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关联荧光与高分辨率扫描电子显微镜(HRSEM)用于研究抑制性突触可塑性诱导的GABA受体聚集。

Correlating Fluorescence and High-Resolution Scanning Electron Microscopy (HRSEM) for the study of GABA receptor clustering induced by inhibitory synaptic plasticity.

作者信息

Orlando Marta, Ravasenga Tiziana, Petrini Enrica Maria, Falqui Andrea, Marotta Roberto, Barberis Andrea

机构信息

Neuroscience and Brain Technologies Department, Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163, Genoa, Italy.

Institute of Neurophysiology, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany.

出版信息

Sci Rep. 2017 Oct 23;7(1):13768. doi: 10.1038/s41598-017-14210-5.

Abstract

Both excitatory and inhibitory synaptic contacts display activity dependent dynamic changes in their efficacy that are globally termed synaptic plasticity. Although the molecular mechanisms underlying glutamatergic synaptic plasticity have been extensively investigated and described, those responsible for inhibitory synaptic plasticity are only beginning to be unveiled. In this framework, the ultrastructural changes of the inhibitory synapses during plasticity have been poorly investigated. Here we combined confocal fluorescence microscopy (CFM) with high resolution scanning electron microscopy (HRSEM) to characterize the fine structural rearrangements of post-synaptic GABA Receptors (GABARs) at the nanometric scale during the induction of inhibitory long-term potentiation (iLTP). Additional electron tomography (ET) experiments on immunolabelled hippocampal neurons allowed the visualization of synaptic contacts and confirmed the reorganization of post-synaptic GABAR clusters in response to chemical iLTP inducing protocol. Altogether, these approaches revealed that, following the induction of inhibitory synaptic potentiation, GABAR clusters increase in size and number at the post-synaptic membrane with no other major structural changes of the pre- and post-synaptic elements.

摘要

兴奋性和抑制性突触连接在其效能上均表现出依赖于活动的动态变化,这些变化统称为突触可塑性。尽管谷氨酸能突触可塑性的分子机制已得到广泛研究和描述,但负责抑制性突触可塑性的机制才刚刚开始被揭示。在此框架下,可塑性过程中抑制性突触的超微结构变化研究较少。在这里,我们将共聚焦荧光显微镜(CFM)与高分辨率扫描电子显微镜(HRSEM)相结合,以在纳米尺度上表征抑制性长时程增强(iLTP)诱导过程中突触后γ-氨基丁酸受体(GABARs)的精细结构重排。对免疫标记的海马神经元进行的额外电子断层扫描(ET)实验使突触连接可视化,并证实了化学iLTP诱导方案后突触后GABAR簇的重组。总之,这些方法表明,在诱导抑制性突触增强后,突触后膜上的GABAR簇在大小和数量上增加,而突触前和突触后元件没有其他主要结构变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e93/5653763/b3bcf5a0c8dd/41598_2017_14210_Fig1_HTML.jpg

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