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双色受激发射损耗显微镜揭示了成年和老年小鼠活动区中巴松管蛋白和短笛蛋白的夹心结构。

Dual-color STED microscopy reveals a sandwich structure of Bassoon and Piccolo in active zones of adult and aged mice.

作者信息

Nishimune Hiroshi, Badawi Yomna, Mori Shuuichi, Shigemoto Kazuhiro

机构信息

Department of Anatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, 66160, USA.

Department of Geriatric Medicine, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku, Tokyo 173-0015, Japan.

出版信息

Sci Rep. 2016 Jun 20;6:27935. doi: 10.1038/srep27935.

Abstract

Presynaptic active zones play a pivotal role as synaptic vesicle release sites for synaptic transmission, but the molecular architecture of active zones in mammalian neuromuscular junctions (NMJs) at sub-diffraction limited resolution remains unknown. Bassoon and Piccolo are active zone specific cytosolic proteins essential for active zone assembly in NMJs, ribbon synapses, and brain synapses. These proteins are thought to colocalize and share some functions at active zones. Here, we report an unexpected finding of non-overlapping localization of these two proteins in mouse NMJs revealed using dual-color stimulated emission depletion (STED) super resolution microscopy. Piccolo puncta sandwiched Bassoon puncta and aligned in a Piccolo-Bassoon-Piccolo structure in adult NMJs. P/Q-type voltage-gated calcium channel (VGCC) puncta colocalized with Bassoon puncta. The P/Q-type VGCC and Bassoon protein levels decreased significantly in NMJs from aged mouse. In contrast, the Piccolo levels in NMJs from aged mice were comparable to levels in adult mice. This study revealed the molecular architecture of active zones in mouse NMJs at sub-diffraction limited resolution, and described the selective degeneration mechanism of active zone proteins in NMJs from aged mice. Interestingly, the localization pattern of active zone proteins described herein is similar to active zone structures described using electron microscope tomography.

摘要

突触前活跃区作为突触传递中突触小泡释放的位点发挥着关键作用,但在亚衍射极限分辨率下,哺乳动物神经肌肉接头(NMJ)中活跃区的分子结构仍不清楚。巴松管蛋白(Bassoon)和短笛蛋白(Piccolo)是活跃区特异性胞质蛋白,对NMJ、带状突触和脑突触中的活跃区组装至关重要。这些蛋白被认为在活跃区共定位并共享一些功能。在此,我们报告了一项意外发现,利用双色受激发射损耗(STED)超分辨率显微镜揭示了这两种蛋白在小鼠NMJ中的非重叠定位。在成年NMJ中,短笛蛋白斑点夹在巴松管蛋白斑点之间,并以短笛-巴松管-短笛结构排列。P/Q型电压门控钙通道(VGCC)斑点与巴松管蛋白斑点共定位。老年小鼠NMJ中P/Q型VGCC和巴松管蛋白水平显著降低。相比之下,老年小鼠NMJ中的短笛蛋白水平与成年小鼠相当。这项研究揭示了亚衍射极限分辨率下小鼠NMJ中活跃区的分子结构,并描述了老年小鼠NMJ中活跃区蛋白的选择性退化机制。有趣的是,本文所述的活跃区蛋白定位模式与使用电子显微镜断层扫描描述的活跃区结构相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e900/4913281/db956f3de5ce/srep27935-f1.jpg

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