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蛋白质稳态与运动单位疾病

Proteostasis and Diseases of the Motor Unit.

作者信息

Rinaldi Carlo, Mäger Imre, Wood Matthew J

机构信息

Department of Physiology, Anatomy and Genetics, University of Oxford Oxford, UK.

出版信息

Front Mol Neurosci. 2016 Dec 27;9:164. doi: 10.3389/fnmol.2016.00164. eCollection 2016.

Abstract

The accumulation in neurons of aberrant protein species, the pathological hallmark of many neurodegenerative diseases, results from a global impairment of key cellular processes governing protein synthesis/degradation and repair mechanisms, also known as the proteostasis network (PN). The growing number of connections between dysfunction of this intricate network of pathways and diseases of the motor unit, where both motor neurons and muscle are primarily affected, has provided momentum to investigate the muscle- and motor neuron-specific response to physiological and pathological stressors and to explore the therapeutic opportunities that manipulation of this process may offer. Furthermore, these diseases offer an unparalleled opportunity to deepen our understanding of the molecular mechanisms behind the intertissue communication and transfer of signals of proteostasis. The most compelling aspect of these investigations is their immediate potential for therapeutic impact: targeting muscle to stem degeneration of the motor unit would represent a dramatic paradigm therapeutic shift for treating these devastating diseases. Here we will review the current state of the art of the research on the alterations of the PN in diseases of the motor unit and its potential to result in effective treatments for these devastating neuromuscular disorders.

摘要

异常蛋白质种类在神经元中的积累是许多神经退行性疾病的病理标志,这是由于控制蛋白质合成/降解和修复机制的关键细胞过程出现整体损伤所致,这些过程也被称为蛋白质稳态网络(PN)。这个错综复杂的通路网络功能障碍与运动单位疾病之间的联系日益增多,运动单位中运动神经元和肌肉均受到主要影响,这为研究肌肉和运动神经元对生理和病理应激源的特异性反应以及探索操纵这一过程可能带来的治疗机会提供了动力。此外,这些疾病为深入理解蛋白质稳态信号在组织间通讯和传递背后的分子机制提供了无与伦比的机会。这些研究最引人注目的方面在于其对治疗的直接潜在影响:针对肌肉来阻止运动单位的退化将代表治疗这些毁灭性疾病的一种巨大的治疗范式转变。在此,我们将综述运动单位疾病中PN改变的研究现状及其产生针对这些毁灭性神经肌肉疾病的有效治疗方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da6b/5187379/7dcc48c2ec7e/fnmol-09-00164-g001.jpg

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