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ProBDNF inhibits collective migration and chemotaxis of rat Schwann cells

机译:ProBDNF抑制大鼠雪旺细胞的集体迁移和趋化性

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Schwann cell migration, including collective migration and chemotaxis, is essential for the formation of coordinate interactions between Schwann cells and axons during peripheral nerve development and regeneration. Moreover, limited migration of Schwann cells imposed a serious obstacle on Schwann cell-astrocytes intermingling and spinal cord repair after Schwann cell transplantation into injured spinal cords. Recent studies have shown that mature brain-derived neurotrophic factor, a member of the neurotrophin family, inhibits Schwann cell migration. The precursor form of brain-derived neurotrophic factor, proBDNF, was expressed in the developing or degenerating peripheral nerves and the injured spinal cords. Since "the yin and yang of neurotrophin action" has been established as a common sense, proBDNF would be expected to promote Schwann cell migration. However, we found, in the present study, that exogenous proBDNF also inhibited in vitro collective migration and chemotaxis of RSC 96 cells, a spontaneously immortalized rat Schwann cell line. Moreover, proBDNF suppressed adhesion and spreading of those cells. At molecular level, proBDNF inhibits F-actin polymerization and focal adhesion dynamics in cultured RSC 96 cells. Therefore, our results suggested a special case against the classical opinion of "the yin and yang of neurotrophin action" and implied that proBDNF might modulate peripheral nerve development or regeneration and spinal cord repair through perturbing native or transplanted Schwann cell migration. (C) 2016 Elsevier Ltd. All rights reserved.
机译:雪旺细胞迁移(包括集体迁移和趋化性)对于在周围神经发育和再生过程中雪旺细胞与轴突之间形成协调相互作用至关重要。此外,雪旺氏细胞的有限迁移对雪旺氏细胞-星状细胞的混合和脊髓损伤修复后的施旺旺细胞-星形胶质细胞混合和脊髓修复构成了严重的障碍。最近的研究表明,成熟的脑源性神经营养因子(神经营养蛋白家族的成员)抑制雪旺细胞的迁移。脑源性神经营养因子proBDNF的前体形式在发育中的或退化的周围神经和受损的脊髓中表达。由于“神经营养蛋白作用的阴阳”已被确定为常识,因此proBDNF有望促进雪旺细胞的迁移。然而,在本研究中,我们发现外源性proBDNF也抑制RSC 96细胞(一种自发永生的大鼠雪旺氏细胞系)的体外集体迁移和趋化性。此外,proBDNF抑制了那些细胞的粘附和扩散。在分子水平上,proBDNF抑制培养的RSC 96细胞中的F-肌动蛋白聚合和粘着动力学。因此,我们的研究结果提出了反对“神经营养蛋白作用的阴阳”经典观点的特例,并暗示proBDNF可能通过干扰天然或移植的施旺细胞迁移来调节周围神经的发育或再生以及脊髓修复。 (C)2016 Elsevier Ltd.保留所有权利。

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