已发表论文

细胞焦亡:肠道微生物群和多发性硬化之间的新联系

 

Authors Fan H, Shen R, Yan J , Bai Y, Fu Q, Shi X, Du G , Wang D

Received 27 August 2024

Accepted for publication 11 December 2024

Published 19 December 2024 Volume 2024:18 Pages 6145—6164

DOI https://doi.org/10.2147/DDDT.S489454

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Tuo Deng

Hua Fan,* Ruile Shen,* Junqiang Yan,* Yongjie Bai, Qizhi Fu, Xiaofei Shi, Ganqin Du, Dongmei Wang

The First Affiliated Hospital, College of Clinical Medicine, Henan University of Science and Technology, Luoyang, 471003, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Ganqin Du; Dongmei Wang, Email dgq99@163.com; wdmzgadyx@163.com

Abstract: This review elucidates the pivotal role of pyroptosis, triggered by gut microbiota, in the development of multiple sclerosis (MS), emphasizing its significance within the gut-brain axis. Our comprehensive analysis of recent literature reveals how dysbiosis in the gut microbiota of MS patients—characterized by reduced microbial diversity and shifts in bacterial populations—profoundly impacts immune regulation and the integrity of the central nervous system (CNS). Pyroptosis, an inflammatory form of programmed cell death, significantly exacerbates MS by promoting the release of inflammatory cytokines and causing substantial damage to CNS tissues. The gut microbiota facilitates this detrimental process through metabolites such as short-chain fatty acids and neuroactive compounds, or self-structural products like lipopolysaccharides (LPS), which modulate immune responses and influence neuronal survival. This review highlights the potential of modulating gut microbiota to regulate pyroptosis, thereby suggesting that targeting this pathway could be a promising therapeutic strategy to mitigate inflammatory responses and preserve neuronal integrity in patients with MS.

Keywords: multiple sclerosis, gut microbiota, pyroptosis, gut-brain axis, neuroinflammation, therapeutic targets