Miao Yuxuan, Li Guojie, Zhang Xiaoli, Xu Haoxing, Abraham Soman N
Department of Molecular Genetics & Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Department of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Cell. 2015 Jun 4;161(6):1306-19. doi: 10.1016/j.cell.2015.05.009. Epub 2015 May 28.
Vertebrate cells have evolved elaborate cell-autonomous defense programs to monitor subcellular compartments for infection and to evoke counter-responses. These programs are activated by pathogen-associated pattern molecules and by various strategies intracellular pathogens employ to alter cellular microenvironments. Here, we show that, when uropathogenic E. coli (UPEC) infect bladder epithelial cells (BECs), they are targeted by autophagy but avoid degradation because of their capacity to neutralize lysosomal pH. This change is detected by mucolipin TRP channel 3 (TRPML3), a transient receptor potential cation channel localized to lysosomes. TRPML3 activation then spontaneously initiates lysosome exocytosis, resulting in expulsion of exosome-encased bacteria. These studies reveal a cellular default system for lysosome homeostasis that has been co-opted by the autonomous defense program to clear recalcitrant pathogens.
脊椎动物细胞已经进化出复杂的细胞自主防御程序,以监测亚细胞区室是否受到感染并引发相应的反应。这些程序由病原体相关模式分子以及细胞内病原体用于改变细胞微环境的各种策略激活。在这里,我们表明,当尿路致病性大肠杆菌(UPEC)感染膀胱上皮细胞(BECs)时,它们会被自噬靶向,但由于其中和溶酶体pH值的能力而避免被降解。这种变化由定位在溶酶体上的瞬时受体电位阳离子通道——黏脂质体TRP通道3(TRPML3)检测到。TRPML3激活随后自发启动溶酶体胞吐作用,导致包裹在外泌体中的细菌被排出。这些研究揭示了一种溶酶体稳态的细胞默认系统,该系统已被自主防御程序利用以清除顽固的病原体。