Delgado Mónica A, Elmaoued Rasha A, Davis Alexander S, Kyei George, Deretic Vojo
Department of Molecular Genetics and Microbiology, University of New Mexico, Health Sciences Center, Albuquerque, NM 87131, USA.
EMBO J. 2008 Apr 9;27(7):1110-21. doi: 10.1038/emboj.2008.31. Epub 2008 Mar 13.
Autophagy is a newly recognized innate defense mechanism, acting as a cell-autonomous system for elimination of intracellular pathogens. The signals and signalling pathways inducing autophagy in response to pathogen invasion are presently not known. Here we show that autophagy is controlled by recognizing conserved pathogen-associated molecular patterns (PAMPs). We screened a PAMP library for effects on autophagy in RAW 264.7 macrophages and found that several prototype Toll-like receptor (TLR) ligands induced autophagy. Single-stranded RNA and TLR7 generated the most potent effects. Induction of autophagy via TLR7 depended on MyD88 expression. Stimulation of autophagy with TLR7 ligands was functional in eliminating intracellular microbes, even when the target pathogen was normally not associated with TLR7 signalling. These findings link two innate immunity defense systems, TLR signalling and autophagy, provide a potential molecular mechanism for induction of autophagy in response to pathogen invasion, and show that the newly recognized ability of TLR ligands to stimulate autophagy can be used to treat intracellular pathogens.
自噬是一种新发现的固有防御机制,作为一种细胞自主系统用于清除细胞内病原体。目前尚不清楚响应病原体入侵诱导自噬的信号和信号通路。在此我们表明,自噬是通过识别保守的病原体相关分子模式(PAMP)来控制的。我们筛选了一个PAMP文库以研究其对RAW 264.7巨噬细胞自噬的影响,发现几种典型的Toll样受体(TLR)配体可诱导自噬。单链RNA和TLR7产生的效应最为显著。通过TLR7诱导自噬依赖于MyD88的表达。用TLR7配体刺激自噬在消除细胞内微生物方面具有功能,即使目标病原体通常与TLR7信号传导无关。这些发现将两个固有免疫防御系统,即TLR信号传导和自噬联系起来,为响应病原体入侵诱导自噬提供了一种潜在的分子机制,并表明新认识到的TLR配体刺激自噬的能力可用于治疗细胞内病原体。