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抑制性突触可塑性的来龙去脉:神经元类型、分子机制和功能作用。

The ins and outs of inhibitory synaptic plasticity: Neuron types, molecular mechanisms and functional roles.

机构信息

Department of Biomedicine, Danish National Research Foundation Center of Excellence PROMEMO, Aarhus University, Aarhus, Denmark.

Dominck P Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

Eur J Neurosci. 2021 Oct;54(8):6882-6901. doi: 10.1111/ejn.14907. Epub 2020 Aug 9.

Abstract

GABAergic interneurons are highly diverse, and their synaptic outputs express various forms of plasticity. Compelling evidence indicates that activity-dependent changes of inhibitory synaptic transmission play a significant role in regulating neural circuits critically involved in learning and memory and circuit refinement. Here, we provide an updated overview of inhibitory synaptic plasticity with a focus on the hippocampus and neocortex. To illustrate the diversity of inhibitory interneurons, we discuss the case of two highly divergent interneuron types, parvalbumin-expressing basket cells and neurogliaform cells, which support unique roles on circuit dynamics. We also present recent progress on the molecular mechanisms underlying long-term, activity-dependent plasticity of fast inhibitory transmission. Lastly, we discuss the role of inhibitory synaptic plasticity in neuronal circuits' function. The emerging picture is that inhibitory synaptic transmission in the CNS is extremely diverse, undergoes various mechanistically distinct forms of plasticity and contributes to a much more refined computational role than initially thought. Both the remarkable diversity of inhibitory interneurons and the various forms of plasticity expressed by GABAergic synapses provide an amazingly rich inhibitory repertoire that is central to a variety of complex neural circuit functions, including memory.

摘要

GABA 能中间神经元具有高度多样性,其突触输出表现出各种形式的可塑性。有强有力的证据表明,抑制性突触传递的活动依赖性变化在调节学习和记忆以及回路细化中起关键作用的神经回路中起着重要作用。在这里,我们提供了一个关于抑制性突触可塑性的最新概述,重点是海马体和新皮层。为了说明抑制性中间神经元的多样性,我们讨论了两种高度不同的中间神经元类型的情况,即表达囊泡蛋白的篮状细胞和神经胶质细胞,它们支持独特的回路动力学作用。我们还介绍了快速抑制性传递的长时程、活动依赖性可塑性的分子机制的最新进展。最后,我们讨论了抑制性突触可塑性在神经元回路功能中的作用。新兴的观点是,中枢神经系统中的抑制性突触传递是极其多样的,经历了各种机制上不同的可塑性形式,并为比最初想象的更为精细的计算作用做出了贡献。抑制性中间神经元的显著多样性和 GABA 能突触表达的各种形式的可塑性为各种复杂的神经回路功能提供了令人惊讶的丰富的抑制性储备,包括记忆。

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