TGF-beta inhibits IL-2-induced tyrosine phosphorylation and activation of Jak-1 and Stat 5 in T lymphocytes

被引:0
|
作者
Bright, JJ
Kerr, LD
Sriram, S
机构
[1] VANDERBILT UNIV, MED CTR, DEPT NEUROL, NASHVILLE, TN 37212 USA
[2] VANDERBILT UNIV, MED CTR, DEPT MICROBIOL IMMUNOL, NASHVILLE, TN 37212 USA
来源
JOURNAL OF IMMUNOLOGY | 1997年 / 159卷 / 01期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signaling through IL-2R, IL-2 induces tyrosine phosphorylation and activation of Jak-1 and Jak-3 kinases and Stat 3 and Stat 5 transcription factors leading to cell cycle progression of activated T cells from G(1) to S phase. TGF-beta is an immunosuppressive cytokine, which inhibits T cell proliferation at G(1) to S phase transition. We examined the effect of TGF-beta on IL-2R signal transduction pathway in activated T cells. We show here that treatment of activated T cells with TGF-beta inhibited IL-2-induced tyrosine phosphorylation and activation of Jak-1 and Stat 5 but not Jak-3 and Stat 3. TGF-beta also inhibited IL-2-induced expression of alpha- and beta-chains of IL-2R and induced apoptotic cell death in T cells. These results suggest that TGF-beta-induced growth arrest and apoptosis are associated with the modulation of IL-2-induced activation of ak-Stat pathway in T cells.
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页码:175 / 183
页数:9
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