神经炎症
间充质干细胞
小胶质细胞
免疫系统
肿瘤坏死因子α
脂多糖
细胞生物学
炎症
体内
免疫学
神经科学
中枢神经系统
生物
癌症研究
医学
生物技术
作者
Yi Liu,Rong Zeng,Yezhong Wang,Wenhui Huang,Bin Hu,Guohui Zhu,Run Zhang,Feng Li,Jianbang Han,Yongshi Li
出处
期刊:Brain Research
[Elsevier]
日期:2019-12-01
卷期号:1724: 146422-146422
被引量:45
标识
DOI:10.1016/j.brainres.2019.146422
摘要
Microglia are the primary cells that exert immune function in the central nervous system (CNS), and they play an important role in the pathogenesis and progression of neuroinflammation-related diseases. Mesenchymal stem cells (MSCs) have been demonstrated to promote functional recovery in many neurological diseases. The mechanisms underlying this may be that MSCs can reduce inflammatory responses through various soluble factors. Among these factors, tumor necrosis factor-α-induced gene/protein 6 (TSG-6) is a key factor influencing MSCs immunomodulatory properties; however, the precise mechanisms underlying the anti-inflammatory effects are not fully understood. Here, we aim to investigate the potential effects of MSCs on neuroinflammation and to reveal the underlying mechanisms. First, we confirmed that administration of MSCs could inhibit the lipopolysaccharide (LPS)-induced neuroinflammatory responses in a mouse model. Then, we found that MSCs promoted M2 polarization and inhibited M1 polarization both in vivo and in vitro. Moreover, we demonstrated that the effect of MSCs on microglial polarization was dependent on TSG-6. This study demonstrated that MSCs promoted M2 polarization of microglia via TSG-6, thus conferring anti-neuroinflammatory effects.
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