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小鼠和人类皮质突触的超微结构膜动力学

Ultrastructural membrane dynamics of mouse and human cortical synapses.

作者信息

Eddings Chelsy R, Fan Minghua, Imoto Yuuta, Itoh Kie, McDonald Xiomara, Eilers Jens, Anderson William S, Worley Paul F, Lippmann Kristina, Nauen David W, Watanabe Shigeki

机构信息

Department of Cell Biology, The Johns Hopkins University, Baltimore MD, 21205, USA.

Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University, Baltimore MD, 21205, USA.

出版信息

bioRxiv. 2024 Dec 26:2024.12.26.630393. doi: 10.1101/2024.12.26.630393.

Abstract

Live human brain tissues provide unique opportunities for understanding the physiology and pathophysiology of synaptic transmission. Investigations have been limited to anatomy, electrophysiology, and protein localization-while crucial parameters such as synaptic vesicle dynamics were not visualized. Here we utilize zap-and-freeze time-resolved electron microscopy to overcome this hurdle. First we validate the approach with acute mouse brain slices to demonstrate that axons parallel to the electrical field can be stimulated to produce calcium signaling. Next we show that ultrafast endocytosis is induced and can be captured in both mouse and human brain slices. Crucially, in both species a protein essential for ultrafast endocytosis Dynamin 1xA (Dyn1xA) localizes to the region peripheral to the active zone, the putative endocytic zone, indicating a likely mechanism conservation between mouse and human. This approach has the potential to reveal dynamic, high-resolution information about synaptic membrane trafficking in intact human brain slices.

摘要

活的人脑组织为理解突触传递的生理学和病理生理学提供了独特的机会。此前的研究仅限于解剖学、电生理学和蛋白质定位,而诸如突触小泡动力学等关键参数并未可视化。在此,我们利用“电击-冷冻”时间分辨电子显微镜来克服这一障碍。首先,我们用急性小鼠脑切片验证该方法,以证明与电场平行的轴突可以被刺激产生钙信号。接下来,我们表明超快内吞作用会被诱导,并且可以在小鼠和人脑切片中被捕获。至关重要的是,在这两个物种中,超快内吞作用所必需的一种蛋白质——发动蛋白1xA(Dyn1xA)定位于活性区周围的区域,即假定的内吞区,这表明小鼠和人之间可能存在机制保守性。这种方法有潜力揭示完整人脑切片中突触膜运输的动态、高分辨率信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf92/11703259/f4329055209b/nihpp-2024.12.26.630393v1-f0001.jpg

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