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关于大阳离子通过ATP门控P2X受体渗透的新见解。

New Insights Into Permeation of Large Cations Through ATP-Gated P2X Receptors.

作者信息

Peverini Laurie, Beudez Juline, Dunning Kate, Chataigneau Thierry, Grutter Thomas

机构信息

CNRS, CAMB UMR 7199, Équipe de Chimie et Neurobiologie Moléculaire, Université de Strasbourg, Strasbourg, France.

出版信息

Front Mol Neurosci. 2018 Jul 31;11:265. doi: 10.3389/fnmol.2018.00265. eCollection 2018.

Abstract

The permeability of large cations through the P2X pore has remained arguably the most controversial and complicated topic in P2X-related research, with the emergence of conflicting studies on the existence, mechanism and physiological relevance of a so-called "dilated" state. Due to the important role of several "dilating" P2X subtypes in numerous diseases, a clear and detailed understanding of this phenomenon represents a research priority. Recent advances, however, have challenged the existence of a progressive, ATP-induced pore dilation, by demonstrating that this phenomenon is an artifact of the method employed. Here, we discuss briefly the history of this controversial and enigmatic dilated state, from its initial discovery to its recent reconsideration. We will discuss the literature in which mechanistic pathways to a large cation-permeable state are proposed, as well as important advances in the methodology employed to study this elusive state. Considering recent literature, we will also open the discussion as to whether an intrinsically dilating P2X pore exists, as well as the physiological relevance of such a large cation-permeable pore and its potential use as therapeutic pathway.

摘要

大阳离子通过P2X孔道的通透性一直是P2X相关研究中最具争议和最复杂的话题,关于所谓“扩张”状态的存在、机制和生理相关性出现了相互矛盾的研究。由于几种“扩张型”P2X亚型在众多疾病中发挥重要作用,清晰而详细地了解这一现象是研究的重点。然而,最近的进展对ATP诱导的渐进性孔道扩张的存在提出了挑战,表明这一现象是所用方法的人为产物。在此,我们简要讨论这一有争议且神秘的扩张状态的历史,从其最初发现到最近的重新审视。我们将讨论提出通向大阳离子通透状态的机制途径的文献,以及用于研究这一难以捉摸状态的方法学的重要进展。考虑到最近的文献,我们还将展开讨论是否存在内在扩张的P2X孔道,以及这种大阳离子通透孔道的生理相关性及其作为治疗途径的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ace/6080412/cd2d8fa1e694/fnmol-11-00265-g0001.jpg

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