by LPS appears to be due to direct interaction between LPS and macrophages and does not involve participation by lymphocytes. After exposure to LPS, a latent period must elapse before macrophages can lyse tumor cells. The cytolytic mechanism requires contact between target cells and viable effector cells which maintain their lytic capacity for a sustained period and can kill on repeated occasions. The generation of a macrophage cytolytic effect by LPS is critically dependent upon the absolute number of macrophages which must be sufficient to produce confluent monolayers. These findings indicate that LPS stimulation of macrophages in vitro represents a valuable model system for the study of the mechanisms of macrophage stimulation and of the mediation of tumor cell death. The Rockefeller University Press 1978-08-01 /pmc/articles/PMC2184936/ /pubmed/568163 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
Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title_full Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title_fullStr Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title_full_unstemmed Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title_short Macrophage stimulation by bacterial lipopolysaccharides. I. Cytolytic effect on tumor target cells
title_sort macrophage stimulation by bacterial lipopolysaccharides. i. cytolytic effect on tumor target cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184936/
https://www.ncbi.nlm.nih.gov/pubmed/568163