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皮质抑制性突触的生物化学解剖。

The biochemical anatomy of cortical inhibitory synapses.

机构信息

Howard Hughes Medical Institute, Laboratory of Molecular Biology, The Rockefeller University, New York, New York, United States of America.

出版信息

PLoS One. 2012;7(6):e39572. doi: 10.1371/journal.pone.0039572. Epub 2012 Jun 29.

Abstract

Classical electron microscopic studies of the mammalian brain revealed two major classes of synapses, distinguished by the presence of a large postsynaptic density (PSD) exclusively at type 1, excitatory synapses. Biochemical studies of the PSD have established the paradigm of the synapse as a complex signal-processing machine that controls synaptic plasticity. We report here the results of a proteomic analysis of type 2, inhibitory synaptic complexes isolated by affinity purification from the cerebral cortex. We show that these synaptic complexes contain a variety of neurotransmitter receptors, neural cell-scaffolding and adhesion molecules, but that they are entirely lacking in cell signaling proteins. This fundamental distinction between the functions of type 1 and type 2 synapses in the nervous system has far reaching implications for models of synaptic plasticity, rapid adaptations in neural circuits, and homeostatic mechanisms controlling the balance of excitation and inhibition in the mature brain.

摘要

经典的电子显微镜研究哺乳动物大脑揭示了两类主要的突触,其区别在于 1 型兴奋性突触存在一个大的突触后密度(PSD)。PSD 的生化研究确立了突触作为一个复杂的信号处理机器的范例,控制着突触可塑性。我们在这里报告了通过亲和纯化从大脑皮层中分离的 2 型抑制性突触复合物的蛋白质组学分析结果。我们表明,这些突触复合物含有各种神经递质受体、神经细胞支架和粘附分子,但完全缺乏细胞信号蛋白。这种在神经系统中 1 型和 2 型突触功能之间的根本区别,对突触可塑性模型、神经网络的快速适应以及控制成熟大脑中兴奋和抑制平衡的动态平衡机制具有深远的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b2/3387162/d706b3de8bf8/pone.0039572.g001.jpg

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