Institute for Immunology and School of Medicine, Tsinghua University, Beijing 100084, China; Beijing Key Laboratory for Immunological Research on Chronic Diseases, Tsinghua University, Beijing 100084, China.
Institute for Immunology and School of Medicine, Tsinghua University, Beijing 100084, China; Beijing Key Laboratory for Immunological Research on Chronic Diseases, Tsinghua University, Beijing 100084, China; Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing 100084, China.
Cell Host Microbe. 2019 May 8;25(5):706-718.e7. doi: 10.1016/j.chom.2019.03.012. Epub 2019 Apr 30.
Metabolic programs and host defense are highly integrated to ensure proper immune responses during stress. Central to these responses, mTOR regulates immune functions by sensing and integrating environmental cues, yet how these systems are coordinated at the intestinal surface remains undefined. We show that the antimicrobial peptide α-defensin is functionally sustained during nutrient deprivation because of regulation of the defensin-processing enzyme MMP7 by microbiota- and host-derived factors. Unlike other antimicrobial peptides, the MMP7-α-defensin axis remains active during nutrient fluctuations, providing essential protection against enteric pathogens. Sustained Mmp7 expression requires the microbiota and is mediated by de-repression of the transcription activator Atoh1 upon attenuation of the transcriptional repressor Hes1 in intestinal epithelial cells. Hes1 levels are regulated via mTOR and controlled translationally, constituting a metabolism-translation-transcription loop. Disrupting this loop by supplying nutrients paradoxically compromises antibacterial defense. Together, these results uncover a regulatory circuit that couples host nutrient status to epithelial antimicrobial immunity.
代谢程序和宿主防御高度整合,以确保在应激期间产生适当的免疫反应。mTOR 通过感应和整合环境线索来调节免疫功能,是这些反应的核心,但这些系统如何在肠道表面协调仍然不清楚。我们发现,由于微生物群和宿主来源的因子对防御素加工酶 MMP7 的调节,在营养缺乏期间,抗菌肽 α-防御素的功能得以维持。与其他抗菌肽不同,MMP7-α-防御素轴在营养波动期间仍然保持活跃,为肠道病原体提供了必要的保护。Mmp7 的持续表达需要微生物群,并且是通过在肠上皮细胞中转录抑制剂 Hes1 减弱时,转录激活因子 Atoh1 的去抑制介导的。Hes1 水平通过 mTOR 调节,并通过控制翻译进行控制,构成代谢-翻译-转录循环。通过供应营养物质来破坏这个循环,反而会损害抗菌防御。总之,这些结果揭示了一个将宿主营养状态与上皮抗菌免疫联系起来的调节回路。