Nitric oxide inhibits Fas-induced apoptosis

被引:276
作者
Mannick, JB
Miao, XQ
Stamler, JS
机构
[1] DUKE UNIV,MED CTR,HOWARD HUGHES MED INST,DEPT MED,DIV RESP,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,HOWARD HUGHES MED INST,DEPT MED,DIV CARDIOVASC MED,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,DEPT CELL BIOL,DURHAM,NC 27710
关键词
D O I
10.1074/jbc.272.39.24125
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 (CD95, APO-1) is a transmembrane cell surface receptor that mediates apoptosis of many cell types when bound by Fas ligand or cross-linked by agonist antibody. The cellular factors regulating Fas-induced apoptosis have not been well defined. Here we show that basal nitric-oxide synthase (NOS) activity in human leukocytes inhibits Fas-induced apoptosis via a cGMP-independent mechanism. Further, NOS inhibits Fas-induced cleavage of poly(ADP-ribose) polymerase by members of the caspase family of cysteine proteases. These data suggest that Fas activity is under the control of the NO signaling pathway. NOS regulating the function of this member of the tumor necrosis factor receptor family suggests a new role for nitric oxide (or related molecules) in the human immune response.
引用
收藏
页码:24125 / 24128
页数:4
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