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脑源性神经营养因子/丝裂原活化蛋白激酶/细胞外信号调节激酶诱导发育中的大脑皮质中的骨形态发生蛋白 7 表达诱导过早的放射状胶质细胞分化,并损害神经元迁移。

BDNF/MAPK/ERK-induced BMP7 expression in the developing cerebral cortex induces premature radial glia differentiation and impairs neuronal migration.

机构信息

Unit of Cell Biology, Department of Experimental Pathology and Therapeutics, School of Medicine, University of Barcelona, 08907 L'Hospitalet de Llobregat, Spain.

出版信息

Cereb Cortex. 2010 Sep;20(9):2132-44. doi: 10.1093/cercor/bhp275. Epub 2009 Dec 27.

Abstract

During development of the mammalian nervous system, a combination of genetic and environmental factors governs the sequential generation of neurons and glia and the initial establishment of the neural circuitry. Here, we demonstrate that brain-derived neurotrophic factor (BDNF), one of those local acting factors, induces Bone Morphogenetic Protein 7 (BMP7) expression in embryonic neurons by activating Mitogen-Activated Protein Kinase/Extracellular signal-Regulated Kinase signaling and by the negative regulation of p53/p73 function. We also show that intraventricular injection of BMP7 at midgestation induces the early differentiation of radial glia into glial precursors and astrocytes and the expression of mature glial markers such as the antiadhesive protein SC1. As a result of this precocious radial glia maturation, the laminar distribution of late-born pyramidal neurons is altered, most likely by the termination of radial glia ability to support neuronal migration and the early neuronal detachment from the glial rail. We propose a mechanism for BDNF regulation of BMP7 in which local activity-driven BDNF-induced BMP7 expression at the end of neurogenesis instructs competent precursors to generate astrocytes. Such a mechanism might ensure synchronic neuronal and glial maturation at the beginning of cortical activity.

摘要

在哺乳动物神经系统的发育过程中,遗传和环境因素的结合决定了神经元和神经胶质的顺序产生以及神经回路的初步建立。在这里,我们证明了脑源性神经营养因子(BDNF),作为局部作用因子之一,通过激活丝裂原活化蛋白激酶/细胞外信号调节激酶信号通路和负调控 p53/p73 功能,诱导胚胎神经元中骨形成蛋白 7(BMP7)的表达。我们还表明,在妊娠中期向脑室中注射 BMP7 会诱导放射状胶质早期分化为神经前体细胞和星形胶质细胞,并表达成熟的神经胶质标志物,如抗粘连蛋白 SC1。由于这种早熟的放射状胶质成熟,出生较晚的锥体神经元的层状分布发生改变,很可能是由于放射状胶质支持神经元迁移的能力终止以及神经元过早脱离胶质轨道。我们提出了 BDNF 调节 BMP7 的一种机制,即在神经发生末期,局部活性驱动的 BDNF 诱导 BMP7 表达,从而指导成熟的前体细胞产生星形胶质细胞。这种机制可能确保皮质活动开始时神经元和神经胶质同步成熟。

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