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Nat Rev Immunol. 2014 Sep;14(9):601-18. doi: 10.1038/nri3720.

A long-awaited merger of the pathways mediating host defence and programmed cell death.

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1
Immunology Institute and Tisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.

Abstract

Historically, cell death and inflammation have been closely linked, but the necessary divergence of the fields in the past few decades has enriched our molecular understanding of the signalling pathways that mediate various programmes of cell death and multiple types of inflammatory responses. The fields have now come together again demonstrating a surprising level of integration. Intimate interconnections at multiple levels are revealed between the cell death and inflammatory signal transduction pathways that are mobilized in response to the engagement of pattern recognition receptors during microbial infection. Molecules such as receptor-interacting protein kinase 1 (RIPK1), RIPK3, FAS-associated death domain protein (FADD), FLICE-like inhibitory protein (FLIP) and caspase 8 - which are associated with different forms of cell death - are incorporated into compatible and exceedingly dynamic Toll-like receptor, NOD-like receptor and RIG-I-like receptor signalling modules. These signalling modules have a high capacity to switch from inflammation to cell death, or a programmed execution of both, all in an orchestrated battle for host defence and survival.

PMID:
25145756
DOI:
10.1038/nri3720
[Indexed for MEDLINE]

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