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

机译:神经营养蛋白受体对胆碱能基底前脑发育连通性和功能的调节

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摘要

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.
机译:胆碱能基底前脑(cBF)神经元除表达胆碱能标记外,还通过表达p75神经营养蛋白受体(p75)和原肌球蛋白相关激酶(Trk)神经营养蛋白受体来定义。已知神经营养蛋白,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,尽管在痴呆症中,营养信号减少,并且p75介导cBF神经元的神经变性,但神经营养蛋白信号在调节成人cBF功能中的作用尚不清楚。在这里,我们回顾了当前对cBF神经元是如何被激活p75和TrkA,B或C的神经营养蛋白调节的,以影响这些神经元在正常皮层功能中发挥的关键作用,特别是高阶认知。具体来说,我们描述了神经营养蛋白调节基底前脑神经元发育及其在维持和修饰成熟的基底前脑突触和皮质微电路连通性中的作用的当前证据。理解神经营养蛋白信号在调节胆碱能连通性的精确性中的作用将有助于对正常认知过程的理解,并且可能为设计改进的治疗已证明胆碱能功能障碍的神经系统疾病的疗法提供其他思路。

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