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迈向对衰老过程中神经元可塑性丧失的分子基础的理解。

Toward understanding of the molecular basis of loss of neuronal plasticity in ageing.

作者信息

Mori N

机构信息

Division of Neurogerontology, Ethel Percy Andrus Gerontology Center, University of Southern California, Los Angeles 90089.

出版信息

Age Ageing. 1993 Jan;22(1):S5-18.

PMID:8438656
Abstract

Although there are several lines of evidence which suggest that neuronal plasticity decreases in some regions of both the central and peripheral nervous systems as well as in neuroendocrine tissues during development and ageing, the molecular mechanisms underlying loss of plasticity are largely unknown. To explore this question, we examined changes in expression profiles of neuronal growth-associated proteins (nGAPs) during ageing as well as the molecular regulatory mechanisms of their induction by nerve growth factor (NGF). SCG10, one of the nGAPs, is expressed in subsets of central neurons which maintain a high degree of plasticity in the adult, and is induced after neuronal deafferentation. This is a basis for analysing if SCG10 is involved in the remodelling of adult neurons during reactive synaptogenesis in diseased brains as well as in normal ageing. Studies of the induction of SCG10 by NGF in PC12 cells suggest that transcriptional inducible element(s) are present, at least in part, in the upstream region of the SCG10 gene. These studies of the regulation of nGAPs in ageing brains and neuroendocrine cells may yield new insights on reactivating neurites of partially degenerated neurons in the ageing brain.

摘要

尽管有几条证据表明,在发育和衰老过程中,中枢神经系统和外周神经系统的某些区域以及神经内分泌组织中的神经元可塑性会降低,但可塑性丧失背后的分子机制在很大程度上尚不清楚。为了探究这个问题,我们研究了在衰老过程中神经元生长相关蛋白(nGAPs)表达谱的变化以及神经生长因子(NGF)对其诱导的分子调控机制。nGAPs之一的SCG10在成年后保持高度可塑性的中枢神经元亚群中表达,并在神经元去传入后被诱导。这是分析SCG10是否参与患病大脑以及正常衰老过程中反应性突触形成期间成年神经元重塑的基础。对PC12细胞中NGF诱导SCG10的研究表明,转录诱导元件至少部分存在于SCG10基因的上游区域。这些对衰老大脑和神经内分泌细胞中nGAPs调控的研究可能会为重新激活衰老大脑中部分退化神经元的神经突提供新的见解。

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