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Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes

We compared phagocytic and metabolic activities of multinucleated giant cells (MGC) and macrophages derived from human monocytes after 9-14 d in culture. Phagocytosis of sheep erythrocytes (E) coated with IgG, of E coated with IgM and complement, and of Candida albicans was comparable in MGC and mac...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187276/
https://www.ncbi.nlm.nih.gov/pubmed/6707580
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description We compared phagocytic and metabolic activities of multinucleated giant cells (MGC) and macrophages derived from human monocytes after 9-14 d in culture. Phagocytosis of sheep erythrocytes (E) coated with IgG, of E coated with IgM and complement, and of Candida albicans was comparable in MGC and macrophages. The same percentage of ingested fungi was killed by MGC (24 +/- 4%) and macrophages (21 +/- 5%). Approximately 70% of MGC and macrophages exhibited superoxide-dependent reduction of nitroblue tetrazolium during stimulation. Ia antigen was present on approximately 75% of both cell types. Analysis of cell populations separated by nuclear fluorescence indicated that beta- glucosaminidase, acid phosphatase, and beta-glucuronidase activity per cell was higher in MGC, but specific activity of these enzymes was greater in macrophages. These results suggest that MGC have the capacity to function like macrophages in host defense against infection.
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spelling pubmed-21872762008-04-17 Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes J Exp Med Articles We compared phagocytic and metabolic activities of multinucleated giant cells (MGC) and macrophages derived from human monocytes after 9-14 d in culture. Phagocytosis of sheep erythrocytes (E) coated with IgG, of E coated with IgM and complement, and of Candida albicans was comparable in MGC and macrophages. The same percentage of ingested fungi was killed by MGC (24 +/- 4%) and macrophages (21 +/- 5%). Approximately 70% of MGC and macrophages exhibited superoxide-dependent reduction of nitroblue tetrazolium during stimulation. Ia antigen was present on approximately 75% of both cell types. Analysis of cell populations separated by nuclear fluorescence indicated that beta- glucosaminidase, acid phosphatase, and beta-glucuronidase activity per cell was higher in MGC, but specific activity of these enzymes was greater in macrophages. These results suggest that MGC have the capacity to function like macrophages in host defense against infection. The Rockefeller University Press 1984-04-01 /pmc/articles/PMC2187276/ /pubmed/6707580 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
Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title_full Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title_fullStr Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title_full_unstemmed Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title_short Functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
title_sort functional and biochemical studies of multinucleated giant cells derived from the culture of human monocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187276/
https://www.ncbi.nlm.nih.gov/pubmed/6707580