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哺乳类神经系统中 GABA 能和甘氨酸能回路的组装和维护。

Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system.

机构信息

Department of Biological Structure, University of Washington, Seattle, WA, USA.

Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI, USA.

出版信息

Neural Dev. 2018 Jun 7;13(1):12. doi: 10.1186/s13064-018-0109-6.

DOI:10.1186/s13064-018-0109-6
PMID:29875009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5991458/
Abstract

Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition.

摘要

中枢神经系统 (CNS) 的抑制作用是由两种神经递质介导的:γ-氨基丁酸 (GABA) 和甘氨酸。抑制性突触通常是 GABA 能或甘氨酸能的,尽管也有同时释放这两种神经递质的突触。与兴奋性回路相比,关于调节抑制性回路突触伙伴选择和布线模式的细胞和分子机制,人们知之甚少。然而,最近的工作已经开始填补这一知识空白,更深入地了解 GABA 能和甘氨酸能回路的组装和维持是否依赖于共同或不同的机制。在这里,我们总结并对比了调节突触伙伴选择的发育机制,以及促进 GABA 能和甘氨酸能突触及其各自布线模式形成、细化、成熟和维持的发育机制。我们强调了中枢神经系统的某些部分如何在其抑制性突触中表现出抑制性递质或受体组成类型的发育变化。我们还考虑了一种抑制性连接的发育或维持受到干扰如何影响同一回路中其他抑制性突触类型。对 GABA 能和甘氨酸能输入以及同时释放这两种神经递质的输入的发育和维持的机制理解,可以帮助制定治疗突触抑制障碍的综合治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/7dc3445a5f4e/13064_2018_109_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/b03a458cd842/13064_2018_109_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/654db679a6bc/13064_2018_109_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/28303e7ad259/13064_2018_109_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/426a3a33146f/13064_2018_109_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/7dc3445a5f4e/13064_2018_109_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/b03a458cd842/13064_2018_109_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/654db679a6bc/13064_2018_109_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/28303e7ad259/13064_2018_109_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/426a3a33146f/13064_2018_109_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/5991458/7dc3445a5f4e/13064_2018_109_Fig5_HTML.jpg

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