外体
间充质干细胞
骨髓
细胞生物学
微泡
干细胞
生物
医学
化学
免疫学
小RNA
生物化学
基因
作者
Hua Liu,Xuejun Yan,Jing Hu,Pan Hu,Xiao Mao,Yong Cheng
标识
DOI:10.1016/j.brainresbull.2025.111527
摘要
Major depressive disorder (MDD) is a multifaceted mental disorder marked by a spectrum of significant and persistent low mood symptoms. Its etiology involves genetic and environmental factors. In addition, the inflammatory process plays a crucial role in the pathophysiology of depression. Exosomes derived from bone marrow mesenchymal stem cells (BMSCs) have demonstrated significant effects in reducing proinflammatory cytokines. However, there is limited research on whether exosomes can prevent the occurrence of LPS-induced depression. This study aimed to investigate the role of BMSC-derived exosomes in LPS-induced depression and explore the underlying mechanisms. We administered exosomes to LPS-induced depression mice via the caudal vein and evaluated their effects on depressive-like behaviors. Our findings indicate that four injections of exosomes (200µl at a concentration of 1.4×10¹¹ particles/ml, administered every three days) significantly prevented depressive-like behaviors in LPS-induced depression mice. Further analyses revealed that exosome treatment reduced levels of pro-inflammatory cytokines (IL-1β, IL-6, TNF-α) and increased anti-inflammatory cytokine IL-10. Additionally, exosome treatment markedly reduced oxidative stress in both the central and peripheral nervous systems of LPS-treated mice. Moreover, our data suggest that exosome treatment increased astrocyte proliferation and neurogenesis in the hippocampus of LPS mice. In summary, our results demonstrate the antidepressant effects of BMSC-derived exosomes in LPS-induced depression mice, suggesting a potential new therapeutic target for major depressive disorder (MDD).
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