首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Cell-type-specific roles of Na~+/K~+ ATPase subunits in Drosophila auditory mechanosensation
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Cell-type-specific roles of Na~+/K~+ ATPase subunits in Drosophila auditory mechanosensation

机译:Na〜+ / K〜+ ATPase亚基在果蝇听觉机械感觉中的细胞类型特异性作用

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摘要

Ion homeostasis is a fundamental cellular process particularly important in excitable cell activities such as hearing. It relies on the Na~+/K~+ ATPase (also referred to as the Na pump), which is composed of a catalytic a subunit and a p subunit required for its transport to the plasma membrane and for regulating its activity. We show that α and β subunits are expressed in Johnston's organ (JO), the Drosophila auditory organ. We knocked down expression of a subunits (ATPα and α-like) and β subunits (nrv1, nrv2, and nrv3) individually in JO with UAS/Gal4-mediated RNAi. ATPa shows elevated expression in the ablumenal membrane of scolopale cells, which enwrap JO neuronal dendrites in endolymph-like compartments. Knocking down ATPa, but not α-like. in the entire JO or only in scolopale cells using specific drivers, resulted in complete deafness. Among β subunits, nrv2 is expressed in scolopale cells and nrv3 in JO neurons. Knocking down nrv2 in scolopale cells blocked Nrv2 expression, reduced ATPα expression in the scolopale cells, and caused almost complete deafness. Furthermore, knockdown of either nrv2 or ATPa specifically in scolopale cells causes abnormal, electron-dense material accumulation in the scolopale space. Similarly, nrv3 functions in JO but not in scolopale cells, suggesting neuron specificity that parallels nrv2 scolopale cell-specific support of the catalytic ATPa. Our studies provide an amenable model to investigate generation of endolymph-like extracellular compartments.
机译:离子稳态是基本的细胞过程,在兴奋性细胞活动(例如听力)中尤其重要。它依赖于Na〜+ / K〜+ ATPase(也称为Na泵),它由一个催化亚基和一个p亚基组成,该亚基被运输到质膜并调节其活性。我们显示α和β亚基在果蝇听觉器官约翰斯顿的器官(JO)中表达。我们通过UAS / Gal4介导的RNAi敲低了JO中一个亚基(ATPα和α-样)和β亚基(nrv1,nrv2和nrv3)的表达。 ATPa在骨细胞的空泡膜中显示出升高的表达,这将JO神经元树突包裹在内淋巴样隔室中。击倒ATPa,但不像α。使用特定的驱动程序在整个JO中或仅在骨细胞中导致完全耳聋。在β亚基中,nrv2在骨细胞中表达,nrv3在JO神经元中表达。在骨细胞中敲低nrv2会阻断Nrv2表达,降低the骨细胞中ATPα的表达,并导致几乎完全耳聋。此外,nrv2或ATPa的敲低,特别是在细胞中,会导致在abnormal空间中异常的电子致密物质积聚。同样,nrv3在JO中起作用,但在骨细胞中则不起作用,这表明神经元特异性与催化性ATPa的nrv2 sco骨细胞特异性支持相似。我们的研究提供了一个合适的模型来研究内淋巴样细胞外区室的产生。

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