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CLC-2 是少突胶质前体细胞分化和髓鞘形成的正向调节剂。

CLC-2 is a positive modulator of oligodendrocyte precursor cell differentiation and myelination.

机构信息

Department of Neurology, General Hospital of Ningxia Medical University, Yinchuan, Ningxia 750004, P.R. China.

Ningxia Key Laboratory of Cerebrocranial Diseases, Basic Medical School of Ningxia Medical University, Yinchuan, Ningxia 750004, P.R. China.

出版信息

Mol Med Rep. 2018 Mar;17(3):4515-4523. doi: 10.3892/mmr.2018.8439. Epub 2018 Jan 17.

Abstract

Oligodendrocytes (OLs) are myelin-forming cells that are present within the central nervous system. Impaired oligodendrocyte precursor cell (OPC) differentiation into mature OLs is a major cause of demyelination diseases. Therefore, identifying the underlying molecular mechanisms of OPC differentiation is crucial to understand the processes of myelination and demyelination. It has been acknowledged that various extrinsic and intrinsic factors are involved in the control of OPC differentiation; however, the function of ion channels, particularly the voltage‑gated chloride channel (CLC), in OPC differentiation and myelination are not fully understood. The present study demonstrated that CLC‑2 may be a positive modulator of OPC differentiation and myelination. Western blotting results revealed that CLC‑2 was expressed in both OPCs and OLs. Furthermore, CLC‑2 currents (ICLC‑2) were recorded in both types of cells. The inhibition of ICLC‑2 by GaTx2, a blocker of CLC‑2, was demonstrated to be higher in OPCs compared with OLs, indicating that CLC‑2 may serve a role in OL differentiation. The results of western blotting and immunofluorescence staining also demonstrated that the expression levels of myelin basic protein were reduced following GaTx2 treatment, indicating that the differentiation of OPCs into OLs was inhibited following CLC‑2 inhibition. In addition, following western blot analysis, it was also demonstrated that the protein expression of the myelin proteins yin yang 1, myelin regulatory factor, Smad‑interacting protein 1 and sex‑determining region Y‑box 10 were regulated by CLC‑2 inhibition. Taken together, the results of the present study indicate that CLC‑2 may be a positive regulator of OPC differentiation and able to contribute to myelin formation and repair in myelin‑associated diseases by controlling the number and open state of CLC-2 channels.

摘要

少突胶质细胞(OLs)是中枢神经系统中形成髓鞘的细胞。少突胶质前体细胞(OPC)分化为成熟 OLs 的能力受损是脱髓鞘疾病的主要原因。因此,确定 OPC 分化的潜在分子机制对于理解髓鞘形成和脱髓鞘过程至关重要。已经认识到,各种外在和内在因素参与了 OPC 分化的控制;然而,离子通道,特别是电压门控氯离子通道(CLC),在 OPC 分化和髓鞘形成中的作用尚未完全阐明。本研究表明,CLC-2 可能是 OPC 分化和髓鞘形成的正向调节剂。Western blot 结果显示,CLC-2 在 OPC 和 OL 中均有表达。此外,在这两种细胞中均记录到 CLC-2 电流(ICLC-2)。CLC-2 的抑制剂 GaTx2 在 OPC 中的抑制作用高于 OL,表明 CLC-2 可能在 OL 分化中发挥作用。Western blot 和免疫荧光染色的结果也表明,GaTx2 处理后髓鞘碱性蛋白的表达水平降低,表明 CLC-2 抑制后 OPC 向 OL 的分化受到抑制。此外,Western blot 分析后还表明,CLC-2 抑制调节了髓鞘蛋白 yin yang 1、髓鞘调节因子、Smad 相互作用蛋白 1 和性别决定区 Y 盒 10 的蛋白表达。综上所述,本研究结果表明,CLC-2 可能是 OPC 分化的正向调节剂,通过控制 CLC-2 通道的数量和开放状态,有助于髓鞘相关疾病中的髓鞘形成和修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7db/5802228/9936e64b8c8c/MMR-17-03-4515-g00.jpg

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