| Literature DB >> 25751141 |
Wanze Chen1, Jianfeng Wu1, Lisheng Li1, Zhengmao Zhang2, Junming Ren1, Yaoji Liang1, Fenfang Chen3, Chao Yang1, Zhenru Zhou1, Sheng Sean Su1, Xinru Zheng1, Zhirong Zhang1, Chuan-Qi Zhong1, Haoqiang Wan1, Mu Xiao3, Xia Lin4, Xin-Hua Feng2, Jiahuai Han1.
Abstract
The auto-phosphorylation of murine receptor-interacting protein 3 (Rip3) on Thr 231 and Ser 232 in the necrosome is required to trigger necroptosis. However, how Rip3 phosphorylation is regulated is still largely unknown. Here we identified protein phosphatase 1B (Ppm1b) as a Rip3 phosphatase and found that Ppm1b restricts necroptosis in two settings: spontaneous necroptosis caused by Rip3 auto-phosphorylation in resting cells, and tumour necrosis factor-α (TNF)-induced necroptosis in cultured cells. We revealed that Ppm1b selectively suppresses necroptosis through the dephosphorylation of Rip3, which then prevents the recruitment of mixed lineage kinase domain-like protein (Mlkl) to the necrosome. We further showed that Ppm1b deficiency (Ppm1b(d/d)) in mice enhanced TNF-induced death in a Rip3-dependent manner, and the role of Ppm1b in inhibiting necroptosis was evidenced by elevated Rip3 phosphorylation and tissue damage in the caecum of TNF-treated Ppm1b(d/d) mice. These data indicate that Ppm1b negatively regulates necroptosis through dephosphorylating Rip3 in vitro and in vivo.Entities:
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Year: 2015 PMID: 25751141 PMCID: PMC4523090 DOI: 10.1038/ncb3120
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824