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Sox10 directs neural stem cells toward the oligodendrocyte lineage by decreasing Suppressor of Fused expression

机译:Sox10通过降低融合表达抑制因子将神经干细胞引向少突胶质细胞系

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摘要

Oligodendrocyte precursor cells (OPCs) are lineage-restricted progenitors generally limited in vivo to producing oligodendrocytes. Mechanisms controlling genesis of OPCs are of interest because of their importance in myelin development and their potential for regenerative therapies in multiple sclerosis and dysmyelinating syndromes. We show here that the SoxE transcription factors (comprising Sox8, 9, and 10) induce multipotent neural precursor cells (NPCs) from the early postnatal subventricular zone (SVZ) to become OPCs in an autonomous manner. We performed a chromatin immunoprecipitation-based bioinformatic screen and identified Suppressor of Fused (Sufu) as a direct target of repression by Sox10. In vitro, overexpression of Sufu blocked OPC production, whereas RNAi-mediated inhibition augmented OPC production. Furthermore, mice heterozygous for Sufu have increased numbers of OPCs in the telencephalon during development. We conclude that Sox10 acts to restrict the potential of NPCs toward the oligodendrocyte lineage in part by regulating the expression of Sufu.
机译:少突胶质前体细胞(OPC)是沿袭限制祖细胞,通常在体内仅限于产生少突胶质细胞。控制OPC发生的机制之所以引起人们的兴趣,是因为它们在髓鞘形成中的重要性以及在多发性硬化症和髓鞘异常综合征中进行再生治疗的潜力。我们在这里显示,SoxE转录因子(包含Sox8、9和10)从出生后脑室下区域(SVZ)早期以自主方式诱导多能神经前体细胞(NPC)成为OPC。我们进行了基于染色质免疫沉淀的生物信息学筛选,并将融合抑制因子(Sufu)鉴定为Sox10抑制的直接靶标。在体外,Sufu的过表达会阻止OPC的产生,而RNAi介导的抑制作用会增加OPC的产生。此外,Sufu杂合子小鼠在发育过程中端脑中OPC的数量增加。我们得出结论,Sox10的作用部分是通过调节Sufu的表达来限制NPC向少突胶质细胞谱系的潜能。

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