Hyperosmotic stress induces metacaspase- and mitochondria-dependent apoptosis in Saccharomyces cerevisiae

被引:147
作者
Silva, RD
Sotoca, R
Johansson, B
Ludovico, P
Sansonetty, F
Silva, MT
Peinado, JM
Côrte-Real, M
机构
[1] Univ Minho, Ctr Biol, Dept Biol, P-4710057 Braga, Portugal
[2] Univ Complutense, Fac Biol, Dept Microbiol, E-28040 Madrid, Spain
[3] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, P-4710057 Braga, Portugal
[4] Univ Porto, IPATIMUP, Inst Patol & Imunol Mol, Lab Citometria, P-4200465 Oporto, Portugal
[5] Inst Biol Mol & Celular, P-4150180 Oporto, Portugal
关键词
D O I
10.1111/j.1365-2958.2005.04868.x
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
During the last years, several reports described an apoptosis-like programmed cell death process in yeast in response to different environmental aggressions. Here, evidence is presented that hyperosmotic stress caused by high glucose or sorbitol concentrations in culture medium induces in Saccharomyces cerevisiae a cell death process accompanied by morphological and biochemical indicators of apoptotic programmed cell death, namely chromatin condensation along the nuclear envelope, mitochondrial swelling and reduction of cristae number, production of reactive oxygen species and DNA strand breaks, with maintenance of plasma membrane integrity. Disruption of AIF1 had no effect on cell survival, but lack of Yca1p drastically reduced metacaspase activation and decreased cell death indicating that this death process was associated to activation of this protease. Supporting the involvement of mitochondria and cytochrome c in caspase activation, the mutant strains cyc1 Delta cyc7 Delta and cyc3 Delta, both lacking mature cytochrome c, displayed a decrease in caspase activation associated to increased cell survival when exposed to hyperosmotic stress. These findings indicate that hyperosmotic stress triggers S. cerevisiae into an apoptosis-like programmed cell death that is mediated by a caspase-dependent mitochondrial pathway partially dependent on cytochrome c.
引用
收藏
页码:824 / 834
页数:11
相关论文
共 45 条
[31]   Oxygen stress:: A regulator of apoptosis in yeast [J].
Madeo, F ;
Fröhlich, E ;
Ligr, M ;
Grey, M ;
Sigrist, SJ ;
Wolf, DH ;
Fröhlich, KU .
JOURNAL OF CELL BIOLOGY, 1999, 145 (04) :757-767
[32]   Release of cytochrome c and decrease of cytochrome c oxidase in Bax-expressing yeast cells, and prevention of these effects by coexpression of Bcl-x(L) [J].
Manon, S ;
Chaudhuri, B ;
Guerin, M .
FEBS LETTERS, 1997, 415 (01) :29-32
[33]   Insulin-like growth factor-I is an osmoprotectant in human neuroblastoma cells [J].
Matthews, CC ;
Odeh, HM ;
Feldman, EL .
NEUROSCIENCE, 1997, 79 (02) :525-534
[34]   IGF-1 regulates cardiac fibroblast apoptosis induced by osmotic stress [J].
Mockridge, JW ;
Benton, EC ;
Andreeva, LV ;
Latchman, DS ;
Marber, MS ;
Heads, RJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (01) :322-327
[35]   IGF-1 regulates apoptosis of cardiac myocyte induced by osmotic-stress [J].
Morales, MP ;
Gálvez, A ;
Eltit, JM ;
Ocaranza, P ;
Díaz-Araya, G ;
Lavandero, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 270 (03) :1029-1035
[36]   Role of mitochondria in the pheromone- and amiodarone-induced programmed death of yeast [J].
Pozniakovsky, AI ;
Knorre, DA ;
Markova, OV ;
Hyman, AA ;
Skulachev, VP ;
Severin, FF .
JOURNAL OF CELL BIOLOGY, 2005, 168 (02) :257-269
[37]   GLUCOSE REPRESSION OF CYTOCHROME ALPHA SYNTHESIS IN CYTOCHROME-DEFICIENT MUTANTS OF YEAST [J].
REILLY, C ;
SHERMAN, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1965, 95 (04) :640-&
[38]   Pheromone induces programmed cell death in S-cerevisiae [J].
Severin, FF ;
Hyman, AA .
CURRENT BIOLOGY, 2002, 12 (07) :R233-R235
[39]   INVIVO KILLING AND DEGRADATION OF MYCOBACTERIUM-AURUM WITHIN MOUSE PERITONEAL-MACROPHAGES [J].
SILVA, MT ;
APPELBERG, R ;
SILVA, MNT ;
MACEDO, PM .
INFECTION AND IMMUNITY, 1987, 55 (09) :2006-2016
[40]   Permeabilization of the mitochondrial inner membrane during apoptosis: impact of the adenine nucleotide translocator [J].
Vieira, HLA ;
Haouzi, D ;
El Hamel, C ;
Jacotot, E ;
Belzacq, AS ;
Brenner, C ;
Kroemer, G .
CELL DEATH AND DIFFERENTIATION, 2000, 7 (12) :1146-1154