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Cell. 2014 May 8;157(4):897-909. doi: 10.1016/j.cell.2014.02.055.

The intrinsic apoptosis pathway mediates the pro-longevity response to mitochondrial ROS in C. elegans.

Author information

1
Department of Biology, McGill University, Montreal, QC H3A 1B1, Canada.
2
Department of Biology, McGill University, Montreal, QC H3A 1B1, Canada. Electronic address: siegfried.hekimi@mcgill.ca.

Abstract

The increased longevity of the C. elegans electron transport chain mutants isp-1 and nuo-6 is mediated by mitochondrial ROS (mtROS) signaling. Here we show that the mtROS signal is relayed by the conserved, mitochondria-associated, intrinsic apoptosis signaling pathway (CED-9/Bcl2, CED-4/Apaf1, and CED-3/Casp9) triggered by CED-13, an alternative BH3-only protein. Activation of the pathway by an elevation of mtROS does not affect apoptosis but protects from the consequences of mitochondrial dysfunction by triggering a unique pattern of gene expression that modulates stress sensitivity and promotes survival. In vertebrates, mtROS induce apoptosis through the intrinsic pathway to protect from severely damaged cells. Our observations in nematodes demonstrate that sensing of mtROS by the apoptotic pathway can, independently of apoptosis, elicit protective mechanisms that keep the organism alive under stressful conditions. This results in extended longevity when mtROS generation is inappropriately elevated. These findings clarify the relationships between mitochondria, ROS, apoptosis, and aging.

PMID:
24813612
PMCID:
PMC4454526
DOI:
10.1016/j.cell.2014.02.055
[Indexed for MEDLINE]
Free PMC Article

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