CD95/Fas/Apo-1-mediated signal transduction

被引:13
作者
Schlottmann, K [1 ]
Coggeshall, KM [1 ]
机构
[1] OHIO STATE UNIV, DEPT MICROBIOL, COLUMBUS, OH 43210 USA
关键词
Fas; Apo-1; CD95; signal transduction;
D O I
10.1159/000154838
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Fas/Apo-1/CD95 (Fas) receptor plays an important role in a variety of cellular systems via regulation of apoptotic cell death as, e.g., in lymphoid cells. Involvement of the Fas receptor in the pathogenesis of diseases such as AIDS, hepatitis and cancer has recently been postulated. The intracellular signal generated by the Fas receptor has been intensively studied during the past years and a wide variety of different molecules and signalling mechanisms have been implicated in the transduction of the death signal. However, there is evidence that triggering Fas does not only induce apoptosis but also stimulates mitogenic signals for cell activation and proliferation. Therefore, not all signalling components which have been detected after crosslinking the Fas receptor necessarily have to be related to the death signal. Furthermore, the recognition that apoptosis induced through activation of Fas is not protein synthesis dependent suggests that processes as the activation of transcription factors like NF-kappa B are most likely part of the stimulatory/mitogenic signal. Thus, signalling components of the Fas receptor are complex and have to be investigated carefully in terms of the outcome of the transmitted signal.
引用
收藏
页码:345 / 360
页数:16
相关论文
共 149 条
[81]   FAS-BASED D10S-MEDIATED CYTOTOXICITY REQUIRES MACROMOLECULAR-SYNTHESIS FOR EFFECTOR CELL ACTIVATION BUT NOT FOR TARGET-CELL DEATH [J].
LUCIANI, MF ;
GOLSTEIN, P .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1994, 345 (1313) :303-309
[82]   FAS AND FASL IN THE HOMEOSTATIC REGULATION OF IMMUNE-RESPONSES [J].
LYNCH, DH ;
RAMSDELL, F ;
ALDERSON, MR .
IMMUNOLOGY TODAY, 1995, 16 (12) :569-574
[83]   MOLECULAR-CLONING OF A NOVEL PROTEIN-TYROSINE-PHOSPHATASE CONTAINING A MEMBRANE-BINDING DOMAIN AND GLGF REPEATS [J].
MAEKAWA, K ;
IMAGAWA, N ;
NAGAMATSU, M ;
HARADA, S .
FEBS LETTERS, 1994, 337 (02) :200-206
[84]   APO-1 MEDIATED APOPTOSIS OR PROLIFERATION IN HUMAN CHRONIC B-LYMPHOCYTIC LEUKEMIA - CORRELATION WITH BCL-2 ONCOGENE EXPRESSION [J].
MAPARA, MY ;
BARGOU, R ;
ZUGCK, C ;
DOHNER, H ;
USTAOGLU, F ;
JONKER, RR ;
KRAMMER, PH ;
DORKEN, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (03) :702-708
[85]   PROTEASE ACTIVATION DURING APOPTOSIS - DEATH BY 1000 CUTS [J].
MARTIN, SJ ;
GREEN, DR .
CELL, 1995, 82 (03) :349-352
[86]   Small stress proteins as novel regulators of apoptosis - Heat shock protein 27 blocks Fas/APO-1- and staurosporine-induced cell death [J].
Mehlen, P ;
SchulzeOsthoff, K ;
Arrigo, AP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16510-16514
[87]   Events in apoptosis - Acidification is downstream of protease activation and BCL-2 protection [J].
Meisenholder, GW ;
Martin, SJ ;
Green, DR ;
Nordberg, J ;
Babior, BM ;
Gottlieb, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (27) :16260-16262
[88]  
MEMON SA, 1995, J IMMUNOL, V155, P4644
[89]   C-JUN N-TERMINAL PHOSPHORYLATION CORRELATES WITH ACTIVATION OF THE JNK SUBGROUP BUT NOT THE ERK SUBGROUP OF MITOGEN-ACTIVATED PROTEIN-KINASES [J].
MINDEN, A ;
LIN, AN ;
SMEAL, T ;
DERIJARD, B ;
COBB, M ;
DAVIS, R ;
KARIN, M .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (10) :6683-6688
[90]   SRC KINASE ASSOCIATES WITH A MEMBER OF A DISTINCT SUBFAMILY OF PROTEIN-TYROSINE PHOSPHATASES CONTAINING AN EZRIN-LIKE DOMAIN [J].
MOLLER, NPH ;
MOLLER, KB ;
LAMMERS, R ;
KHARITONENKOV, A ;
SURES, I ;
ULLRICH, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7477-7481