Han Bing, Sivaramakrishnan Priya, Lin Chih-Chun J, Neve Isaiah A A, He Jingquan, Tay Li Wei Rachel, Sowa Jessica N, Sizovs Antons, Du Guangwei, Wang Jin, Herman Christophe, Wang Meng C
Huffington Center on Aging, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Cell. 2017 Jun 15;169(7):1249-1262.e13. doi: 10.1016/j.cell.2017.05.036.
Homeostasis of the gut microbiota critically influences host health and aging. Developing genetically engineered probiotics holds great promise as a new therapeutic paradigm to promote healthy aging. Here, through screening 3,983 Escherichia coli mutants, we discovered that 29 bacterial genes, when deleted, increase longevity in the host Caenorhabditis elegans. A dozen of these bacterial mutants also protect the host from age-related progression of tumor growth and amyloid-beta accumulation. Mechanistically, we discovered that five bacterial mutants promote longevity through increased secretion of the polysaccharide colanic acid (CA), which regulates mitochondrial dynamics and unfolded protein response (UPR) in the host. Purified CA polymers are sufficient to promote longevity via ATFS-1, the host UPR-responsive transcription factor. Furthermore, the mitochondrial changes and longevity effects induced by CA are conserved across different species. Together, our results identified molecular targets for developing pro-longevity microbes and a bacterial metabolite acting on host mitochondria to promote longevity.
肠道微生物群的稳态对宿主健康和衰老有着至关重要的影响。开发基因工程益生菌作为促进健康衰老的新治疗模式具有巨大潜力。在这里,通过筛选3983个大肠杆菌突变体,我们发现有29个细菌基因缺失时会延长宿主秀丽隐杆线虫的寿命。其中十几个细菌突变体还能保护宿主免受与年龄相关的肿瘤生长进展和β-淀粉样蛋白积累的影响。从机制上讲,我们发现五个细菌突变体通过增加多糖结肠酸(CA)的分泌来促进长寿,CA可调节宿主线粒体动力学和未折叠蛋白反应(UPR)。纯化的CA聚合物足以通过宿主UPR反应性转录因子ATFS-1来促进长寿。此外,CA诱导的线粒体变化和长寿效应在不同物种中是保守的。总之,我们的结果确定了开发长寿微生物的分子靶点以及一种作用于宿主线粒体以促进长寿的细菌代谢物。