首页> 美国卫生研究院文献>The Journal of Neuroscience >Expression of the Nerve Growth Factor Receptors TrkA and p75NTR in the Visual Cortex of the Rat: Development and Regulation by the Cholinergic Input
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Expression of the Nerve Growth Factor Receptors TrkA and p75NTR in the Visual Cortex of the Rat: Development and Regulation by the Cholinergic Input

机译:神经生长因子受体TrkA和p75NTR在大鼠的视觉皮层的表达:胆碱能输入的发展和调控。

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摘要

Several lines of evidence have shown that nerve growth factor (NGF), the progenitor of the neurotrophin family of growth factors, plays a fundamental role in the developmental plasticity of the rat visual cortex. However, the expression of NGF receptors (NGFRs) TrkA and p75NTR and the possible sites of NGF action in the visual cortex remain to be elucidated so far. Using a highly sensitive ECL immunoblot analysis, we have been able to show, in the present study, that the TrkA protein is expressed in the rat visual cortex and that it is developmentally upregulated during the critical period for cortical plasticity. In contrast, the expression level of the low-affinity NGF receptor p75NTR seems to remain nearly constant throughout development. In the analysis of possible pathways involved in the regulation of NGFR expression, we found that neither blockade of the visual input nor NGF administration to the visual cortex resulted in a modulation of NGFR levels of expression. On the other hand, the selective destruction of cholinergic afferents to the visual cortex caused a dramatic, but not complete, reduction of the cortical NGFRs, which suggests that these receptors are located on cholinergic terminals predominantly. At the functional level, we found that, after the elimination of the cholinergic afferents to the visual cortex, the NGF-induced increase of both acetylcholine and glutamate release from cortical synaptosomes was strongly impaired. These results indicate that the cholinergic input is an important mediator of visual cortex responsiveness to NGF action.
机译:几条证据表明,神经生长因子神经营养蛋白家族的祖细胞神经生长因子(NGF)在大鼠视皮层的发育可塑性中起着基本作用。然而,迄今为止尚不清楚NGF受体TrkA和p75 NTR 的表达以及NGF在视觉皮层中的作用部位。使用高度敏感的ECL免疫印迹分析,我们已经能够显示,在本研究中,TrkA蛋白在大鼠的视皮层中表达,并且在皮层可塑性的关键时期被发育上调。相反,低亲和力NGF受体p75 NTR 的表达水平似乎在整个发育过程中几乎保持恒定。在分析调控NGFR表达的可能途径中,我们发现视觉输入的阻断或NGF对视觉皮层的给药均不会导致NGFR表达水平的调节。另一方面,选择性破坏胆碱能传入视觉皮层会引起皮质NGFR的急剧减少,但并不完全,这表明这些受体主要位于胆碱能末端。在功能水平上,我们发现消除视觉皮层的胆碱能传入后,NGF诱导的乙酰胆碱和谷氨酸从皮质突触小体中释放的增加受到了严重损害。这些结果表明胆碱能输入是视觉皮层对NGF作用的重要介体。

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