a Life Sciences Institute, University of Michigan , Ann Arbor , MI USA.
Autophagy. 2018;14(3):365-367. doi: 10.1080/15548627.2017.1401425. Epub 2018 Jan 29.
In 2013, Dr. Lora Hooper and colleagues described the induction of antibacterial macroautophagy/autophagy in intestinal epithelial cells as a cytoprotective host defense mechanism against invading Salmonella enterica serovar Typhimurium (S. Typhimurium). Canonical autophagy functions in a primarily degradative capacity to safeguard cells and ensure survival during stress conditions, including pathogen infection. In contrast, secretory autophagy has emerged as an alternative nondegradative mechanism for cellular trafficking and unconventional protein secretion. More recently, a study by Bel et al. from Dr. Hooper's lab describes how intestinal Paneth cells exploit the endoplasmic reticulum (ER) stress response to release antibacterial lysozyme through secretory autophagy in response to S. Typhimurium infection.
2013 年,Lora Hooper 博士及其同事描述了肠上皮细胞中抗菌巨自噬/自噬的诱导,这是一种针对侵袭性沙门氏菌肠炎亚种(S. Typhimurium)的细胞保护宿主防御机制。经典自噬主要在降解能力方面发挥作用,以在应激条件下(包括病原体感染)保护细胞并确保其存活。相比之下,分泌性自噬已成为细胞运输和非常规蛋白分泌的替代非降解机制。最近,Hooper 博士实验室的 Bel 等人的一项研究描述了肠 Paneth 细胞如何利用内质网(ER)应激反应来通过分泌性自噬释放抗菌溶菌酶,以响应 S. Typhimurium 感染。