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探索小胶质细胞在肠-脑轴通讯中的作用:一项系统综述。

Exploring the Role of Microglial Cells in the Gut-Brain Axis Communication: A Systematic Review.

作者信息

Ortiz-Samur Nadia Suyin, Vijaya Akshay Kumar, Burokas Aurelijus, Mela Virginia

机构信息

Cell Biology, Genetics and Physiology (Cell Biology Division), Faculty of Sciences, Universidad de Málaga, Málaga, Spain.

Department of Biological Models, Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.

出版信息

J Neurochem. 2025 Jul;169(7):e70154. doi: 10.1111/jnc.70154.

Abstract

The gut-brain axis (GBA) is a bidirectional communication system between the gastrointestinal tract and the CNS, playing a key role in neurological function, immune response, and metabolism. Microglia, the resident immune cells in the brain, are crucial regulators of neuroinflammation and synaptic plasticity. Recent studies indicate that the gut microbiota modulates microglial activity through metabolic and immune pathways, with implications for neurodegenerative, neurodevelopmental, and psychiatric disorders. However, the mechanisms underlying microbiota-microglia interactions remain unclear. Following a systematic screening of 4481 studies, 20 preclinical studies met the inclusion criteria and were reviewed in depth to assess microbiota-microglia interactions. These studies were found by searching in PubMed, Science Direct, and Google Scholar. The findings synthesize results from 20 carefully selected studies examining the impact of gut microbiota on microglial function. Experimental models, including fecal microbiota transplantation, dietary interventions, and bacterial supplementation, were analyzed. Microglial activity was assessed through immunohistochemistry, gene expression profiling, and functional assays. Most studies suggest that gut dysbiosis promotes microglial overactivation and neuroinflammation through pathways involving microbial-derived short-chain fatty acids (SCFAs), bile acids, and neuroimmune signaling cascades such as TLR4/NF-κB and the NLRP3 inflammasomes, whereas microbiota-targeted interventions reduce inflammation and support cognitive function. Despite these promising findings, inconsistencies in study methodologies and microbiota analyses limit comparability and clinical translation. This review offers a unique synthesis of studies specifically linking gut microbiota alterations to microglial states, neuroinflammatory signatures, and cognitive outcomes across diverse experimental models. It highlights the therapeutic potential of microbiota-based strategies for modulating microglial function and mitigating neuroinflammatory diseases.

摘要

肠-脑轴(GBA)是胃肠道与中枢神经系统之间的双向通信系统,在神经功能、免疫反应和新陈代谢中起关键作用。小胶质细胞是大脑中的常驻免疫细胞,是神经炎症和突触可塑性的关键调节因子。最近的研究表明,肠道微生物群通过代谢和免疫途径调节小胶质细胞的活性,这对神经退行性疾病、神经发育障碍和精神疾病具有重要意义。然而,微生物群与小胶质细胞相互作用的潜在机制仍不清楚。在对4481项研究进行系统筛选后,有20项临床前研究符合纳入标准,并进行了深入审查,以评估微生物群与小胶质细胞的相互作用。这些研究是通过在PubMed、Science Direct和谷歌学术搜索中找到的。研究结果综合了20项精心挑选的研究结果,这些研究考察了肠道微生物群对小胶质细胞功能的影响。分析了包括粪便微生物群移植、饮食干预和细菌补充在内的实验模型。通过免疫组织化学、基因表达谱分析和功能测定来评估小胶质细胞的活性。大多数研究表明,肠道菌群失调通过涉及微生物衍生的短链脂肪酸(SCFAs)、胆汁酸以及TLR4/NF-κB和NLRP3炎性小体等神经免疫信号级联反应的途径促进小胶质细胞过度激活和神经炎症,而针对微生物群的干预措施则可减轻炎症并支持认知功能。尽管有这些有前景的发现,但研究方法和微生物群分析的不一致限制了可比性和临床转化。本综述对一系列不同实验模型中,将肠道微生物群改变与小胶质细胞状态、神经炎症特征和认知结果具体联系起来的研究进行了独特的综合。它强调了基于微生物群的策略在调节小胶质细胞功能和减轻神经炎症性疾病方面具有的治疗潜力。

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