肠-脑轴
线粒体
炎症
肠道菌群
小胶质细胞
免疫系统
生物
肠神经系统
失调
平衡
神经炎症
免疫学
发病机制
神经科学
细胞生物学
作者
Yi Wang,Han Lai,Tian Zhang,Jing Wu,Huiling Tang,Xuanwei Liang,Dandan Ren,Jinzhu Huang,Weihong Li
标识
DOI:10.1016/j.neubiorev.2023.105403
摘要
The role of gut dysbiosis in depression is well established. However, recent studies have shown that gut microbiota is regulated by intestinal epithelial cell (IEC) mitochondria, which has yet to receive much attention. This review summarizes the recent developments about the critical role of IEC mitochondria in actively maintaining gut microbiota, intestinal metabolism, and immune homeostasis. We propose that IEC mitochondrial dysfunction alters gut microbiota composition, participates in cell fate, mediates oxidative stress, activates the peripheral immune system, causes peripheral inflammation, and transmits peripheral signals through the vagus and enteric nervous systems. These pathological alterations lead to brain inflammation, disruption of the blood-brain barrier, activation of the hypothalamic-pituitary-adrenal axis, activation of microglia and astrocytes, induction of neuronal loss, and ultimately depression. Furthermore, we highlight the prospect of treating depression through the mitochondria of IECs. These new findings suggest that the mitochondria of IECs may be a newly found important factor in the pathogenesis of depression and represent a potential new strategy for treating depression.
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