The Role of Mitochondrial Pyruvate Carrier in Neurological Disorders.

IF 4.6 2区 医学 Q1 NEUROSCIENCES Molecular Neurobiology Pub Date : 2025-03-01 Epub Date: 2024-08-23 DOI:10.1007/s12035-024-04435-7
Yue Liu, Xiying Yu, Wei Jiang
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Abstract

The mitochondrial pyruvate carrier (MPC) is a specific protein complex located in the inner mitochondrial membrane. Comprising a heterodimer of two homodimeric membrane proteins, mitochondrial pyruvate carrier 1 and mitochondrial pyruvate carrier 2, MPC connects cytoplasmic metabolism to mitochondrial metabolism by transferring pyruvate from the cytoplasm to the mitochondria. The nervous system requires substantial energy to maintain its function, and the mitochondrial energy supply is closely linked to neurological function. Mitochondrial dysfunction can induce or exacerbate intracerebral pathologies. MPC influences mitochondrial function due to its specific role as a pyruvate transporter. However, recent studies on MPC and mitochondrial dysfunction in neurological disorders have yielded controversial results, and the underlying mechanisms remain unclear. In this brief review, we provide an overview of the structure and function of MPC. We further discuss the potential mechanisms and feasibility of targeting MPC in treating Parkinson's disease, Alzheimer's disease, and cerebral ischemia/hypoxia injury. This review aims to offer insights into MPC as a target for clinical treatment.

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线粒体丙酮酸载体在神经系统疾病中的作用。
线粒体丙酮酸载体(MPC)是位于线粒体内膜的一种特殊蛋白质复合体。MPC 由线粒体丙酮酸载体 1 和线粒体丙酮酸载体 2 这两个同源膜蛋白的异源二聚体组成,通过将丙酮酸从细胞质转移到线粒体,将细胞质代谢与线粒体代谢连接起来。神经系统需要大量能量来维持其功能,而线粒体的能量供应与神经功能密切相关。线粒体功能障碍可诱发或加重脑内病变。MPC 由于其作为丙酮酸转运体的特殊作用而对线粒体功能产生影响。然而,近期有关神经系统疾病中 MPC 和线粒体功能障碍的研究结果存在争议,其潜在机制仍不清楚。在这篇简短的综述中,我们概述了 MPC 的结构和功能。我们将进一步讨论针对 MPC 治疗帕金森病、阿尔茨海默病和脑缺血/缺氧损伤的潜在机制和可行性。本综述旨在深入探讨将 MPC 作为临床治疗靶点的问题。
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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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