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Semin Immunol. 2014 Jun;26(3):246-52. doi: 10.1016/j.smim.2014.03.005. Epub 2014 May 21.

Functions of caspase 8: the identified and the mysterious.

Author information

1
Program in Cell Death and Survival Networks, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA. Electronic address: gsalvesen@sanfordburnham.org.
2
Department of Molecular Biology and Biochemistry, Institute for Immunology, University of California, Irvine, CA 92697, USA. Electronic address: cwalsh@uci.edu.

Abstract

Initially discovered as an initiator protease in apoptosis mediated by death receptors, caspase-8 is now known to have an apparently confounding opposing effect in securing cell survival. It is required to allow mouse embryo survival, and the survival of hematopoietic cells during their development and activation. Classic models in which caspase-8 is depleted or inhibited frequently result in inhibition of apoptosis, and conversion to death through a necrotic pathway. This bewildering switch is now known to be driven by activation of a pathway dependent on protein kinases of the RIP family, which engage a pathway known as necroptosis. If caspase-8 does not control this pathway, necrotic death results. The pro-apoptotic and pro-survival functions of caspase-8 are regulated by a specific interaction with the pseudo-caspase cFLIP, and it is thought that the heterocomplex between these two partners alters the substrate specificity of caspase-8 in favor of inactivating components of the RIP kinase pathway. The description of how caspase-8 and cFLIP coordinate the switch between apoptosis and survival is just beginning. The mechanism is not known, the differential targets are not known, and the reason of why an apoptotic initiator has been co-opted as a critical survival factor is only guessed at. Elucidating these unknowns will be important in understanding mechanisms and possible therapeutic targets in autoimmune, inflammatory, and metastatic diseases.

KEYWORDS:

Apoptosis; Autophagy; Necroptosis; Necrosis

PMID:
24856110
PMCID:
PMC4099255
DOI:
10.1016/j.smim.2014.03.005
[Indexed for MEDLINE]
Free PMC Article

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