Shoubridge Andrew P, Fourrier Célia, Choo Jocelyn M, Proud Christopher G, Sargeant Timothy J, Rogers Geraint B
Microbiome and Host Health, Lifelong Health, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Infection and Immunity, Flinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
Front Microbiol. 2021 Dec 23;12:817433. doi: 10.3389/fmicb.2021.817433. eCollection 2021.
The gut microbiome-brain axis exerts considerable influence on the development and regulation of the central nervous system. Numerous pathways have been identified by which the gut microbiome communicates with the brain, falling largely into the two broad categories of neuronal innervation and immune-mediated mechanisms. We describe an additional route by which intestinal microbiology could mediate modifiable risk for neuropathology and neurodegeneration in particular. Autophagy, a ubiquitous cellular process involved in the prevention of cell damage and maintenance of effective cellular function, acts to clear and recycle cellular debris. In doing so, autophagy prevents the accumulation of toxic proteins and the development of neuroinflammation, both common features of dementia. Levels of autophagy are influenced by a range of extrinsic exposures, including nutrient deprivation, infection, and hypoxia. These relationships between exposures and rates of autophagy are likely to be mediated, as least in part, by the gut microbiome. For example, the suppression of histone acetylation by microbiome-derived short-chain fatty acids appears to be a major contributor to upregulation of autophagic function. We discuss the potential contribution of the microbiome-autophagy axis to neurological health and examine the potential of exploiting this link to predict and prevent neurodegenerative diseases.
肠道微生物群-脑轴对中枢神经系统的发育和调节具有相当大的影响。人们已经确定了许多肠道微生物群与大脑进行交流的途径,主要分为神经支配和免疫介导机制这两大类。我们描述了一种额外的途径,通过这种途径,肠道微生物学尤其可以介导神经病理学和神经退行性变的可改变风险。自噬是一种普遍存在的细胞过程,参与预防细胞损伤和维持有效的细胞功能,其作用是清除和循环利用细胞碎片。通过这样做,自噬可防止有毒蛋白质的积累和神经炎症的发展,而这两者都是痴呆症的常见特征。自噬水平受一系列外在暴露因素的影响,包括营养剥夺、感染和缺氧。这些暴露因素与自噬速率之间的关系可能至少部分是由肠道微生物群介导的。例如,微生物群衍生的短链脂肪酸对组蛋白乙酰化的抑制似乎是自噬功能上调的主要促成因素。我们讨论了微生物群-自噬轴对神经健康的潜在贡献,并研究了利用这种联系来预测和预防神经退行性疾病的潜力。