Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305-5125, USA.
Neuron. 2010 Mar 11;65(5):597-611. doi: 10.1016/j.neuron.2010.01.027.
To investigate the role of microRNAs in regulating oligodendrocyte (OL) differentiation and myelination, we utilized transgenic mice in which microRNA processing was disrupted in OL precursor cells (OPCs) and OLs by targeted deletion of Dicer1. We found that inhibition of OPC-OL miRNA processing disrupts normal CNS myelination and that OPCs lacking mature miRNAs fail to differentiate normally in vitro. We identified three miRNAs (miR-219, miR-138, and miR-338) that are induced 10-100x during OL differentiation; the most strongly induced of these, miR-219, is necessary and sufficient to promote OL differentiation, and partially rescues OL differentiation defects caused by total miRNA loss. miR-219 directly represses the expression of PDGFRalpha, Sox6, FoxJ3, and ZFP238 proteins, all of which normally help to promote OPC proliferation. Together, these findings show that miR-219 plays a critical role in coupling differentiation to proliferation arrest in the OL lineage, enabling the rapid transition from proliferating OPCs to myelinating OLs.
为了研究 microRNAs 在调控少突胶质细胞(OL)分化和髓鞘形成中的作用,我们利用转基因小鼠,通过靶向敲除 Dicer1 使 OL 前体细胞(OPC)和 OL 中的 microRNA 加工过程受到破坏。我们发现,抑制 OPC-OL microRNA 加工会破坏中枢神经系统的正常髓鞘形成,并且缺乏成熟 microRNAs 的 OPC 在体外无法正常分化。我们鉴定出三种在 OL 分化过程中诱导表达 10-100 倍的 microRNAs(miR-219、miR-138 和 miR-338);其中诱导表达最强的 miR-219 是促进 OL 分化所必需和充分的,并且可以部分挽救由总 microRNA 缺失引起的 OL 分化缺陷。miR-219 直接抑制 PDGFRalpha、Sox6、FoxJ3 和 ZFP238 蛋白的表达,所有这些蛋白通常都有助于促进 OPC 增殖。总之,这些发现表明 miR-219 在 OL 谱系中促进分化和增殖停滞的耦联中起着关键作用,使快速从增殖性 OPC 过渡到髓鞘形成的 OL 成为可能。