Unknown

Dataset Information

0

Protein phosphatase 2A catalytic subunit ? plays a MyD88-dependent, central role in the gene-specific regulation of endotoxin tolerance.


ABSTRACT: MyD88, the intracellular adaptor of most TLRs, mediates either proinflammatory or immunosuppressive signaling that contributes to chronic inflammation-associated diseases. Although gene-specific chromatin modifications regulate inflammation, the role of MyD88 signaling in establishing such epigenetic landscapes under different inflammatory states remains elusive. Using quantitative proteomics to enumerate the inflammation-phenotypic constituents of the MyD88 interactome, we found that in endotoxin-tolerant macrophages, protein phosphatase 2A catalytic subunit ? (PP2Ac) enhances its association with MyD88 and is constitutively activated. Knockdown of PP2Ac prevents suppression of proinflammatory genes and resistance to apoptosis. Through site-specific dephosphorylation, constitutively active PP2Ac disrupts the signal-promoting TLR4-MyD88 complex and broadly suppresses the activities of multiple proinflammatory/proapoptotic pathways as well, shifting proinflammatory MyD88 signaling to a prosurvival mode. Constitutively active PP2Ac translocated with MyD88 into the nuclei of tolerant macrophages establishes the immunosuppressive pattern of chromatin modifications and represses chromatin remodeling to selectively silence proinflammatory genes, coordinating the MyD88-dependent inflammation control at both signaling and epigenetic levels under endotoxin-tolerant conditions.

SUBMITTER: Xie L 

PROVIDER: S-EPMC4060247 | biostudies-literature | 2013 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Protein phosphatase 2A catalytic subunit α plays a MyD88-dependent, central role in the gene-specific regulation of endotoxin tolerance.

Xie Ling L   Liu Cui C   Wang Li L   Gunawardena Harsha P HP   Yu Yanbao Y   Du Ruyun R   Taxman Debra J DJ   Dai Penggao P   Yan Zhen Z   Yu Jing J   Holly Stephen P SP   Parise Leslie V LV   Wan Yisong Y YY   Ting Jenny P JP   Chen Xian X  

Cell reports 20130221 3


MyD88, the intracellular adaptor of most TLRs, mediates either proinflammatory or immunosuppressive signaling that contributes to chronic inflammation-associated diseases. Although gene-specific chromatin modifications regulate inflammation, the role of MyD88 signaling in establishing such epigenetic landscapes under different inflammatory states remains elusive. Using quantitative proteomics to enumerate the inflammation-phenotypic constituents of the MyD88 interactome, we found that in endotox  ...[more]

Similar Datasets

| S-EPMC2802960 | biostudies-literature
| S-EPMC5173401 | biostudies-literature
2024-03-18 | PXD045779 | Pride
2021-12-01 | GSE181132 | GEO
| S-EPMC4916389 | biostudies-literature
| S-EPMC3281656 | biostudies-literature
| S-EPMC4187575 | biostudies-literature
| S-EPMC2881738 | biostudies-literature
| S-EPMC305778 | biostudies-literature
| S-EPMC4680974 | biostudies-literature