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A TRP Channel Senses Lysosome Neutralization by Pathogens to Trigger Their Expulsion

机译:TRP通道感知病原体的溶酶体中和作用以触发其驱逐

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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 lyso-somes. 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.
机译:脊椎动物细胞已经进化出完善的细胞自主防御程序,以监测亚细胞区室的感染情况并引起对策。这些程序被病原体相关的模式分子和细胞内病原体用来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(BEC)时,它们被自噬靶向,但由于其能中和溶酶体pH值而避免了降解。这种变化是通过粘蛋白TRP通道3(TRPML3)检测到的,该通道是位于溶酶体的瞬时受体电位阳离子通道。然后,TRPML3激活自发地启动溶酶体的胞吐作用,从而导致包裹有囊泡的细菌被排出。这些研究揭示了溶酶体内稳态的细胞默认系统,该系统已被自主防御计划选择来清除顽固病原体。

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