Molecular mechanisms of synaptogenesis.

IF 2.8 4区 医学 Q2 NEUROSCIENCES
Frontiers in Synaptic Neuroscience Pub Date : 2022-09-13 eCollection Date: 2022-01-01 DOI:10.3389/fnsyn.2022.939793
Cai Qi, Li-Da Luo, Irena Feng, Shaojie Ma
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引用次数: 7

Abstract

Synapses are the basic units for information processing and storage in the nervous system. It is only when the synaptic connection is established, that it becomes meaningful to discuss the structure and function of a circuit. In humans, our unparalleled cognitive abilities are correlated with an increase in the number of synapses. Additionally, genes involved in synaptogenesis are also frequently associated with neurological or psychiatric disorders, suggesting a relationship between synaptogenesis and brain physiology and pathology. Thus, understanding the molecular mechanisms of synaptogenesis is the key to the mystery of circuit assembly and neural computation. Furthermore, it would provide therapeutic insights for the treatment of neurological and psychiatric disorders. Multiple molecular events must be precisely coordinated to generate a synapse. To understand the molecular mechanisms underlying synaptogenesis, we need to know the molecular components of synapses, how these molecular components are held together, and how the molecular networks are refined in response to neural activity to generate new synapses. Thanks to the intensive investigations in this field, our understanding of the process of synaptogenesis has progressed significantly. Here, we will review the molecular mechanisms of synaptogenesis by going over the studies on the identification of molecular components in synapses and their functions in synaptogenesis, how cell adhesion molecules connect these synaptic molecules together, and how neural activity mobilizes these molecules to generate new synapses. Finally, we will summarize the human-specific regulatory mechanisms in synaptogenesis and results from human genetics studies on synaptogenesis and brain disorders.

Abstract Image

Abstract Image

Abstract Image

突触发生的分子机制。
突触是神经系统中处理和储存信息的基本单位。只有建立了突触连接,讨论电路的结构和功能才有意义。在人类中,我们无与伦比的认知能力与突触数量的增加有关。此外,参与突触发生的基因也经常与神经或精神疾病有关,这表明突触发生与脑生理和病理之间存在关系。因此,了解突触发生的分子机制是解开电路组装和神经计算之谜的关键。此外,它将为神经和精神疾病的治疗提供治疗见解。多个分子事件必须精确协调才能产生突触。为了理解突触发生的分子机制,我们需要知道突触的分子成分,这些分子成分是如何结合在一起的,以及分子网络是如何根据神经活动而改进以产生新的突触的。由于在这一领域的深入研究,我们对突触发生过程的理解取得了重大进展。本文将从突触分子成分的鉴定及其在突触发生中的作用、细胞粘附分子如何将突触分子连接在一起、神经活动如何动员这些分子产生新突触等方面对突触发生的分子机制进行综述。最后,我们将总结人类突触发生的特异性调控机制以及人类遗传学在突触发生和脑部疾病方面的研究成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
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