Role of insulin receptor substrate-2 in interleukin-9-dependent proliferation

被引:16
作者
Demoulin, JB
Grasso, L
Atkins, JM
Stevens, M
Louahed, J
Levitt, RC
Nicolaides, NC
Renauld, JC
机构
[1] Catholic Univ Louvain, Ludwig Inst Canc Res, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Expt Med Unit, B-1200 Brussels, Belgium
[3] Magainin Pharmaceut Inc, Magainin Inst Mol Med, Plymouth Meeting, PA 19462 USA
来源
FEBS LETTERS | 2000年 / 482卷 / 03期
关键词
interleukin-9; proliferation; apoptosis; insulin receptor substrate; protein kinase B;
D O I
10.1016/S0014-5793(00)02059-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-9 (IL-9) stimulation results in JAK, STAT and IRS1/2 phosphorylation. The role of IRS adaptor proteins in IL-9 signaling is not clear. We show that IL-9 induces IRS2 phosphorylation and association with phosphatidylinositol-3 kinase (PI 3-K) p85 subunit in TS1 cells and BaF/9R cells. which proliferate upon IL-9 stimulation. We observed a PI 3-K-dependent phosphorylation of protein kinase B (PKB) in TS1 cells, but not in BaF/9R, nor in other IL-9-dependent cell lines. Finally, 32D cells that were transfected with the IL-9 receptor but lack IRS expression survived in the presence of IL-9. Ectopic IRS1 expression allowed for IL-9-Induced proliferation, in the absence of significant PKB phosphorylation. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:200 / 204
页数:5
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