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微管相关蛋白1B的两种磷酸化模式在周围神经再生过程中受到不同调控。

Two modes of microtubule-associated protein 1B phosphorylation are differentially regulated during peripheral nerve regeneration.

作者信息

Ramón-Cueto A, Avila J

机构信息

Centro de Biología Molecular 'Severo Ochoa' (CSIC-UAM), Facultad de Ciencias, Universidad Autónoma de Madrid, Spain.

出版信息

Brain Res. 1999 Jan 9;815(2):213-26. doi: 10.1016/s0006-8993(98)01092-0.

Abstract

Two major modes of MAP1B phosphorylation (I and II), respectively recognized by monoclonal antibodies 150 and 125, have been related to remodeling and formation of processes in the mature nervous system. To gain insight into the cytoskeletal modifications underlying peripheral nerve regeneration, the pattern of expression of both MAP1B phosphorylated modes was studied during this process. Sciatic nerves from adult Wistar rats were crushed and animals allowed to survive for 5, 7, 10 or 14 days. After those survival periods, damaged and undamaged sciatic nerves, dorsal root ganglia (DRG), and spinal cords, were subjected to immunohistochemistry and Western blot, using antibodies 150 and 125. At all survival periods analysed, MAP1B phosphorylated at mode I was concentrated at the distal region of regenerating nerves whereas mode II phosphorylation underwent an overall decrease in regenerating axons that was less evident in more proximal nerve regions. Very high levels of MAP1B phosphorylated at mode II were detected in the bodies of DRG neurons and in bodies and dendrites of spinal motor neurons. This phosphorylation mode was also encountered in some Schwann cells and oligodendroglia associated with more proximal regions of regenerating axons. In this study we conclude that MAP1B was differentially phosphorylated depending on the cell type, subcellular compartment and stage of the regenerative process and discuss the possible functional implications that differential expression of each MAP1B phosphorylation mode might have during nerve regeneration.

摘要

分别由单克隆抗体150和125识别的微管相关蛋白1B(MAP1B)磷酸化的两种主要模式,已被证实与成熟神经系统中突起的重塑和形成有关。为了深入了解外周神经再生过程中潜在的细胞骨架修饰,我们研究了在此过程中两种MAP1B磷酸化模式的表达模式。将成年Wistar大鼠的坐骨神经切断,让动物存活5、7、10或14天。在这些存活期后,使用抗体150和125对受损和未受损的坐骨神经、背根神经节(DRG)和脊髓进行免疫组织化学和蛋白质印迹分析。在所有分析的存活期,模式I磷酸化的MAP1B集中在再生神经的远端区域,而模式II磷酸化在再生轴突中总体减少,在更近端的神经区域不太明显。在DRG神经元的胞体以及脊髓运动神经元的胞体和树突中检测到非常高水平的模式II磷酸化的MAP1B。在一些与再生轴突更近端区域相关的雪旺细胞和少突胶质细胞中也发现了这种磷酸化模式。在本研究中,我们得出结论,MAP1B根据细胞类型、亚细胞区室和再生过程的阶段而发生差异磷酸化,并讨论了每种MAP1B磷酸化模式的差异表达在神经再生过程中可能具有的潜在功能意义。

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