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神经营养素前体、癫痫发作和神经元凋亡。

Proneurotrophins, seizures, and neuronal apoptosis.

机构信息

Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA.

出版信息

Neuroscientist. 2010 Jun;16(3):244-52. doi: 10.1177/1073858409349903. Epub 2010 Apr 1.

Abstract

Neurons respond to numerous factors in their environment that influence their survival and function during development and in the mature brain. Among these factors, the neurotrophins have been shown to support neuronal survival and function, acting primarily through the Trk family of receptor tyrosine kinases. However, recent studies have established that the uncleaved neurotrophin precursors, the proneurotrophins, can be secreted and induce apoptosis via the p75 neurotrophin receptor, suggesting that the balance of secreted mature and proneurotrophins has a critical impact on neuronal survival or death. Epileptic seizures elicit increases in both proneurotrophin secretion and p75(NTR) expression, shifting the balance of these factors toward signaling cell death. This review will discuss the evidence that this ligand-receptor system plays an important role in neuronal loss following seizures.

摘要

神经元会对其环境中的多种因素做出反应,这些因素会影响它们在发育过程中和成熟大脑中的存活和功能。在这些因素中,神经营养因子已被证明可以支持神经元的存活和功能,主要通过受体酪氨酸激酶家族的 Trk 发挥作用。然而,最近的研究已经确定,未切割的神经营养因子前体,即前神经生长因子,可以被分泌出来,并通过 p75 神经营养因子受体诱导细胞凋亡,这表明分泌的成熟和前神经生长因子的平衡对神经元的存活或死亡有至关重要的影响。癫痫发作会引起前神经生长因子分泌和 p75(NTR)表达增加,从而使这些因素的平衡向信号传递细胞死亡的方向倾斜。这篇综述将讨论这一配体-受体系统在癫痫发作后神经元丢失中发挥重要作用的证据。

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