A common set of engulfment genes mediates removal of both apoptotic and necrotic cell corpses in C-elegans

被引:126
作者
Chung, SB
Gumienny, TL
Hengartner, MO
Driscoll, M
机构
[1] Rutgers State Univ, Nelson Biol Labs, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[3] SUNY Stony Brook, Genet Program, Stony Brook, NY 11794 USA
关键词
D O I
10.1038/35046585
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Similar to mammalian excitotoxic cell death, necrotic-like cell death (NCD) in Caenorhabditis elegans can be initiated by hyperactive ion channels. Here we investigate the requirements for genes that execute and regulate programmed cell death (PCD) in necrotic-like neuronal death caused by a toxic MEG-4 channel. Neither the kinetics of necrosis onset nor the total number of necrotic corpses generated is altered by any C. elegans mutation known to block PCD, which provides genetic evidence that, the activating mechanisms for NCD and apoptotic cell death are distinct. In contrast, all previously reported ced genes required for phagocytotic removal of apoptotic corpses, as well as ced-12, a new engulfment gene we have identified, are required for efficient elimination of corpses generated by distinct necrosis-inducing stimuli. Our results show that a common set of genes acts to eliminate cell corpses irrespective of the mode of cell death, and provide the first identification of the C. elegans genes that are required for orderly removal of necrotic cells. As phagocytotic mechanisms seem to be conserved from nematodes to humans, our findings indicate that injured necrotic cells in higher organisms might also be eliminated before lysis through a controlled process of corpse removal, a hypothesis that has significant therapeutic implications.
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收藏
页码:931 / 937
页数:7
相关论文
共 51 条
[1]   A CELL THAT DIES DURING WILD-TYPE C-ELEGANS DEVELOPMENT CAN FUNCTION AS A NEURON IN A CED-3 MUTANT [J].
AVERY, L ;
HORVITZ, HR .
CELL, 1987, 51 (06) :1071-1078
[2]  
Barger AJ, 1998, J NEUROSCI, V18, P2871
[3]  
BRENNER S, 1974, GENETICS, V77, P71
[4]   Constitutive death of platelets leading to scavenger receptor-mediated phagocytosis - A caspase-independent cell clearance program [J].
Brown, SB ;
Clarke, MCH ;
Magowan, L ;
Sanderson, H ;
Savill, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (08) :5987-5996
[5]   THE IDENTIFICATION AND SUPPRESSION OF INHERITED NEURODEGENERATION IN CAENORHABDITIS-ELEGANS [J].
CHALFIE, M ;
WOLINSKY, E .
NATURE, 1990, 345 (6274) :410-416
[6]   DEVELOPMENTAL GENETICS OF THE MECHANOSENSORY NEURONS OF CAENORHABDITIS-ELEGANS [J].
CHALFIE, M ;
SULSTON, J .
DEVELOPMENTAL BIOLOGY, 1981, 82 (02) :358-370
[7]   Interdigital cell death can occur through a necrotic and caspase-independent pathway [J].
Chautan, M ;
Chazal, G ;
Cecconi, F ;
Gruss, P ;
Golstein, P .
CURRENT BIOLOGY, 1999, 9 (17) :967-970
[8]   The C-elegans protein EGL-1 is required for programmed cell death and interacts with the Bcl-2-like protein CED-9 [J].
Conradt, B ;
Horvitz, HR .
CELL, 1998, 93 (04) :519-529
[9]   THE MEC-4 GENE IS A MEMBER OF A FAMILY OF CAENORHABDITIS-ELEGANS GENES THAT CAN MUTATE TO INDUCE NEURONAL DEGENERATION [J].
DRISCOLL, M ;
CHALFIE, M .
NATURE, 1991, 349 (6310) :588-593
[10]  
DRISCOLL M, 1995, METHOD CELL BIOL, V46, P323