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Fas-mediated cytotoxicity by freshly isolated natural killer cells

The expression of Fas ligand on natural killer (NK) cells and Fas- mediated cytotoxicity by NK cells was investigated. Fas ligand mRNA was expressed in freshly isolated NK cells but not in T cells. Furthermore, the Fas ligand was detected on the cell surface of NK cells by staining with soluble Fas...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191925/
https://www.ncbi.nlm.nih.gov/pubmed/7532682
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collection PubMed
description The expression of Fas ligand on natural killer (NK) cells and Fas- mediated cytotoxicity by NK cells was investigated. Fas ligand mRNA was expressed in freshly isolated NK cells but not in T cells. Furthermore, the Fas ligand was detected on the cell surface of NK cells by staining with soluble Fas molecule. We analyzed the cytolytic activity of NK cells against thymocyte targets from normal and lpr mice, and found that the NK cells killed thymocytes from normal mice but not from lpr mice. On the other hand, splenic T cells did not show any cytotoxicity against either of the thymocyte targets. Similarly, NK cells exhibited cytotoxicity against transfectants expressing Fas antigen but not against parental cells or transfectants expressing a mutant Fas antigen with deleted cytoplasmic region. These results demonstrated that NK cells express Fas ligand and possess the capability of killing target cells expressing Fas antigen on their surface. This finding suggests that NK cells play an important role by eliminating Fas-expressing cells either constitutively or inducibly in peripheral lymphoid organs.
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spelling pubmed-21919252008-04-16 Fas-mediated cytotoxicity by freshly isolated natural killer cells J Exp Med Articles The expression of Fas ligand on natural killer (NK) cells and Fas- mediated cytotoxicity by NK cells was investigated. Fas ligand mRNA was expressed in freshly isolated NK cells but not in T cells. Furthermore, the Fas ligand was detected on the cell surface of NK cells by staining with soluble Fas molecule. We analyzed the cytolytic activity of NK cells against thymocyte targets from normal and lpr mice, and found that the NK cells killed thymocytes from normal mice but not from lpr mice. On the other hand, splenic T cells did not show any cytotoxicity against either of the thymocyte targets. Similarly, NK cells exhibited cytotoxicity against transfectants expressing Fas antigen but not against parental cells or transfectants expressing a mutant Fas antigen with deleted cytoplasmic region. These results demonstrated that NK cells express Fas ligand and possess the capability of killing target cells expressing Fas antigen on their surface. This finding suggests that NK cells play an important role by eliminating Fas-expressing cells either constitutively or inducibly in peripheral lymphoid organs. The Rockefeller University Press 1995-03-01 /pmc/articles/PMC2191925/ /pubmed/7532682 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
Fas-mediated cytotoxicity by freshly isolated natural killer cells
title Fas-mediated cytotoxicity by freshly isolated natural killer cells
title_full Fas-mediated cytotoxicity by freshly isolated natural killer cells
title_fullStr Fas-mediated cytotoxicity by freshly isolated natural killer cells
title_full_unstemmed Fas-mediated cytotoxicity by freshly isolated natural killer cells
title_short Fas-mediated cytotoxicity by freshly isolated natural killer cells
title_sort fas-mediated cytotoxicity by freshly isolated natural killer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191925/
https://www.ncbi.nlm.nih.gov/pubmed/7532682