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施万细胞通过转录因子 Sox10 形成郎飞结。

Formation of the node of Ranvier by Schwann cells is under control of transcription factor Sox10.

机构信息

Institut für Biochemie, Emil-Fischer-Zentrum, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

Zahnklinik 3 - Kieferorthopädie, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

出版信息

Glia. 2021 Jun;69(6):1464-1477. doi: 10.1002/glia.23973. Epub 2021 Feb 10.

DOI:10.1002/glia.23973
PMID:33566433
Abstract

The transcription factor Sox10 is an essential regulator of genes that code for structural components of the myelin sheath and for lipid metabolic enzymes in both types of myelinating glia in the central and peripheral nervous systems. In an attempt to characterize additional Sox10 target genes in Schwann cells, we identified in this study a strong influence of Sox10 on the expression of genes associated with adhesion in the MSC80 Schwann cell line. These included the genes for Gliomedin, Neuronal cell adhesion molecule and Neurofascin that together constitute essential Schwann cell contributions to paranode and node of Ranvier. Using bioinformatics and molecular biology techniques we provide evidence that Sox10 directly activates these genes by binding to conserved regulatory regions. For activation, Sox10 cooperates with Krox20, a transcription factor previously identified as the central regulator of Schwann cell myelination. Both the activating function of Sox10 as well as its cooperation with Krox20 were confirmed in vivo. We conclude that the employment of Sox10 and Krox20 as regulators of structural myelin sheath components and genes associated with the node of Ranvier is one way of ensuring a biologically meaningful coordinated formation of both structures during peripheral myelination.

摘要

转录因子 Sox10 是髓鞘结构成分编码基因和中枢及周围神经系统中两种髓鞘形成胶质细胞中脂质代谢酶编码基因的重要调节因子。为了鉴定 Schwann 细胞中 Sox10 的其他靶基因,我们在本研究中发现 Sox10 对 MSC80 Schwann 细胞系中与黏附相关基因的表达有很强的影响。这些基因包括 Gliomedin、神经细胞黏附分子和神经束蛋白,它们共同构成了髓鞘形成细胞参与结间体和郎飞结的必需成分。我们利用生物信息学和分子生物学技术提供了证据,证明 Sox10 通过结合保守的调控区直接激活这些基因。为了激活,Sox10 与 Krox20 合作,Krox20 是先前被鉴定为 Schwann 细胞髓鞘形成中枢调节因子的转录因子。Sox10 的激活功能及其与 Krox20 的合作在体内都得到了证实。我们得出结论,Sox10 和 Krox20 作为髓鞘结构成分和与郎飞结相关基因的调节因子的使用是确保外周髓鞘形成过程中这两种结构具有生物学意义的协调形成的一种方式。

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