A physical interaction between the cell death protein Fas and the tyrosine kinase p59(fynT)

被引:77
|
作者
Atkinson, EA
Ostergaard, H
Kane, K
Pinkoski, MJ
Caputo, A
Olszowy, MW
Bleackley, RC
机构
[1] UNIV ALBERTA, DEPT BIOCHEM, EDMONTON, AB T6G 2H7, CANADA
[2] UNIV ALBERTA, DEPT IMMUNOL, EDMONTON, AB T6G 2H7, CANADA
[3] WASHINGTON UNIV, SCH MED, CTR IMMUNOL, ST LOUIS, MO 63110 USA
[4] WASHINGTON UNIV, SCH MED, DEPT PATHOL, ST LOUIS, MO 63110 USA
关键词
D O I
10.1074/jbc.271.11.5968
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
The Fas antigen (Apol/CD95) is a transmembrane protein belonging to the nerve growth factor receptor family. It is expressed on a variety of cells, including activated T lymphocytes. Ligation of Fas with its natural ligand or with anti-Fas antibodies often results in the apoptotic death of the cell, making Fas an important mediator of down-regulating immune responses. The signal transduction pathways utilized by Fas are currently unknown, although tyrosine kinase activity has recently been strongly implicated. Here, we report that the tyrosine kinase p59(fyn) physically associates with Fas in Fas sensitive cells. In addition, we show that activated T lymphocytes from fyn knockout mice exhibit elevated lifespans and reduced apoptosis in vitro compared to their normal counterparts. Furthermore, activated T lymphocytes from the fyn- deficient mice are less sensitive to killing by both anti-Fas antibody and Fas-ligand cytotoxic T cells. These results suggest that p59(fyn) plays an important role in Fas signal transduction.
引用
收藏
页码:5968 / 5971
页数:4
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