Loss of peroxisome function triggers necrosis

被引:47
作者
Jungwirth, Helmut [1 ]
Ring, Julia [1 ]
Mayer, Tanja [1 ]
Schauer, Alexandra [1 ]
Buettner, Sabrina [1 ]
Eisenberg, Tobias [1 ]
Carmona-Gutierrez, Didac [1 ]
Kuchler, Karl [2 ]
Madeo, Frank [1 ]
机构
[1] Graz Univ, IMB, A-8010 Graz, Austria
[2] Med Univ Vienna, Max F Perutz Labs, Christian Doppler Lab Infect Biol, A-1030 Vienna, Austria
基金
奥地利科学基金会;
关键词
peroxins; PEX6; acetic acid; stationary phase; necrosis;
D O I
10.1016/j.febslet.2008.07.023
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
Disturbance of peroxisome function can lead to various degenerative diseases during ageing. Here, we show that in yeast deletion of PEX6, encoding a protein involved in a key step of peroxisomal protein import, results in an increased accumulation of reactive oxygen species and an enhanced loss of viability upon acetic acid treatment and during early stationary phase. Cell death of ageing-like yeast cells lacking PEX6 does not depend on the apoptotic key players Yca1p and Aif1p, but instead shows markers of necrosis. Thus, we conclude that loss of peroxisomal function leads to a form of necrotic cell death. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:2882 / 2886
页数:5
相关论文
共 39 条
[1]   Pex8p:: An intraperioxisomal organizer of the peroxisomal import machinery [J].
Agne, B ;
Meindl, NM ;
Niederhoff, K ;
Einwächter, H ;
Rehling, P ;
Sickmann, A ;
Meyer, HE ;
Girzalsky, W ;
Kunau, WH .
MOLECULAR CELL, 2003, 11 (03) :635-646
[2]   Peroxisome biogenesis and the role of protein import [J].
Brown, LA ;
Baker, A .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (04) :388-400
[3]   Functional mitochondria are required for α-synuclein toxicity in aging yeast [J].
Buettner, Sabrina ;
Bitto, Alessandro ;
Ring, Julia ;
Augsten, Manuela ;
Zabrocki, Piotr ;
Eisenberg, Tobias ;
Jungwirth, Helmut ;
Hutter, Sylvia ;
Carmona-Gutierrez, Didac ;
Kroemer, Guido ;
Winderickx, Joris ;
Madeo, Frank .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (12) :7554-7560
[4]  
Chang CC, 1999, J CELL SCI, V112, P1579
[5]   The peroxisome biogenesis factors Pex4p, Pex22p, Pex1p, and Pex6p act in the terminal steps of peroxisomal matrix protein import [J].
Collins, CS ;
Kalish, JE ;
Morrell, JC ;
McCaffery, JM ;
Gould, SJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7516-7526
[6]   Unified nomenclature for peroxisome biogenesis factors [J].
Distel, B ;
Erdmann, R ;
Gould, SJ ;
Blobel, G ;
Crane, DI ;
Cregg, JM ;
Dodt, G ;
Fujiki, Y ;
Goodman, JM ;
Just, WW ;
Kiel, JAKW ;
Kunau, WH ;
Lazarow, PB ;
Mannaerts, GP ;
Moser, HW ;
Osumi, T ;
Rachubinski, RA ;
Roscher, A ;
Subramani, S ;
Tabak, HF ;
Tsukamoto, T ;
Valle, D ;
vanderKlei, I ;
vanVeldhoven, PP ;
Veenhuis, M .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :1-3
[7]   Peroxisome biogenesis [J].
Eckert, JH ;
Erdmann, R .
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, VOL 147 2003, 2003, 147 :75-121
[8]   Chronological aging-independent replicative life span regulation by Msn2/Msn4 and Sod2 in Saccharomyces cerevisiae [J].
Fabrizio, P ;
Pletcher, SD ;
Minois, N ;
Vaupel, JW ;
Longo, VD .
FEBS LETTERS, 2004, 557 (1-3) :136-142
[9]   The chronological life span of Saccharomyces cerevisiae [J].
Fabrizio, P ;
Longo, VD .
AGING CELL, 2003, 2 (02) :73-81
[10]   Cell death by necrosis: towards a molecular definition [J].
Golstein, Pierre ;
Kroemer, Guido .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (01) :37-43