Ji Jing, Sun Ya-Qin, Zha Zheng, Xue Bing, Li Jun-Ling, Jin Liang-Yun, Qi Fang, Zhang Nan, Zhao Hui, Fan Yong-Ping, Wang Lei
School of Traditional Chinese Medicine, Beijing Key Lab of TCM Collateral Disease Theory Research, Capital Medical University, Beijing, China.
College of Basic Medical Sciences, Hubei University of Chinese Medicine, Wuhan, China.
Evid Based Complement Alternat Med. 2022 Apr 13;2022:3341481. doi: 10.1155/2022/3341481. eCollection 2022.
Remyelination is a refractory feature of demyelinating diseases such as multiple sclerosis (MS). Studies have shown that promoting oligodendrocyte precursor cell (OPC) differentiation, which cannot be achieved by currently available therapeutic agents, is the key to enhancing remyelination. Bu Shen Yi Sui capsule (BSYSC) is a traditional Chinese herbal medicine over many years of clinical practice. We have found that BSYSC can effectively treat MS. In this study, the effects of BSYSC in promoting OPCs differentiation and remyelination were assessed using an experimental autoimmune encephalomyelitis (EAE) model in vivo and cultured OPCs in vitro. The results showed that BSYSC reduced clinical function scores and increased neuroprotection. The expression of platelet-derived growth factor receptor (PDGFR-) was decreased and the level of 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase) was increased in the brains and spinal cords of mice as well as in OPCs after treatment with BSYSC. We further found that BSYSC elevated the expression of miR-219 or miR-338 in the serum exosomes of mice with EAE, thereby suppressing the expression of Sox6, Lingo1, and Hes5, which negatively regulate OPCs differentiation. Therefore, serum exosomes of BSYSC-treated mice (exos-BSYSC) were extracted and administered to OPCs in which miR-219 or miR-338 expression was knocked down by adenovirus, and the results showed that Sox6, Lingo1, and Hes5 expression was downregulated, MBP expression was upregulated, OPCs differentiation was increased, and the ability of OPCs to wrap around neuronal axons was improved. In conclusion, BSYSC may exert clinically relevant effects by regulating microRNA (miR) levels in exosomes and thus promoting the differentiation and maturation of OPCs.
髓鞘再生是脱髓鞘疾病(如多发性硬化症,MS)的一个难治性特征。研究表明,促进少突胶质前体细胞(OPC)分化是增强髓鞘再生的关键,而目前可用的治疗药物无法实现这一点。补肾益髓胶囊(BSYSC)是一种经过多年临床实践的传统中药。我们发现BSYSC可有效治疗MS。在本研究中,使用体内实验性自身免疫性脑脊髓炎(EAE)模型和体外培养的OPC评估了BSYSC在促进OPC分化和髓鞘再生方面的作用。结果表明,BSYSC降低了临床功能评分并增强了神经保护作用。用BSYSC治疗后,小鼠脑和脊髓以及OPC中血小板衍生生长因子受体(PDGFR-)的表达降低,2',3'-环核苷酸3'-磷酸二酯酶(CNPase)的水平升高。我们进一步发现,BSYSC提高了EAE小鼠血清外泌体中miR-219或miR-338的表达,从而抑制了对OPC分化起负调节作用的Sox6、Lingo1和Hes5的表达。因此,提取了经BSYSC治疗的小鼠的血清外泌体(exos-BSYSC)并将其施用于通过腺病毒敲低miR-219或miR-338表达的OPC,结果显示Sox6、Lingo1和Hes5的表达下调,髓鞘碱性蛋白(MBP)表达上调,OPC分化增加,且OPC包裹神经元轴突的能力得到改善。总之,BSYSC可能通过调节外泌体中的微小RNA(miR)水平,从而促进OPC的分化和成熟发挥临床相关作用。