Life in the Fas lane: differential outcomes of Fas signaling

被引:47
作者
Brint, Elizabeth [1 ]
O'Callaghan, Grace [2 ]
Houston, Aileen [2 ]
机构
[1] Natl Univ Ireland, Univ Coll Cork, Dept Pathol, Cork, Ireland
[2] Natl Univ Ireland, Univ Coll Cork, Dept Med, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
Fas/CD95; DISC; Apoptosis; NF-kappa B; Non-apoptotic; Regulation; NF-KAPPA-B; LIGAND-INDUCED APOPTOSIS; TUMOR-NECROSIS-FACTOR; FACTOR RECEPTOR SUPERFAMILY; ACTIVATED PROTEIN-KINASE; INDUCED IL-8 PRODUCTION; CD95; CO-STIMULATION; HUMAN T-LYMPHOCYTES; DEATH RECEPTOR; MEDIATED APOPTOSIS;
D O I
10.1007/s00018-013-1327-z
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
Fas, also known as CD95 or APO-1, is a member of the tumor necrosis factor/nerve growth factor superfamily. Although best characterized in terms of its apoptotic function, recent studies have identified several other cellular responses emanating from Fas. These responses include migration, invasion, inflammation, and proliferation. In this review, we focus on the diverse cellular outcomes of Fas signaling and the molecular switches identified to date that regulate its pro- and anti-apoptotic functions. Such switches occur at different levels of signal transduction, ranging from the receptor through to cross-talk with other signaling pathways. Factors identified to date including other extracellular signals, proteins recruited to the death-inducing signaling complex, and the availability of different intracellular components of signal transduction pathways. The success of therapeutically targeting Fas will require a better understanding of these pathways, as well as the regulatory mechanisms that determine cellular outcome following receptor activation.
引用
收藏
页码:4085 / 4099
页数:15
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