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Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes

The product of the human IFN-gamma gene was found to be a powerful upregulatory stimulus for its own gene expression in lectin-activated human PBMC. The INF-gamma autosuperinduction response was further enhanced by "priming" PBMC with IFN-gamma. Primed cells maximally upregulated their lev...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189424/
https://www.ncbi.nlm.nih.gov/pubmed/2504874
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description The product of the human IFN-gamma gene was found to be a powerful upregulatory stimulus for its own gene expression in lectin-activated human PBMC. The INF-gamma autosuperinduction response was further enhanced by "priming" PBMC with IFN-gamma. Primed cells maximally upregulated their levels of IFN-gamma specific mRNA 4-fold faster and more than 20-fold higher than mock-stimulated cells. High mRNA levels persisted for several days after stimulation, and enhanced secretion of biologically active IFN-gamma paralleled the observed upregulation of gene expression. Producer cells demonstrating this response were found to be primarily localized to the rosette E- (leu 11+) fraction of PBMC and appear to be of the LGL/NK variety. Whether the autosuperinduction phenomenon occurs through direct or indirect effects of IFN-gamma on producer cells is still unclear. These results may be important both to an understanding of the pathogenesis of immune dysfunction and to the design of more effective immunotherapy.
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spelling pubmed-21894242008-04-17 Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes J Exp Med Articles The product of the human IFN-gamma gene was found to be a powerful upregulatory stimulus for its own gene expression in lectin-activated human PBMC. The INF-gamma autosuperinduction response was further enhanced by "priming" PBMC with IFN-gamma. Primed cells maximally upregulated their levels of IFN-gamma specific mRNA 4-fold faster and more than 20-fold higher than mock-stimulated cells. High mRNA levels persisted for several days after stimulation, and enhanced secretion of biologically active IFN-gamma paralleled the observed upregulation of gene expression. Producer cells demonstrating this response were found to be primarily localized to the rosette E- (leu 11+) fraction of PBMC and appear to be of the LGL/NK variety. Whether the autosuperinduction phenomenon occurs through direct or indirect effects of IFN-gamma on producer cells is still unclear. These results may be important both to an understanding of the pathogenesis of immune dysfunction and to the design of more effective immunotherapy. The Rockefeller University Press 1989-09-01 /pmc/articles/PMC2189424/ /pubmed/2504874 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
Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title_full Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title_fullStr Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title_full_unstemmed Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title_short Human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
title_sort human gamma interferon strongly upregulates its own gene expression in peripheral blood lymphocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189424/
https://www.ncbi.nlm.nih.gov/pubmed/2504874