蛋白质稳态
肌萎缩侧索硬化
蛋白质组
神经科学
机制(生物学)
生物
疾病
损失函数
生物信息学
医学
遗传学
基因
表型
病理
哲学
认识论
作者
Isabella A. Lambert-Smith,Darren N. Saunders,Justin J. Yerbury
标识
DOI:10.1016/j.pbiomolbio.2022.06.001
摘要
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and fatal neurodegenerative disease that results from the loss of both upper and lower motor neurons. It is the most common motor neuron disease and currently has no effective treatment. There is mounting evidence to suggest that disturbances in proteostasis play a significant role in ALS pathogenesis. Proteostasis is the maintenance of the proteome at the right level, conformation and location to allow a cell to perform its intended function. In this review, we present a thorough synthesis of the literature that provides evidence that genetic mutations associated with ALS cause imbalance to a proteome that is vulnerable to such pressure due to its metastable nature. We propose that the mechanism underlying motor neuron death caused by defects in mRNA metabolism and protein degradation pathways converges on proteostasis dysfunction. We propose that the proteostasis network may provide an effective target for therapeutic development in ALS.
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