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鹿茸间充质干细胞外泌体通过抑制TLR2/TLR4信号通路改善体外循环大鼠术后认知功能障碍

Exosomes of Antler Mesenchymal Stem Cells Improve Postoperative Cognitive Dysfunction in Cardiopulmonary Bypass Rats through Inhibiting the TLR2/TLR4 Signaling Pathway.

作者信息

Yang Chun, Sun Shengnan, Zhang Qi, Guo Jia, Wu Tengfei, Liu Ying, Yang Min, Zhang Yan, Peng Yinghua

机构信息

Institute of Special Wild Economic Animal and Plants, Chinese Academy of Agricultural Sciences, Changchun, China.

State Key Laboratory for Molecular Biology of Special Economic Animal, Changchun, China.

出版信息

Stem Cells Int. 2020 Mar 26;2020:2134565. doi: 10.1155/2020/2134565. eCollection 2020.

Abstract

Postoperative cognitive dysfunction (POCD) is a severe complication of cardiopulmonary bypass (CPB) and has common characteristics such as acute cognitive dysfunction, impaired memory, and inattention. Mesenchymal stem cells (MSCs) are multipotent cells that have therapeutic potentials mainly through paracrine action via secreting growth factors and cytokines. Exosomes are one of the important paracrine factors and have been reported as potential cell-free therapy for the treatment of autoimmune and central nervous system disorders. In this study, we examined exosomes derived from antler MSCs (AMSCs) of POCD rats after CPB and evaluated their potential regulatory mechanisms. AMSC-derived exosomes reduced neurological damage and brain damage and prevent apoptosis in CPB rats. Furthermore, AMSC-derived exosomes were found to reduce hippocampal neuronal apoptosis and the expression of TLR2, TLR4, MyD88, and NF-B in CPB rats. However, the above effects of AMSC-derived exosomes on CPB rats were abolished partially by toll-like receptor 2/4 (TLR2/TLR4) agonist (LPS-EB). In conclusion, AMSC-derived exosomes can improve cognitive function in CPB rats through inhibiting the TLR2/TLR4 signaling pathway.

摘要

术后认知功能障碍(POCD)是体外循环(CPB)的一种严重并发症,具有急性认知功能障碍、记忆力受损和注意力不集中等共同特征。间充质干细胞(MSCs)是多能细胞,主要通过分泌生长因子和细胞因子的旁分泌作用发挥治疗潜力。外泌体是重要的旁分泌因子之一,已被报道作为潜在的无细胞疗法用于治疗自身免疫性疾病和中枢神经系统疾病。在本研究中,我们检测了CPB后POCD大鼠鹿茸间充质干细胞(AMSCs)来源的外泌体,并评估了其潜在的调节机制。AMSC来源的外泌体减少了CPB大鼠的神经损伤和脑损伤,并预防了细胞凋亡。此外,发现AMSC来源的外泌体可减少CPB大鼠海马神经元凋亡以及TLR2、TLR4、MyD88和NF-κB的表达。然而,AMSC来源的外泌体对CPB大鼠的上述作用被Toll样受体2/4(TLR2/TLR4)激动剂(LPS-EB)部分消除。总之,AMSC来源的外泌体可通过抑制TLR2/TLR4信号通路改善CPB大鼠的认知功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6de0/7136781/012f7ad9243b/SCI2020-2134565.001.jpg

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