哺乳动物中枢神经系统轴突初始段连接蛋白36的定位。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2020-12-15 eCollection Date: 2020-01-01
Deepthi Thomas, Joanne Mm Senecal, Bruce D Lynn, Roger D Traub, James I Nagy
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摘要

在哺乳动物中枢神经系统(CNS)中,由间隙连接形成的电突触存在于多种神经元亚细胞位点,包括体细胞、树突和轴突末端室。大量使用小鼠和大鼠进行的电生理学研究,以及计算机建模方法,已经预测了轴突之间在它们从神经元躯体出现附近的额外电突触的发生。在这里,我们使用免疫荧光方法寻找神经元间隙连接形成蛋白connexin36 (Cx36)沿轴突初始段(AIS标记ankyrinG)的定位。在小鼠的几个中枢神经系统区域,包括脊髓、下橄榄和大脑皮层,发现免疫荧光Cx36-puncta与ais有关。通过共聚焦单扫描和三维成像、免疫荧光强度谱和高分辨率结构照明显微镜(SIM)证实了cx36 -点在ais处的定位。长度达30µm的ais通常显示单个cx36 -点状点,这些显示cx36 -点状点的长ais在下橄榄和大脑皮层各层的发生率从3%到7%不等。在下橄榄中,间隙连接相关蛋白zonula occludens-1 (ZO-1)被发现与AISs上的Cx36-puncta共定位,表明这些点具有间隙连接的一些分子成分。我们的研究结果增加了Cx36被部署的神经元亚细胞位置,并提出了它参与AIS区新功能的可能性。
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Connexin36 localization along axon initial segments in the mammalian CNS.

Electrical synapses formed by gap junctions occur at a variety of neuronal subcellular sites in the mammalian central nervous system (CNS), including at somatic, dendritic and axon terminal compartments. Numerous electrophysiological studies using mice and rats, as well as computer modelling approaches, have predicted the additional occurrence of electrical synapses between axons near their emergence from neuronal somata. Here, we used immunofluorescence methods to search for localization of the neuronal gap junction-forming protein connexin36 (Cx36) along axon initial segments (AISs) labelled for the AIS marker ankyrinG. Immunofluorescent Cx36-puncta were found to be associated with AISs in several CNS regions of mice, including the spinal cord, inferior olive and cerebral cortex. Localization of Cx36-puncta at AISs was confirmed by confocal single scan and 3D imaging, immunofluorescence intensity profiling and high resolution structured illumination microscopy (SIM). AISs measuring up to 30 µm in length displayed typically a single Cx36-punctum and the incidence of these long AISs displaying Cx36-puncta ranged from 3% to 7% in the inferior olive and in various layers of the cerebral cortex. In the inferior olive, the gap junction associated protein zonula occludens-1 (ZO-1) was found to be co-localized with Cx36-puncta on AISs, indicating that these puncta have some of the molecular constituents of gap junctions. Our results add to the neuronal subcellular locations at which Cx36 is deployed, and raise possibilities for its involvement in novel functions in the AIS compartment.

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