REGULATION OF JAK3 EXPRESSION IN HUMAN MONOCYTES - PHOSPHORYLATION IN RESPONSE TO INTERLEUKIN-2, INTERLEUKIN-4, AND INTERLEUKIN-7

被引:117
作者
MUSSO, T
JOHNSTON, JA
LINNEKIN, D
VARESIO, L
ROWE, TK
OSHEA, JJ
MCVICAR, DW
机构
[1] NCI, FREDERICK CANC RES & DEV CTR, EXPTL IMMUNOL LAB, FREDERICK, MD 21702 USA
[2] NCI, FREDERICK CANC RES & DEV CTR, LEUKOCYTE BIOL LAB, BIOL RESPONSE MODIFIERS PROGRAM, FREDERICK, MD 21702 USA
关键词
D O I
10.1084/jem.181.4.1425
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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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收藏
页码:1425 / 1431
页数:7
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