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在经历沃勒变性的神经的雪旺细胞中,黏附和增殖在体外增强。

Adhesion and proliferation are enhanced in vitro in Schwann cells from nerve undergoing Wallerian degeneration.

作者信息

Komiyama A, Novicki D L, Suzuki K

机构信息

Department of Pathology, School of Medicine, University of North Carolina, Chapel Hill 27599-7525.

出版信息

J Neurosci Res. 1991 Jul;29(3):308-18. doi: 10.1002/jnr.490290306.

Abstract

Proliferation of Schwann cells during nerve degeneration or regeneration is well documented in vivo. We investigated whether the proliferative response of Schwann cells to injury is retained in vitro. Using 5-month-old male C57BL mice, Schwann cells were isolated from sciatic nerves under 3 experimental conditions: (1) uninjured, (2) after permanent nerve-transection, or (3) after nerve-crush, which permits axonal regeneration. Schwann cells rarely attached to polylysine-coated coverslips when isolated from uninjured or 1 day posttransection/crush nerves. The number of adherent cells increased when Schwann cells were isolated 3 days after nerve-transection or -crush. When cells were isolated from transected nerves, cell adhesion reached a peak 2 weeks after the injury and then declined. Maximal attachment of Schwann cells occurred when the cells were isolated 2-4 weeks after nerve-crush. The percentage of Schwann cells with spreading processes corresponded closely with the number of thymidine-labeled cells at 1 day in vitro. The in vitro capacity of cells to spread and incorporate thymidine reached maximal levels at 5 days posttransection/crush. Capacity of cells to spread and incorporate thymidine subsequently decreased with time following transection. However, a biphasic elevation in cell spreading and thymidine incorporation was observed in Schwann cells isolated from crushed nerves. Maximal growth of Schwann cells in vitro occurred at 1-2 weeks posttransection and at 1-4 weeks postcrush. Adhesion and spreading of Schwann cells were promoted by coating coverslips with laminin or fibronectin. Preincubation of Schwann cells with soluble laminin or fibronectin prevented the initial cell attachment induced by the corresponding protein. Our results suggest that Schwann cells from injured nerves possess binding sites for laminin and fibronectin, which are, in part, responsible for the enhanced adhesion of Schwann cells in vitro. This study provides a new method for preparation of Schwann cells from peripheral nerves of adult mice.

摘要

雪旺细胞在神经退变或再生过程中的增殖在体内已有充分记录。我们研究了雪旺细胞对损伤的增殖反应在体外是否得以保留。使用5月龄雄性C57BL小鼠,在3种实验条件下从坐骨神经中分离雪旺细胞:(1) 未损伤,(2) 永久性神经横断后,或(3) 神经挤压后,后者允许轴突再生。从未损伤或横断/挤压神经1天后分离的雪旺细胞很少附着于聚赖氨酸包被的盖玻片。当在神经横断或挤压3天后分离雪旺细胞时,贴壁细胞数量增加。当从横断神经中分离细胞时,细胞黏附在损伤后2周达到峰值,然后下降。当在神经挤压后2 - 4周分离细胞时,雪旺细胞的附着达到最大值。具有伸展突起的雪旺细胞百分比与体外1天时胸苷标记细胞数量密切相关。细胞伸展和掺入胸苷的体外能力在横断/挤压后5天达到最高水平。横断后,细胞伸展和掺入胸苷的能力随后随时间下降。然而,在从挤压神经中分离的雪旺细胞中观察到细胞伸展和胸苷掺入呈双相升高。雪旺细胞在体外的最大生长发生在横断后1 - 2周和挤压后1 - 4周。用层粘连蛋白或纤连蛋白包被盖玻片可促进雪旺细胞的黏附和伸展。用可溶性层粘连蛋白或纤连蛋白对雪旺细胞进行预孵育可阻止相应蛋白质诱导的初始细胞附着。我们的结果表明,来自损伤神经的雪旺细胞具有层粘连蛋白和纤连蛋白的结合位点,这在一定程度上负责雪旺细胞在体外的增强黏附。本研究提供了一种从成年小鼠外周神经制备雪旺细胞的新方法。

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