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溶酶体中的酸门。

The Acid Gate in the Lysosome.

机构信息

Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, China.

Department of Molecular, Cellular, and Developmental Biology, University of Michigan, 4114 Biological Sciences Building (BSB), 1105 N. University Ave, Ann Arbor, MI, USA.

出版信息

Autophagy. 2023 Apr;19(4):1368-1370. doi: 10.1080/15548627.2022.2125629. Epub 2022 Sep 29.

Abstract

The acidic environment within lysosomes is maintained within a narrow pH range (pH 4.5-5.0) optimal for digesting autophagic cargo macromolecules so that the resulting building block metabolites can be reused. This pH homeostasis is a consequence of proton influx produced by a V-type H-translocating ATPase (V-ATPase) and rapid proton efflux through an unidentified "leak" pathway. By performing a candidate expression screening, we discovered that the gene encodes a proton-activated, proton-selective channel (LyPAP) that is required for lysosomal H "leak" currents. The activity of LyPAP is most active when lysosomes are hyper-acidified, and cells lacking TMEM175 exhibit lysosomal hyper-acidification and impaired proteolytic degradation, both of which can be restored by optimizing lysosomal pH using pharmacological agents. Variants of that are associated with susceptibility to Parkinson disease (PD) cause a reduction in TMEM175-dependent LyPAP currents and lysosomal hyper-acidification. Hence, our studies not only reveal an essential H-dissipating pathway in lysosomes, but also provide a molecular target to regulate pH-dependent lysosomal functions and associated pathologies.

摘要

溶酶体内部的酸性环境维持在一个狭窄的 pH 范围内(pH4.5-5.0),这个 pH 值最有利于消化自噬货物大分子,从而使产生的构建块代谢物可以被重复利用。这种 pH 平衡是质子流入的结果,质子由 V 型 H 转运 ATP 酶(V-ATPase)产生,而通过一个未识别的“泄漏”途径快速排出质子。通过进行候选表达筛选,我们发现该基因编码一种质子激活的质子选择性通道(LyPAP),该通道对于溶酶体 H“泄漏”电流是必需的。当溶酶体过度酸化时,LyPAP 的活性最高,而缺乏 TMEM175 的细胞则表现出溶酶体过度酸化和蛋白酶降解受损,这两种情况都可以通过使用药理学药物优化溶酶体 pH 来恢复。与帕金森病(PD)易感性相关的变体导致 TMEM175 依赖性 LyPAP 电流和溶酶体过度酸化减少。因此,我们的研究不仅揭示了溶酶体中一种必需的 H 耗散途径,还为调节 pH 依赖性溶酶体功能和相关病理提供了一个分子靶点。

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本文引用的文献

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