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诱导MST2磷酸化,介导河马信号通路的激活,以促进细胞凋亡和肺组织损伤。

induces MST2 phosphorylation mediating the activation of hippo signaling pathway to promote apoptosis and lung tissue damage.

作者信息

Xu Kangzhi, Zhu Shifan, Xu Fan, Yang Jin, Deng Bin, Su Dingzeyang, Ma Jing, Zu Mingyue, Lin Yifan, Pei Tianxu, Zhu Yuyang, Wang Lele, Liu Dandan, Duan Qiangde, Xu Jinjun, Pan Zhiming, Tao Jianping, Hou Zhaofeng

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou 225009, China.

出版信息

iScience. 2024 Nov 4;27(12):111312. doi: 10.1016/j.isci.2024.111312. eCollection 2024 Dec 20.

Abstract

() is an intracellular parasite, and its regulation of host cell apoptosis directly affects its parasitism. Studies link -induced apoptosis to abnormal expression of mammalian STE20-like protein kinase 2 (MST2), but its precise role remains unclear. In this study, the regulatory roles in apoptosis and pathogenicity of infection were identified and . Simultaneously, MST2 and Hippo signaling pathway activation induced by were evaluated. MST2 overexpression and knockout were used to assess its regulatory role in apoptosis and Hippo signaling pathway. Results showed that induced apoptosis and lung damage, with Hippo signaling pathway activation via MST2 phosphorylation. MST2 was demonstrated to regulate apoptosis and Hippo signaling pathway. Notably, MST2 knockout hindered the -induced apoptosis and weakened Hippo signaling pathway activation. MST2 is an important target for to control host cell fate and modulate immune responses.

摘要

()是一种细胞内寄生虫,其对宿主细胞凋亡的调控直接影响其寄生。研究将 - 诱导的凋亡与哺乳动物STE20样蛋白激酶2(MST2)的异常表达联系起来,但其确切作用仍不清楚。在本研究中,确定了 感染在凋亡和致病性中的调控作用 以及 。同时,评估了 诱导的MST2和Hippo信号通路激活。使用MST2过表达和敲除来评估其在凋亡和Hippo信号通路中的调控作用。结果表明, 诱导凋亡和肺损伤,通过MST2磷酸化激活Hippo信号通路。证明MST2调节凋亡和Hippo信号通路。值得注意的是,MST2敲除阻碍了 - 诱导的凋亡并减弱了Hippo信号通路激活。MST2是 控制宿主细胞命运和调节免疫反应的重要靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f3/11618000/1deaa686f291/fx1.jpg

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