首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >A Transgenic Mouse Model to Selectively Identify alpha(3) Na,K-ATPase Expressing Cells in the Nervous System
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A Transgenic Mouse Model to Selectively Identify alpha(3) Na,K-ATPase Expressing Cells in the Nervous System

机译:转基因小鼠模型,以选择性地鉴定神经系统中表达α(3)Na,K-ATP酶的k-ATP酶

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摘要

The alpha(3) Na+,K+-ATPase (alpha(3)NKA) is one of four known alpha isoforms of the mammalian transporter. A deficiency in alpha(3)NKA is linked to severe movement control disorders. Understanding the pathogenesis of these disorders is limited by an incomplete knowledge of alpha(3)NKA expression in the brain as well as the challenges associated with identifying living cells that express the isoform for subsequent electrophysiological studies. To address this problem, transgenic mice were generated on the C57BL/6 genetic background, which utilize the mouse alpha(3) subunit gene (Atp1a3) promoter to drive the expression of ZsGreen1 fluorescent protein. Consistent with published results on alpha(3)NKA distribution, a ZsGreen1 signal was detected in the brain, but not in the liver, with Atp1a3-ZsGreen1 transgenic mice. The intensity of ZsGreen1 fluorescence in neuronal cell bodies varied considerably in the brain, being highest in the brainstem, deep cerebellar and select thalamic nuclei, and relatively weak in cortical regions. Fluorescence was not detected in astrocytes or white matter areas. ZsGreen1-positive neurons were readily observed in fresh (unfixed) brain sections, which were amenable to patch-clamp recordings. Thus, the alpha(3)NKA-ZsGreen1 mouse model provides a powerful tool for studying the distribution and functional properties of alpha(3)NKA-expressing neurons in the brain. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:α(3)Na +,K + -AtPase(α(3)NKA)是哺乳动物转运蛋白的四种已知α同种型中的一种。 α(3)NKA的缺乏与严重运动控制障碍有关。了解这些疾病的发病机制是受到大脑中α(3)NKA表达的不完全知识的限制,以及与鉴定表达同种型的活细胞相关的挑战,用于随后的电生理学研究。为了解决这个问题,在C57BL / 6遗传背景下产生转基因小鼠,其利用小鼠α(3)亚基基因(ATP1A3)启动子来驱动Zsgreen1荧光蛋白的表达。与α(3)NKA分布的公开结果一致,在大脑中检测到Zsgreen1信号,但不在肝脏中,具有ATP1A3-Zsgreen1转基因小鼠。神经元细胞体中Zsgreen1荧光的强度在脑中变化显着,脑干中的最高,深层小脑和选择丘脑核,皮质区域中的相对较弱。在星形胶质细胞或白质区域中未检测到荧光。在新鲜(未固定的)脑切片中容易观察到Zsgreen1阳性神经元,其可用于贴片夹具。因此,α(3)NKA-ZSGreen1小鼠模型提供了一种强大的工具,用于研究脑中α(3)表达NKA的神经元的分布和功能性质。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

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