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神经胶质细胞:调节突触可塑性的多种方式。

Glia: the many ways to modulate synaptic plasticity.

机构信息

Ecole Normale Supérieure, INSERM U789, Paris, France.

出版信息

Neurochem Int. 2010 Nov;57(4):440-5. doi: 10.1016/j.neuint.2010.02.013. Epub 2010 Mar 1.

Abstract

Synaptic plasticity consists in a change in synaptic strength that is believed to be the basis of learning and memory. Synaptic plasticity has been for a very long period of time a hallmark of neurons. Recent advances in physiology of glial cells indicate that astrocyte and microglia possess all the features to participate and modulate the various form of synaptic plasticity. Indeed beside their respective supportive and immune functions an increasing number of study demonstrate that astrocytes and microglia express receptors for most neurotransmitters and release neuroactive substances that have been shown to modulate neuronal activity and synaptic plasticity. Because glial cells are all around synapses and release a wide variety of neuroactive molecule during physiological and pathological conditions, glial cells have been reported to modulate synaptic plasticity in many different ways. From change in synaptic coverage, to release of chemokines and cytokines up to dedicated "glio" transmitters release, glia were reported to affect synaptic scaling, homeostatic plasticity, metaplasticity, long-term potentiation and long-term depression.

摘要

突触可塑性是指突触强度的变化,被认为是学习和记忆的基础。突触可塑性长期以来一直是神经元的标志。最近胶质细胞生理学的进展表明,星形胶质细胞和小胶质细胞具有参与和调节各种形式突触可塑性的所有特征。事实上,除了各自的支持和免疫功能外,越来越多的研究表明,星形胶质细胞和小胶质细胞表达大多数神经递质的受体,并释放神经活性物质,这些物质已被证明可以调节神经元活动和突触可塑性。由于神经胶质细胞环绕在突触周围,并且在生理和病理条件下释放多种神经活性分子,因此已经报道神经胶质细胞可以通过多种方式调节突触可塑性。从突触覆盖的变化,到趋化因子和细胞因子的释放,再到专门的“胶质”递质的释放,神经胶质细胞被报道影响突触缩放、同型可塑性、易化可塑性、长时程增强和长时程抑制。

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