a Department of Cellular and Molecular Medicine , University of Ottawa , Ottawa , Ontario , Canada.
b Immunity and Inflammation , University of Ottawa Center for Infection , Ottawa , Canada.
Autophagy. 2019 Aug;15(8):1489-1491. doi: 10.1080/15548627.2019.1618640. Epub 2019 May 23.
Macroautophagy/autophagy is a conserved degradative pathway that host cells use to deal with invading pathogens. Despite significant overlap with starvation-induced autophagy, the early signaling that potentiates anti-bacterial autophagy is still unclear. Here we report AMPK, an upstream kinase regulating starvation-mediated autophagy induction, is activated in response to bacterial infection. AMPK inhibits MTORC1, an autophagy repressor, and activates autophagic ULK1 and PIK3C3/VPS34 complexes. Although AMPK-mediated inhibition of MTORC1 is not accompanied by the induction of bulk autophagy, AMPK regulation is critical for selectively targeting the bacteria for degradation. Moreover, AMPK signaling is triggered by the detection of bacteria-derived outer membrane vesicles and does not require bacterial invasion. Together, these data characterize and highlight the significance of AMPK signaling in priming the autophagic response to bacterial infection. AMPK: AMP-activated protein kinase; MTORC1: MTOR complex 1; ULK1: Unc-51 like kinase 1; PIK3C3/VPS34: Phosphatidylinositol 3-kinase catalytic subunit type 3.
自噬是一种保守的降解途径,宿主细胞利用它来应对入侵的病原体。尽管与饥饿诱导的自噬有很大的重叠,但增强抗细菌自噬的早期信号仍然不清楚。在这里,我们报告说,调节饥饿诱导的自噬诱导的上游激酶 AMPK,会对细菌感染产生反应而被激活。AMPK 抑制了 MTORC1,这是一种自噬抑制剂,并激活了自噬的 ULK1 和 PIK3C3/VPS34 复合物。虽然 AMPK 介导的 MTORC1 抑制并不伴随着大量自噬的诱导,但 AMPK 的调节对于选择性地将细菌靶向降解是至关重要的。此外,AMPK 信号是由细菌来源的外膜囊泡的检测触发的,并不需要细菌入侵。总之,这些数据描述并强调了 AMPK 信号在启动细菌感染的自噬反应中的重要性。