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Ppm1b通过使Rip3去磷酸化来负向调节坏死性凋亡。

Ppm1b negatively regulates necroptosis through dephosphorylating Rip3.

作者信息

Chen Wanze, Wu Jianfeng, Li Lisheng, Zhang Zhengmao, Ren Junming, Liang Yaoji, Chen Fenfang, Yang Chao, Zhou Zhenru, Su Sheng Sean, Zheng Xinru, Zhang Zhirong, Zhong Chuan-Qi, Wan Haoqiang, Xiao Mu, Lin Xia, Feng Xin-Hua, Han Jiahuai

机构信息

State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361005, China.

1] Life Sciences Institute, and Innovation Center for Cell Signaling Network, Zhejiang University, Hangzhou, Zhejiang 310058, China [2] Department of Surgery, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Nat Cell Biol. 2015 Apr;17(4):434-44. doi: 10.1038/ncb3120. Epub 2015 Mar 9.

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.

摘要

坏死小体中鼠源受体相互作用蛋白3(Rip3)的苏氨酸231和丝氨酸232位点发生自磷酸化是触发坏死性凋亡所必需的。然而,Rip3磷酸化是如何被调控的在很大程度上仍不清楚。在此,我们鉴定出蛋白磷酸酶1B(Ppm1b)为Rip3磷酸酶,并发现Ppm1b在两种情况下限制坏死性凋亡:静息细胞中由Rip3自磷酸化引起的自发性坏死性凋亡,以及培养细胞中肿瘤坏死因子-α(TNF)诱导的坏死性凋亡。我们揭示Ppm1b通过使Rip3去磷酸化来选择性地抑制坏死性凋亡,进而阻止混合谱系激酶结构域样蛋白(Mlkl)募集到坏死小体。我们进一步表明,小鼠中的Ppm1b缺陷(Ppm1b(d/d))以Rip3依赖的方式增强了TNF诱导的死亡,并且在TNF处理的Ppm1b(d/d)小鼠的盲肠中,Rip3磷酸化水平升高和组织损伤证明了Ppm1b在抑制坏死性凋亡中的作用。这些数据表明,Ppm1b在体外和体内均通过使Rip3去磷酸化来负向调控坏死性凋亡。

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