Analysis of the role of MKK-4/Sek-1 in T cell development and apoptosis

被引:5
作者
Alberola-Ila, J
Levin, SD
Barton, G
Forbush, K
Zon, LI
Perlmutter, RM
机构
[1] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[4] Univ Washington, Dept Med Med Genet, Seattle, WA 98195 USA
[5] Merck & Co Inc, Merck Sharp & Dohme Res Labs, Rahway, NJ 07065 USA
[6] Childrens Hosp, Boston, MA 02115 USA
关键词
apoptosis; dominant-negative transgene; Fas; thymic development; stress-activated protein; kinase;
D O I
10.1093/intimm/10.8.1077
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 stress-activated protein kinases (SAPK) are a group of dual-specificity kinases with potential roles in the control of apoptosis and proliferation. In most cells they are regulated through phosphorylation by MKK-4. We have investigated the role of MKK-4 in T cell development and function by generating transgenic animals expressing catalytically inactive MKK-4 (dMKK-4) in the thymus. Our results show that overexpression of dMKK-4 does not interfere with normal T cell development. Furthermore, expression of dMKK-4 inhibits Fas- but not phorbol ester plus ionomycin-induced activation of SAPK, suggesting that a SAPK kinase different from MKK-4 is responsible for the regulation of SAPK activation after stimulation of T cells with phorbol ester plus ionomycin. We then analyzed the effect of dMKK-4 on Fas-induced apoptosis of thymocytes. Our results show that activation of SAPK is not a necessary event in Fas-induced apoptosis of thymocytes.
引用
收藏
页码:1077 / 1082
页数:6
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