Institute of Pharmacology, Medical Faculty Heidelberg, Heidelberg University, 69120 Heidelberg, Germany.
Cells. 2022 Oct 27;11(21):3395. doi: 10.3390/cells11213395.
Neurodegenerative diseases (NDDs) are irreversible, progressive diseases with no effective treatment. The hallmark of NDDs is the aggregation of misfolded, modified proteins, which impair neuronal vulnerability and cause brain damage. The loss of synaptic connection and the progressive loss of neurons result in cognitive defects. Several dysregulated proteins and overlapping molecular mechanisms contribute to the pathophysiology of NDDs. Post-translational modifications (PTMs) are essential regulators of protein function, trafficking, and maintaining neuronal hemostasis. The conjugation of a small ubiquitin-like modifier (SUMO) is a reversible, dynamic PTM required for synaptic and cognitive function. The onset and progression of neurodegenerative diseases are associated with aberrant SUMOylation. In this review, we have summarized the role of SUMOylation in regulating critical proteins involved in the onset and progression of several NDDs.
神经退行性疾病(NDDs)是不可逆转的、进行性疾病,目前尚无有效治疗方法。NDD 的特征是错误折叠、修饰的蛋白质聚集,损害神经元易损性并导致大脑损伤。突触连接的丧失和神经元的进行性丧失导致认知缺陷。几种失调的蛋白质和重叠的分子机制导致了 NDD 的病理生理学。翻译后修饰(PTMs)是蛋白质功能、运输和维持神经元止血的重要调节剂。小分子泛素样修饰物(SUMO)的连接是一种可逆的、动态的 PTM,对于突触和认知功能是必需的。神经退行性疾病的发作和进展与异常的 SUMO 化有关。在这篇综述中,我们总结了 SUMO 化在调节几种 NDD 发病和进展过程中涉及的关键蛋白质中的作用。