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神经营养因子受体对胆碱能基底前脑发育、连接性及功能的调节

Regulation of cholinergic basal forebrain development, connectivity, and function by neurotrophin receptors.

作者信息

Boskovic Zoran, Meier Sonja, Wang Yunpeng, Milne Michael R, Onraet Tessa, Tedoldi Angelo, Coulson Elizabeth J

机构信息

Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, Australia.

Clem Jones Centre for Ageing Dementia Research, The University of Queensland, Brisbane, Queensland, Australia.

出版信息

Neuronal Signal. 2019 Mar;3(1):NS20180066. doi: 10.1042/NS20180066. Epub 2019 Feb 4.

Abstract

Cholinergic basal forebrain (cBF) neurons are defined by their expression of the p75 neurotrophin receptor (p75) and tropomyosin-related kinase (Trk) neurotrophin receptors in addition to cholinergic markers. It is known that the neurotrophins, particularly nerve growth factor (NGF), mediate cholinergic neuronal development and maintenance. However, the role of neurotrophin signalling in regulating adult cBF function is less clear, although in dementia, trophic signalling is reduced and p75 mediates neurodegeneration of cBF neurons. Here we review the current understanding of how cBF neurons are regulated by neurotrophins which activate p75 and TrkA, B or C to influence the critical role that these neurons play in normal cortical function, particularly higher order cognition. Specifically, we describe the current evidence that neurotrophins regulate the development of basal forebrain neurons and their role in maintaining and modifying mature basal forebrain synaptic and cortical microcircuit connectivity. Understanding the role neurotrophin signalling plays in regulating the precision of cholinergic connectivity will contribute to the understanding of normal cognitive processes and will likely provide additional ideas for designing improved therapies for the treatment of neurological disease in which cholinergic dysfunction has been demonstrated.

摘要

胆碱能基底前脑(cBF)神经元除了表达胆碱能标志物外,还通过其对p75神经营养因子受体(p75)和原肌球蛋白相关激酶(Trk)神经营养因子受体的表达来定义。已知神经营养因子,特别是神经生长因子(NGF),介导胆碱能神经元的发育和维持。然而,神经营养因子信号传导在调节成年cBF功能中的作用尚不清楚,尽管在痴呆症中,营养信号传导减少,p75介导cBF神经元的神经变性。在这里,我们综述了目前对cBF神经元如何受神经营养因子调节的理解,这些神经营养因子激活p75和TrkA、B或C,以影响这些神经元在正常皮质功能,特别是高阶认知中所起的关键作用。具体而言,我们描述了目前的证据,即神经营养因子调节基底前脑神经元的发育及其在维持和改变成熟基底前脑突触和皮质微电路连接中的作用。了解神经营养因子信号传导在调节胆碱能连接精确性中的作用,将有助于理解正常认知过程,并可能为设计改善疗法提供更多思路,以治疗已证实存在胆碱能功能障碍的神经疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25b1/7363335/32a654aa089f/ns-03-ns20180066-g1.jpg

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