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细胞外ATP对泛连接蛋白1表面表达的调节:对健康和疾病状态下神经系统功能的潜在影响

Regulation of Pannexin 1 Surface Expression by Extracellular ATP: Potential Implications for Nervous System Function in Health and Disease.

作者信息

Swayne Leigh A, Boyce Andrew K J

机构信息

Division of Medical Sciences and Island Medical Program, University of Victoria, VictoriaBC, Canada.

Department of Cellular and Physiological Sciences, University of British Columbia, VancouverBC, Canada.

出版信息

Front Cell Neurosci. 2017 Aug 8;11:230. doi: 10.3389/fncel.2017.00230. eCollection 2017.

Abstract

Pannexin 1 (Panx1) channels are widely recognized for their role in ATP release, and as follows, their function is closely tied to that of ATP-activated P2X7 purinergic receptors (P2X7Rs). Our recent work has shown that extracellular ATP induces clustering of Panx1 with P2X7Rs and their subsequent internalization through a non-canonical cholesterol-dependent mechanism. In other words, we have demonstrated that extracellular ATP levels can regulate the cell surface expression of Panx1. Here we discuss two situations in which we hypothesize that ATP modulation of Panx1 surface expression could be relevant for central nervous system function. The first scenario involves the development of new neurons in the ventricular zone. We propose that ATP-induced Panx1 endocytosis could play an important role in regulating the balance of cell proliferation, survival, and differentiation within this neurogenic niche in the healthy brain. The second scenario relates to the spinal cord, in which we posit that an impairment of ATP-induced Panx1 endocytosis could contribute to pathological neuroplasticity. Together, the discussion of these hypotheses serves to highlight important outstanding questions regarding the interplay between extracellular ATP, Panx1, and P2X7Rs in the nervous system in health and disease.

摘要

泛连接蛋白1(Panx1)通道因其在ATP释放中的作用而被广泛认可,因此,其功能与ATP激活的嘌呤能P2X7受体(P2X7Rs)密切相关。我们最近的研究表明,细胞外ATP可诱导Panx1与P2X7Rs聚集,并通过非经典的胆固醇依赖性机制使其内化。换句话说,我们已经证明细胞外ATP水平可以调节Panx1的细胞表面表达。在此,我们讨论两种情况,我们假设ATP对Panx1表面表达的调节可能与中枢神经系统功能相关。第一种情况涉及脑室区新神经元的发育。我们提出,ATP诱导的Panx1内吞作用可能在调节健康大脑中这个神经发生微环境内细胞增殖、存活和分化的平衡方面发挥重要作用。第二种情况与脊髓有关,我们假设ATP诱导的Panx1内吞作用受损可能导致病理性神经可塑性。总之,对这些假设的讨论有助于突出关于细胞外ATP、Panx1和P2X7Rs在健康和疾病状态下神经系统中相互作用方面的重要悬而未决的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b6/5550711/4d9c9c61942e/fncel-11-00230-g001.jpg

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