Inhibition of Fas-induced apoptotic cell death by osmotic cell shrinkage

被引:30
作者
Gulbins, E
Welsch, J
LeppleWienhuis, A
Heinle, H
Lang, F
机构
[1] Department of Physiology, University of Tuebingen, 72076 Tuebingen
关键词
D O I
10.1006/bbrc.1997.6775
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
Apoptosis is an active physiological mechanism permitting the elimination of cells by triggering an intracellular signalling cascade, Here, we tested whether osmotic alterations of cell volume interfere with apoptotic cell death in Jurkat T-lymphocytes. Apoptotic cell death of Jurkat cells was elicited by activation of the Fas receptor which results in sphingomyelinase stimulation, release of ceramide, activation of Ras, Rac-proteins and formation of O-2(-). Osmotic cell shrinkage inhibited apoptotic cell death induced by the Fas receptor in Jurkat T-lymphocytes. Osmotic cell shrinkage did not interfere with Fas induced activation of the acidic sphingomyelinase or activation of Ras but impaired the formation of O-2(-) suggesting an important function of cell volume in the synthesis of reactive oxygen intermediates upon Fas receptor ligation. (C) 1991 Academic Press.
引用
收藏
页码:517 / 521
页数:5
相关论文
共 29 条
[1]   Absence of volume regulatory mechanisms contributes to the rapid activation of apoptosis in thymocytes [J].
Bortner, CD ;
Cidlowski, JA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (03) :C950-C961
[2]  
BORTNER CD, 1995, J CELL BIOCHEM, P268
[3]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[4]   Fas-mediated apoptosis is modulated by intracellular glutathione in human T cells [J].
Chiba, T ;
Takahashi, S ;
Sato, N ;
Ishii, S ;
Kikuchi, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (05) :1164-1169
[5]   Superoxide anion is a natural inhibitor of Fas-mediated cell death [J].
Clement, MV ;
Stamenkovic, I .
EMBO JOURNAL, 1996, 15 (02) :216-225
[6]   FAS-INDUCED APOPTOSIS IS MEDIATED VIA A CERAMIDE-INITIATED RAS SIGNALING PATHWAY [J].
GULBINS, E ;
BISSONNETTE, R ;
MAHBOUBI, A ;
MARTIN, S ;
NISHIOKA, W ;
BRUNNER, T ;
BAIER, G ;
BAIERBITTERLICH, G ;
BYRD, C ;
LANG, F ;
KOLESNICK, R ;
ALTMAN, A ;
GREEN, D .
IMMUNITY, 1995, 2 (04) :341-351
[7]   Fas-induced apoptosis is mediated by activation of a Ras and Rac protein-regulated signaling pathway [J].
Gulbins, E ;
Coggeshall, KM ;
Brenner, B ;
Schlottmann, K ;
Linderkamp, O ;
Lang, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :26389-26394
[8]   Fas-induced programmed cell death is mediated by a Ras-regulated O-2(-) synthesis [J].
Gulbins, E ;
Brenner, B ;
Schlottmann, K ;
Welsch, J ;
Heinle, H ;
Koppenhoefer, U ;
Lindekamp, O ;
Coggeshall, KM ;
Lang, F .
IMMUNOLOGY, 1996, 89 (02) :205-212
[9]   CELL-VOLUME AND HORMONE ACTION [J].
HAUSSINGER, D ;
LANG, F .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1992, 13 (10) :371-373
[10]   OVEREXPRESSION OF MITOCHONDRIAL MANGANESE SUPEROXIDE-DISMUTASE PROMOTES THE SURVIVAL OF TUMOR-CELLS EXPOSED TO INTERLEUKIN-1, TUMOR-NECROSIS-FACTOR, SELECTED ANTICANCER DRUGS, AND IONIZING-RADIATION [J].
HIROSE, K ;
LONGO, DL ;
OPPENHEIM, JJ ;
MATSUSHIMA, K .
FASEB JOURNAL, 1993, 7 (02) :361-368