癌变
程序性细胞死亡
生物
细胞生物学
癌症研究
癌症
细胞凋亡
遗传学
作者
Rajendra Karki,Balamurugan Sundaram,Bhesh Raj Sharma,SangJoon Lee,R. K. Subbarao Malireddi,Lam Nhat Nguyen,Shelbi Christgen,Min Zheng,Yaqiu Wang,Parimal Samir,Geoffrey Neale,Peter Vogel,Thirumala‐Devi Kanneganti
出处
期刊:Cell Reports
[Elsevier]
日期:2021-10-01
卷期号:37 (3): 109858-109858
被引量:218
标识
DOI:10.1016/j.celrep.2021.109858
摘要
Cell death provides host defense and maintains homeostasis. Zα-containing molecules are essential for these processes. Z-DNA binding protein 1 (ZBP1) activates inflammatory cell death, PANoptosis, whereas adenosine deaminase acting on RNA 1 (ADAR1) serves as an RNA editor to maintain homeostasis. Here, we identify and characterize ADAR1's interaction with ZBP1, defining its role in cell death regulation and tumorigenesis. Combining interferons (IFNs) and nuclear export inhibitors (NEIs) activates ZBP1-dependent PANoptosis. ADAR1 suppresses this PANoptosis by interacting with the Zα2 domain of ZBP1 to limit ZBP1 and RIPK3 interactions. Adar1
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