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尿激酶型纤溶酶原激活物-尿激酶型纤溶酶原激活物受体分子复合物在神经元迁移和神经突形成过程中参与细胞信号传导。

uPA-uPAR molecular complex is involved in cell signaling during neuronal migration and neuritogenesis.

作者信息

Lino Noelia, Fiore Luciano, Rapacioli Melina, Teruel Luisa, Flores Vladimir, Scicolone Gabriel, Sánchez Viviana

机构信息

Laboratory of Developmental Neurobiology, Institute of Cell Biology and Neurosciences "Prof. E. De Robertis" (UBA-CONICET), School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.

出版信息

Dev Dyn. 2014 May;243(5):676-89. doi: 10.1002/dvdy.24114. Epub 2014 Feb 19.

Abstract

BACKGROUND

In the development of the central nervous system (CNS), neuronal migration and neuritogenesis are crucial processes for establishing functional neural circuits. This relies on the regulation exerted by several signaling molecules, which play important roles in axonal growth and guidance. The urokinase-type plasminogen activator (uPA)-in association with its receptor-triggers extracellular matrix proteolysis and other cellular processes through the activation of intracellular signaling pathways. Even though the uPA-uPAR complex is well characterized in nonneuronal systems, little is known about its signaling role during CNS development.

RESULTS

In response to uPA, neuronal migration and neuritogenesis are promoted in a dose-dependent manner. After stimulation, uPAR interacts with α5- and β1-integrin subunits, which may constitute an αβ-heterodimer that acts as a uPA-uPAR coreceptor favoring the activation of multiple kinases. This interaction may be responsible for the uPA-promoted phosphorylation of focal adhesion kinase (FAK) and its relocation toward growth cones, triggering cytoskeletal reorganization which, in turn, induces morphological changes related to neuronal migration and neuritogenesis.

CONCLUSIONS

uPA has a key role during CNS development. In association with its receptor, it orchestrates both proteolytic and nonproteolytic events that govern the proper formation of neural networks.

摘要

背景

在中枢神经系统(CNS)的发育过程中,神经元迁移和神经突发生是建立功能性神经回路的关键过程。这依赖于几种信号分子所发挥的调节作用,这些信号分子在轴突生长和导向中起着重要作用。尿激酶型纤溶酶原激活剂(uPA)与其受体相结合,通过激活细胞内信号通路触发细胞外基质蛋白水解及其他细胞过程。尽管uPA - uPAR复合物在非神经元系统中已得到充分表征,但关于其在CNS发育过程中的信号传导作用却知之甚少。

结果

响应uPA,神经元迁移和神经突发生以剂量依赖性方式得到促进。刺激后,uPAR与α5和β1整合素亚基相互作用,这可能构成一个αβ异二聚体,作为uPA - uPAR共受体,有利于多种激酶的激活。这种相互作用可能是uPA促进粘着斑激酶(FAK)磷酸化及其向生长锥重新定位的原因,从而触发细胞骨架重组,进而诱导与神经元迁移和神经突发生相关的形态变化。

结论

uPA在CNS发育过程中起关键作用。与其受体相结合,它协调了蛋白水解和非蛋白水解事件,这些事件控制着神经网络的正常形成。

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