Suppr超能文献

线粒体、钙通道和肌动蛋白细胞骨架之间的串扰调节蓝斑神经元的去甲肾上腺素能活性。

Crosstalk between mitochondria, calcium channels and actin cytoskeleton modulates noradrenergic activity of locus coeruleus neurons.

机构信息

School of Biomedical Sciences and Pharmacy, University of Newcastle and Hunter Medical Research Institute, Callaghan, NSW, Australia.

Health and Medical Research Group, School of Medicine, University of the Taquari Valley - Univates, Lajeado, RS, Brazil.

出版信息

J Neurochem. 2019 May;149(4):471-487. doi: 10.1111/jnc.14692. Epub 2019 Apr 2.

Abstract

Locus coeruleus (LC) is the name of a group of large sized neurons located at the brain stem, which provides the main source of noradrenaline to the central nervous system, virtually, innervating the whole brain. All noradrenergic signalling provided by this nucleus is dependent on an intrinsic pacemaker process. Our study aims to understand how noradrenergic neurons finely tune their pacemaker processes and regulate their activities. Here we present that mitochondrial perturbation in the LC from mice, inhibits spontaneous firing by a hyperpolarizing response that involves Ca entry via L-type Ca channels and the actin cytoskeleton. We found that pharmacological perturbation of mitochondria from LC neurons using the protonophore carbonyl cyanide m-chlorophenylhydrazone (CCCP), induced a dominant hyperpolarizing response when electrophysiological approaches were performed. Surprisingly, the CCCP-induced hyperpolarizing response was dependent on L-type Ca channel-mediated Ca entry, as it was inhibited by: the removal of extracellular Ca ; the addition of Cd ; nifedipine or nicardipine; but not by the intracellular dialysis with the Ca chelator 1,2-Bis(2-Aminophenoxy)ethane-N,N,N',N'-tetraacetic acid, the latter indicating that the response was not because of a global change in [Ca ] but does not exclude action at intracellular microdomains. Further to this, the incubation of slices with cytochalasin D, an agent that depolymerises the actin cytoskeleton, inhibited the hyperpolarizing response indicating an involvement of the actin cytoskeleton. The data are consistent with the hypothesis that there is a crosstalk between mitochondria and L-type Ca channels leading to modulation of noradrenergic neuronal activity mediated by the actin cytoskeleton. OPEN SCIENCE BADGES: This article has received a badge for Open Materials because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.

摘要

蓝斑(LC)是一组位于脑干的大型神经元的名称,它为中枢神经系统提供去甲肾上腺素的主要来源,实际上,它向整个大脑提供神经支配。这个核团提供的所有去甲肾上腺素能信号都依赖于内在的起搏器过程。我们的研究旨在了解去甲肾上腺素能神经元如何精细地调节其起搏器过程并调节其活动。在这里,我们提出,来自 LC 小鼠的线粒体扰动通过涉及 L 型钙通道和肌动蛋白细胞骨架的钙内流的超极化反应抑制自发放电。我们发现,使用质子载体羰基氰化物 m-氯苯腙(CCCP)对 LC 神经元的线粒体进行药理学扰动时,当进行电生理方法时,会引起主导性超极化反应。令人惊讶的是,CCCP 诱导的超极化反应依赖于 L 型钙通道介导的钙内流,因为它被以下物质抑制:去除细胞外 Ca;添加 Cd;硝苯地平或尼卡地平;但不能通过用 Ca 螯合剂 1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸进行细胞内透析,后者表明该反应不是由于 [Ca]的全局变化,但不排除在细胞内微区的作用。此外,用细胞松弛素 D 孵育切片,一种使肌动蛋白细胞骨架解聚的试剂,抑制了超极化反应,表明肌动蛋白细胞骨架的参与。这些数据与线粒体和 L 型钙通道之间存在串扰的假设一致,导致肌动蛋白细胞骨架介导的去甲肾上腺素能神经元活性的调节。开放科学徽章:本文因提供了重现手稿中研究所需的所有相关信息而获得了“开放材料”徽章。本文的完整开放科学披露表格可在文章末尾找到。有关开放实践徽章的更多信息,请访问 https://cos.io/our-services/open-science-badges/。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验