非神经元对突触功能的贡献。

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Ritchy Hodebourg, Michael D Scofield, Peter W Kalivas, Brittany N Kuhn
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引用次数: 0

摘要

突触是完美整合的信号中枢,包含典型的突触元素、神经元突触前和突触后,以及神经细胞的其他成分,包括突触周围星形胶质细胞和细胞外基质蛋白,以及小胶质细胞和少突胶质细胞。这些多部中枢的信号传导对突触功能至关重要,在神经精神疾病中经常被破坏。我们回顾了一些数据,这些数据完善了我们对环境刺激如何塑造突触内的信号和突触可塑性的理解。我们提出的工作模型整合了已知的突触周围神经细胞类型如何调节由成瘾药物引起的突触功能和功能障碍。虽然这些工作模型集成了现有的发现,但它们受到对新技术的需求的限制。因此,我们提出了改进试剂和实验方法的方向,以更好地探索突触周围生态系统中细胞类型之间的信号传导如何创造突触可塑性,从而建立和维持适应和不适应行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nonneuronal contributions to synaptic function.

Synapses are elegantly integrated signaling hubs containing the canonical synaptic elements, neuronal pre- and postsynapses, along with other components of the neuropil, including perisynaptic astroglia and extracellular matrix proteins, as well as microglia and oligodendrocytes. Signaling within these multipartite hubs is essential for synaptic function and is often disrupted in neuropsychiatric disorders. We review data that have refined our understanding of how environmental stimuli shape signaling and synaptic plasticity within synapses. We propose working models that integrate what is known about how different cell types within the perisynaptic neuropil regulate synaptic functions and dysfunctions that are elicited by addictive drugs. While these working models integrate existing findings, they are constrained by a need for new technology. Accordingly, we propose directions for improving reagents and experimental approaches to better probe how signaling between cell types within perisynaptic ecosystems creates the synaptic plasticity necessary to establish and maintain adaptive and maladaptive behaviors.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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