期刊
PLOS ONE
卷 9, 期 2, 页码 -出版社
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0089284
关键词
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资金
- NIH [AG032171, AI77780, AI77781, AI77782]
- NIH NAID [AI77782, AI096943bold]
- NIH/NIAID (HIV immune networks team, HINT) [AI77782, 1P01AI90935-01, 1R011AI073450-01A2, R01 AI089246bold]
- [1 P50 NIGMS085764-01A2]
Innate immune sensors such as Toll-like receptors (TLRs) differentially utilize adaptor proteins and additional molecular mediators to ensure robust and precise immune responses to pathogen challenge. Through a gain-of-function genetic screen, we identified the gamma catalytic subunit of protein phosphatase 1 (PP1-gamma) as a positive regulator of MyD88-dependent proinflammatory innate immune activation. PP1-gamma physically interacts with the E3 ubiquitin ligase TRAF6, and enhances the activity of TRAF6 towards itself and substrates such as IKK gamma, whereas enzymatically inactive PP1-gamma represses these events. Importantly, these activities were found to be critical for cellular innate responses to pathogen challenge and microbial clearance in both mouse macrophages and human monocyte lines. These data indicate that PP1-gamma phosphatase activity regulates overall TRAF6 E3 ubiquitin ligase function and promotes NF-kappa B-mediated innate signaling responses.
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