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Cell Death Differ. 2016 Jan;23(1):76-88. doi: 10.1038/cdd.2015.70. Epub 2015 May 29.

Characterization of RIPK3-mediated phosphorylation of the activation loop of MLKL during necroptosis.

Author information

1
Department of Immunology, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
2
Department of Immunology, University of Washington, Seattle, WA 98109, USA.
3
Department Chemical Biology & Therapeutics, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
4
Institute for Cellular Therapeutics, University of Louisville, Louisville, KY 40202, USA.

Abstract

Mixed lineage kinase domain-like pseudokinase (MLKL) mediates necroptosis by translocating to the plasma membrane and inducing its rupture. The activation of MLKL occurs in a multimolecular complex (the 'necrosome'), which is comprised of MLKL, receptor-interacting serine/threonine kinase (RIPK)-3 (RIPK3) and, in some cases, RIPK1. Within this complex, RIPK3 phosphorylates the activation loop of MLKL, promoting conformational changes and allowing the formation of MLKL oligomers, which migrate to the plasma membrane. Previous studies suggested that RIPK3 could phosphorylate the murine MLKL activation loop at Ser345, Ser347 and Thr349. Moreover, substitution of the Ser345 for an aspartic acid creates a constitutively active MLKL, independent of RIPK3 function. Here we examine the role of each of these residues and found that the phosphorylation of Ser345 is critical for RIPK3-mediated necroptosis, Ser347 has a minor accessory role and Thr349 seems to be irrelevant. We generated a specific monoclonal antibody to detect phospho-Ser345 in murine cells. Using this antibody, a series of MLKL mutants and a novel RIPK3 inhibitor, we demonstrate that the phosphorylation of Ser345 is not required for the interaction between RIPK3 and MLKL in the necrosome, but is essential for MLKL translocation, accumulation in the plasma membrane, and consequent necroptosis.

PMID:
26024392
PMCID:
PMC4815980
DOI:
10.1038/cdd.2015.70
[Indexed for MEDLINE]
Free PMC Article

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