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遗传证据表明,Nkx2.2 和 Pdgfra 是中枢神经系统发育中少突胶质细胞分化时间的主要决定因素。

Genetic evidence that Nkx2.2 and Pdgfra are major determinants of the timing of oligodendrocyte differentiation in the developing CNS.

机构信息

Department of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY 40292, USA.

出版信息

Development. 2014 Feb;141(3):548-55. doi: 10.1242/dev.095323.

Abstract

In the central nervous system (CNS), oligodendrocyte maturation and axonal myelination occur on a predictable schedule, but the underlying timing mechanisms are largely unknown. In the present study, we demonstrate that Nkx2.2 homeodomain transcription factor is a key regulator for the timing of oligodendrocyte differentiation during development. Whereas induced expression of Nkx2.2 in early oligodendrocyte precursor cells (OPCs) causes precocious differentiation of oligodendrocytes, conditional ablation of Nkx2.2 temporally delays oligodendrocyte maturation. Moreover, Nkx2.2 can directly bind to the promoter of platelet-derived growth factor receptor alpha (Pdgfra) and repress its gene expression. Genetic ablation of Pdgfra mimics the effect of Nkx2.2 overexpression in accelerating OPC differentiation in the developing spinal cord. Together, our findings strongly suggest that Nkx2.2 functions as a major 'switch' to turn off Pdgfra signaling in OPCs and initiate the intrinsic program for oligodendrocyte differentiation.

摘要

在中枢神经系统 (CNS) 中,少突胶质细胞的成熟和轴突髓鞘形成按照可预测的时间表进行,但潜在的时间机制在很大程度上尚不清楚。在本研究中,我们证明 Nkx2.2 同源域转录因子是发育过程中少突胶质细胞分化时间的关键调节因子。虽然诱导 Nkx2.2 在早期少突胶质前体细胞 (OPC) 中的表达会导致少突胶质细胞的早熟分化,但条件性敲除 Nkx2.2 会使少突胶质细胞成熟的时间暂时延迟。此外,Nkx2.2 可以直接与血小板衍生生长因子受体 alpha (Pdgfra) 的启动子结合并抑制其基因表达。Pdgfra 的基因敲除模拟了 Nkx2.2 过表达在加速发育中脊髓 OPC 分化的作用。总之,我们的研究结果强烈表明,Nkx2.2 作为一个主要的“开关”,可以关闭 OPC 中的 Pdgfra 信号,并启动少突胶质细胞分化的内在程序。

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