Sato T, Irie S, Kitada S, Reed J C
La Jolla Cancer Research Foundation, Oncogene and Tumor Suppressor Gene Program, CA 92037, USA.
Science. 1995 Apr 21;268(5209):411-5. doi: 10.1126/science.7536343.
Fas is a cell surface receptor that controls a poorly understood signal transduction pathway that leads to cell death by means of apoptosis. A protein tyrosine phosphatase, FAP-1, capable of interacting with the cytosolic domain of Fas, was identified. The carboxyl terminal 15 amino acids of Fas are necessary and sufficient for interaction with FAP-1. FAP-1 expression is highest in tissues and cell lines that are relatively resistant to Fas-mediated cytotoxicity. Gene transfer-mediated elevations in FAP-1 partially abolished Fas-induced apoptosis in a T cell line. These findings are consistent with an inhibitory effect of FAP-1 on Fas signal transduction.
Fas是一种细胞表面受体,它控制着一条人们了解甚少的信号转导途径,该途径通过凋亡导致细胞死亡。一种能够与Fas胞质结构域相互作用的蛋白酪氨酸磷酸酶FAP-1被鉴定出来。Fas的羧基末端15个氨基酸对于与FAP-1的相互作用是必需且足够的。FAP-1在对Fas介导的细胞毒性相对抗性的组织和细胞系中表达最高。基因转移介导的FAP-1升高部分消除了T细胞系中Fas诱导的凋亡。这些发现与FAP-1对Fas信号转导的抑制作用一致。