自噬
生物
雅普1
细胞内
细胞生物学
内体
细胞外
金黄色葡萄球菌
胞浆
细胞内寄生虫
生物发生
细胞凋亡
转录因子
基因
生物化学
遗传学
细菌
酶
作者
Robin Caire,Nicola Pordone,Paul O. Verhoeven
出处
期刊:Autophagy
[Taylor & Francis]
日期:2023-02-21
卷期号:19 (10): 2811-2813
被引量:1
标识
DOI:10.1080/15548627.2023.2179771
摘要
Previously considered as an exclusive extracellular bacterium, Staphylococcus aureus has been shown to be able to invade many cells in vitro and in humans. Once inside the host cell, both cytosolic and endosome-associated S. aureus strongly induce macroautophagy/autophagy. Whether autophagy fosters S. aureus intracellular survival or clearance remains unclear. The YAP1-TEAD axis regulates the expression of target genes controlling the cell fate (e.g., proliferation, migration, cell cycle …). Growing evidence indicates that YAP1-TEAD also regulates autophagy and lysosomal pathways. Recently we showed that the YAP1-TEAD axis promotes autophagy and lysosome biogenesis to restrict S. aureus intracellular replication. We also discovered that the C3 exoenzyme-like EDIN-B toxin produced by the pathogenic S. aureus ST80 strain inhibits YAP1 nuclear translocation resulting in a strong increase of intracellular S. aureus burden.
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