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Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7

The Janus family of kinases (JAKs) has been shown to be involved in the signal transduction of a number of cytokine receptors. Recently, we have cloned a novel JAK family member, JAK3, that is expressed in natural killer and activated T cells and is coupled functionally and physically to the interle...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191962/
https://www.ncbi.nlm.nih.gov/pubmed/7535338
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description The Janus family of kinases (JAKs) has been shown to be involved in the signal transduction of a number of cytokine receptors. Recently, we have cloned a novel JAK family member, JAK3, that is expressed in natural killer and activated T cells and is coupled functionally and physically to the interleukin 2 (IL-2) receptor in these cells. Here we report that JAK3 was expressed at low but detectable levels in human monocytes. In contrast, JAK3 expression was strongly induced during activation by interferon gamma (IFN-gamma) or lipopolysaccharide. Moreover, JAK3 became tyrosine phosphorylated in response to IL-2, IL- 4, and IL-7 but not response to IFN-gamma or granulocyte/macrophage colony-stimulating factor. Together, these findings suggest that JAK3 is functionally important in activated monocytes and cells of the myeloid lineage and is involved in signaling responses of cytokines that use the common gamma-chain of the IL-2 receptor.
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spelling pubmed-21919622008-04-16 Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7 J Exp Med Articles The Janus family of kinases (JAKs) has been shown to be involved in the signal transduction of a number of cytokine receptors. Recently, we have cloned a novel JAK family member, JAK3, that is expressed in natural killer and activated T cells and is coupled functionally and physically to the interleukin 2 (IL-2) receptor in these cells. Here we report that JAK3 was expressed at low but detectable levels in human monocytes. In contrast, JAK3 expression was strongly induced during activation by interferon gamma (IFN-gamma) or lipopolysaccharide. Moreover, JAK3 became tyrosine phosphorylated in response to IL-2, IL- 4, and IL-7 but not response to IFN-gamma or granulocyte/macrophage colony-stimulating factor. Together, these findings suggest that JAK3 is functionally important in activated monocytes and cells of the myeloid lineage and is involved in signaling responses of cytokines that use the common gamma-chain of the IL-2 receptor. The Rockefeller University Press 1995-04-01 /pmc/articles/PMC2191962/ /pubmed/7535338 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
Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title_full Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title_fullStr Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title_full_unstemmed Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title_short Regulation of JAK3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
title_sort regulation of jak3 expression in human monocytes: phosphorylation in response to interleukins 2, 4, and 7
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191962/
https://www.ncbi.nlm.nih.gov/pubmed/7535338