自噬
结肠炎
程序性细胞死亡
下调和上调
克洛丹
细胞生物学
肠上皮
地穴
泛素
癌症研究
生物
化学
上皮
免疫学
紧密连接
细胞凋亡
基因
生物化学
内分泌学
遗传学
作者
Rizwan Ahmad,Balawant Kumar,Raju Lama Tamang,Geoffrey A. Talmon,Punita Dhawan,Amar B. Singh
标识
DOI:10.1038/s42003-023-05116-2
摘要
Impaired autophagy promotes Inflammatory Bowel Disease (IBD). Claudin-2 is upregulated in IBD however its role in the pathobiology remains uncertain due to its complex regulation, including by autophagy. Irrespective, claudin-2 expression protects mice from DSS colitis. This study was undertaken to examine if an interplay between autophagy and claudin-2 protects from colitis and associated epithelial injury. Crypt culture and intestinal epithelial cells (IECs) are subjected to stress, including starvation or DSS, the chemical that induces colitis in-vivo. Autophagy flux, cell survival, co-immunoprecipitation, proximity ligation assay, and gene mutational studies are performed. These studies reveal that under colitis/stress conditions, claudin-2 undergoes polyubiquitination and P62/SQSTM1-assisted degradation through autophagy. Inhibiting autophagy-mediated claudin-2 degradation promotes cell death and thus suggest that claudin-2 degradation promotes autophagy flux to promote cell survival. Overall, these data inform for the previously undescribed role for claudin-2 in facilitating IECs survival under stress conditions, which can be harnessed for therapeutic advantages.
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