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Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates

Murine Kupffer cells (KC) were isolated by a high yield collagenase perfusion technique. The morphology, surface markers, and secretory products were typical of macrophages in other tissues. However, KC released negligible levels of H2O2 and O-2, in contrast to peritoneal macrophages. KC oxygen cons...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187591/
https://www.ncbi.nlm.nih.gov/pubmed/3921651
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description Murine Kupffer cells (KC) were isolated by a high yield collagenase perfusion technique. The morphology, surface markers, and secretory products were typical of macrophages in other tissues. However, KC released negligible levels of H2O2 and O-2, in contrast to peritoneal macrophages. KC oxygen consumption was not increased by agents triggering a respiratory burst in peritoneal cells. Moreover, KC capacity to secrete reactive oxygen intermediates (ROI), in contrast to Ia antigen expression, was not enhanced by exposure to lymphokines or recombinant gamma interferon. The selective defect in KC oxidative response was paralleled by impaired in vitro killing of Toxoplasma gondii trophozoites and Leishmania donovani promastigotes and amastigotes. Deficient secretion of ROI by KC might protect hepatocytes and erythrocytes from injury during endocytosis by KC, but might render the liver more susceptible to parasitization by organisms that are primarily killed through oxygen-dependent mechanisms.
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spelling pubmed-21875912008-04-17 Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates J Exp Med Articles Murine Kupffer cells (KC) were isolated by a high yield collagenase perfusion technique. The morphology, surface markers, and secretory products were typical of macrophages in other tissues. However, KC released negligible levels of H2O2 and O-2, in contrast to peritoneal macrophages. KC oxygen consumption was not increased by agents triggering a respiratory burst in peritoneal cells. Moreover, KC capacity to secrete reactive oxygen intermediates (ROI), in contrast to Ia antigen expression, was not enhanced by exposure to lymphokines or recombinant gamma interferon. The selective defect in KC oxidative response was paralleled by impaired in vitro killing of Toxoplasma gondii trophozoites and Leishmania donovani promastigotes and amastigotes. Deficient secretion of ROI by KC might protect hepatocytes and erythrocytes from injury during endocytosis by KC, but might render the liver more susceptible to parasitization by organisms that are primarily killed through oxygen-dependent mechanisms. The Rockefeller University Press 1985-05-01 /pmc/articles/PMC2187591/ /pubmed/3921651 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
Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title_full Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title_fullStr Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title_full_unstemmed Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title_short Murine Kupffer cells. Mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
title_sort murine kupffer cells. mononuclear phagocytes deficient in the generation of reactive oxygen intermediates
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187591/
https://www.ncbi.nlm.nih.gov/pubmed/3921651