某种肠道细菌
肠道菌群
外体
炎症
2型糖尿病
细菌外膜
细胞生物学
生物
IRS1
胰岛素抵抗
胰岛素
化学
糖尿病
微生物学
胰岛素受体
内分泌学
微泡
生物化学
免疫学
大肠杆菌
小RNA
基因
作者
Kumaran Sundaram,Yun Teng,Jingyao Mu,Qingbo Xu,Fangyi Xu,Mukesh K. Sriwastva,Lifeng Zhang,Juw Won Park,Xiang Zhang,Jun Yan,Shuang Qin Zhang,Michael L. Merchant,Shao‐yu Chen,Craig J. McClain,Gerald W. Dryden,Huang‐Ge Zhang
出处
期刊:Small
[Wiley]
日期:2024-01-15
被引量:4
标识
DOI:10.1002/smll.202308680
摘要
Abstract Gut microbiota function has numerous effects on humans and the diet humans consume has emerged as a pivotal determinant of gut microbiota function. Here, a new concept that gut microbiota can be trained by diet‐derived exosome‐like nanoparticles (ELNs) to release healthy outer membrane vesicles (OMVs) is introduced. Specifically, OMVs released from garlic ELN (GaELNs) trained human gut Akkermansia muciniphila ( A. muciniphila ) can reverse high‐fat diet‐induced type 2 diabetes (T2DM) in mice. Oral administration of OMVs released from GaELNs trained A. muciniphila can traffick to the brain where they are taken up by microglial cells, resulting in inhibition of high‐fat diet‐induced brain inflammation. GaELNs treatment increases the levels of OMV Amuc‐1100, P9, and phosphatidylcholines. Increasing the levels of Amuc‐1100 and P9 leads to increasing the GLP‐1 plasma level. Increasing the levels of phosphatidylcholines is required for inhibition of cGas and STING‐mediated inflammation and GLP‐1R crosstalk with the insulin pathway that leads to increasing expression of Insulin Receptor Substrate (IRS1 and IRS2) on OMV targeted cells. These findings reveal a molecular mechanism whereby OMVs from plant nanoparticle‐trained gut bacteria regulate genes expressed in the brain, and have implications for the treatment of brain dysfunction caused by a metabolic syndrome.
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