摘要
MicroRNA(miRNA)已被确定为调节分化,增殖,炎症和自身免疫性疾病的各种生物过程中的关键参与者。新出现的证据表明miRNA在多发性硬化症(MS)发病机制中的关键作用。在这里,我们提供了miRNA的全面概述,miRNA在MS患者或实验性自身免疫性脑脊髓炎(EAE)小鼠中差异表达,并通过调节多种途径(包括CD4 + T细胞在CD4 + T细胞的三种亚型中的增殖,分化和活化)促进MS发病机制,包括Th1,Th17和调节性T细胞(Tregs)。此外,还描述了少突胶质细胞前体细胞(OPC)分化的调节作为MS发病机制的关键参与者。我们的文献研究表明,miR-223可以影响MS发病机制所涉及的不同途径,如促进Th1分化,激活骨髓细胞的M2表型,清除髓鞘碎片。MiR-223也被确定为一种潜在的生物标志物,可区分复发缓解型多发性硬化症(RRMS)和进行性多发性硬化症(PMS),因此,它可以作为进一步研究的有吸引力的靶标。我们的概述为治疗提供了新的潜在治疗靶点,并为miRNA在MS发病机制中的作用提供了新的见解。
关键词: 少突胶质细胞,Th1细胞,T调节细胞,Th17细胞,树突状细胞,microRNA
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