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

Qiang Zhu(University of Louisville), Xiaofeng Zhao(Hangzhou Normal University), Kang Zheng(Hangzhou Normal University), Hong Li(University of Louisville), Hao Huang(Hangzhou Normal University), Zunyi Zhang(Hangzhou Normal University), Teresa L. Mastracci(Columbia University), Michael Wegner(Friedrich-Alexander-Universität Erlangen-Nürnberg), Yiping Chen(Tulane University), Lori Sussel(Columbia University), Mengsheng Qiu(University of Louisville)
Development
January 21, 2014
Cited by 147Open Access
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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.


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