The YAP1-TEAD axis promotes autophagy against intracellular Staphylococcus aureus in vitro

被引:1
作者
Caire, Robin [1 ,2 ]
Pordone, Nicola [1 ,2 ]
Verhoeven, Paul O. [1 ,2 ,3 ,4 ]
机构
[1] Univ Lyon, Univ Claude Bernard Lyon 1, Ctr Int Rech Infectiol, GIMAP Team,CIRI,Inserm U1111,CNRS,UMR5308,ENS Lyon, Lyon, France
[2] Univ Jean Monnet St Etienne, Fac Med, St Etienne, France
[3] Univ Hosp St Etienne, Dept Infect Agents & Hyg, St Etienne, France
[4] Univ Lyon, Univ Claude Bernard Lyon 1, Ctr Int Rech Infectiol, GIMAP Team,CIRI,Inserm U1111,CNRS,ENS Lyon, Auvergne Rhone Alpes, France
关键词
Autophagy; C3; exoenzyme; cell-autonomous immunity; EDIN; host response genes; inflammation; lysosome; staphylococcus aureus; YAP;
D O I
10.1080/15548627.2023.2179771
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 horizontal ellipsis ). 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.
引用
收藏
页码:2811 / 2813
页数:3
相关论文
共 1 条
[1]   YAP promotes cell-autonomous immune responses to tackle intracellular Staphylococcus aureus in vitro [J].
Caire, Robin ;
Audoux, Estelle ;
Thomas, Mireille ;
Dalix, Elisa ;
Peyron, Aurelien ;
Rodriguez, Killian ;
Pordone, Nicola ;
Guillemot, Johann ;
Dickerscheit, Yann ;
Marotte, Hubert ;
Vandenesch, Francois ;
Laurent, Frederic ;
Josse, Jerome ;
Verhoeven, Paul O. .
NATURE COMMUNICATIONS, 2022, 13 (01)