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神经调节蛋白诱导小脑颗粒细胞中GABA(A)受体亚基表达及神经突生长。

Neuregulin induces GABA(A) receptor subunit expression and neurite outgrowth in cerebellar granule cells.

作者信息

Rieff H I, Raetzman L T, Sapp D W, Yeh H H, Siegel R E, Corfas G

机构信息

Division of Neuroscience, Department of Neurology, Children's Hospital and Harvard Medical School, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Neurosci. 1999 Dec 15;19(24):10757-66. doi: 10.1523/JNEUROSCI.19-24-10757.1999.

Abstract

Neuregulin (NRG), a growth and differentiation factor that signals via erbB receptor tyrosine kinases, has been shown to have biological effects in both the CNS and the peripheral nervous system. We report here that erbB4 is expressed in mature cerebellar granule cells, where it appears to be concentrated at the granule cell postsynaptic terminals. We also show that one form of NRG, Ig-NRG, plays a crucial role in aspects of cerebellar granule cell development in vitro. First, Ig-NRG treatment of granule cells in culture selectively induces the expression of the GABA(A) receptor beta2 subunit. This increase in subunit expression is paralleled by an increase in functional GABA(A) receptors. In contrast to its effects on GABA(A) receptor subunit expression, Ig-NRG does not upregulate NMDA receptor N2B and N2C subunit expression. Second, we demonstrate that Ig-NRG also enhances neurite outgrowth from cultured granule cells. Ig-NRG does not, however, act as a survival factor for the granule cells. We have compared the effect of Ig-NRG with the effects of brain-derived neurotrophic factor (BDNF), a neurotrophin that exerts specific effects on granule cells in culture, and found that BDNF does not mimic the effects of Ig-NRG on GABA(A) receptor subunit expression. Our results show that Ig-NRG has specific effects on granule cell development and maturation and may regulate these processes in vivo.

摘要

神经调节蛋白(NRG)是一种通过erbB受体酪氨酸激酶发出信号的生长和分化因子,已被证明在中枢神经系统和外周神经系统中均具有生物学效应。我们在此报告,erbB4在成熟的小脑颗粒细胞中表达,它似乎集中在颗粒细胞的突触后终末。我们还表明,NRG的一种形式,即Ig-NRG,在体外小脑颗粒细胞发育的多个方面起着关键作用。首先,用Ig-NRG处理培养中的颗粒细胞可选择性诱导GABA(A)受体β2亚基的表达。亚基表达的这种增加与功能性GABA(A)受体的增加平行。与它对GABA(A)受体亚基表达的影响相反,Ig-NRG不会上调NMDA受体N2B和N2C亚基的表达。其次,我们证明Ig-NRG还能增强培养的颗粒细胞的神经突生长。然而,Ig-NRG并非颗粒细胞的存活因子。我们将Ig-NRG的作用与脑源性神经营养因子(BDNF)的作用进行了比较,BDNF是一种对培养中的颗粒细胞发挥特定作用的神经营养因子,结果发现BDNF不会模拟Ig-NRG对GABA(A)受体亚基表达的影响。我们的结果表明,Ig-NRG对颗粒细胞的发育和成熟具有特定作用,并且可能在体内调节这些过程。

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