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BAI黏附型G蛋白偶联受体在突触发育和可塑性中的新作用

Emerging Roles of BAI Adhesion-GPCRs in Synapse Development and Plasticity.

作者信息

Duman Joseph G, Tu Yen-Kuei, Tolias Kimberley F

机构信息

Department of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

Department of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA; Integrative Molecular and Biomedical Sciences Program, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

出版信息

Neural Plast. 2016;2016:8301737. doi: 10.1155/2016/8301737. Epub 2016 Jan 4.

Abstract

Synapses mediate communication between neurons and enable the brain to change in response to experience, which is essential for learning and memory. The sites of most excitatory synapses in the brain, dendritic spines, undergo rapid remodeling that is important for neural circuit formation and synaptic plasticity. Abnormalities in synapse and spine formation and plasticity are associated with a broad range of brain disorders, including intellectual disabilities, autism spectrum disorders (ASD), and schizophrenia. Thus, elucidating the mechanisms that regulate these neuronal processes is critical for understanding brain function and disease. The brain-specific angiogenesis inhibitor (BAI) subfamily of adhesion G-protein-coupled receptors (adhesion-GPCRs) has recently emerged as central regulators of synapse development and plasticity. In this review, we will summarize the current knowledge regarding the roles of BAIs at synapses, highlighting their regulation, downstream signaling, and physiological functions, while noting the roles of other adhesion-GPCRs at synapses. We will also discuss the relevance of BAIs in various neurological and psychiatric disorders and consider their potential importance as pharmacological targets in the treatment of these diseases.

摘要

突触介导神经元之间的通讯,并使大脑能够根据经验发生变化,这对学习和记忆至关重要。大脑中大多数兴奋性突触的部位,即树突棘,会经历快速重塑,这对神经回路形成和突触可塑性很重要。突触和树突棘形成及可塑性的异常与多种脑部疾病相关,包括智力残疾、自闭症谱系障碍(ASD)和精神分裂症。因此,阐明调节这些神经元过程的机制对于理解脑功能和疾病至关重要。粘附性G蛋白偶联受体(adhesion-GPCRs)的脑特异性血管生成抑制因子(BAI)亚家族最近已成为突触发育和可塑性的核心调节因子。在本综述中,我们将总结关于BAI在突触中的作用的当前知识,强调其调节、下游信号传导和生理功能,同时指出其他粘附性GPCRs在突触中的作用。我们还将讨论BAI在各种神经和精神疾病中的相关性,并考虑它们作为治疗这些疾病的药理学靶点的潜在重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ad/4736325/bfe3f349d154/NP2016-8301737.001.jpg

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