Faculty of Science, University of Stellenbosch, Stellenbosch, South Africa.
Faculty of Science, University of Stellenbosch, Stellenbosch, South Africa.
Int Rev Cell Mol Biol. 2018;336:321-361. doi: 10.1016/bs.ircmb.2017.07.002. Epub 2017 Sep 6.
The fine control of neuronal proteostasis is an essential element that preserves cell viability. Advancing age is a major risk factor for Alzheimer's disease (AD), and autophagy is thought to dictate normal and pathological aging through intricate molecular machinery controlling protein aggregation. Although the role of autophagy dysfunction in AD is known, the dynamic changes during the progression of the disease remain unclear. Recent studies have provided new insight into the molecular mechanisms that link defective autophagy and cellular fate, underscoring the pathogenic events associated with AD. Here, we will focus on recent studies that underpin a distinct role for autophagy deficits and highly localized autophagic defects, impacting primarily the amyloidogenic pathway activity. By uniquely assessing the dynamic changes in key proteins during the disease progression in the context of the autophagy machinery function and amyloid beta toxicity, specifically, a connect between protein degradation failure and cell death susceptibility is revealed which may suggest new avenues for the development of better targeted therapeutic interventions.
神经元蛋白稳态的精细控制是维持细胞活力的重要因素。年龄增长是阿尔茨海默病(AD)的主要危险因素,自噬通过控制蛋白质聚集的复杂分子机制来决定正常和病理性衰老。虽然自噬功能障碍在 AD 中的作用已被人们所了解,但疾病进展过程中的动态变化仍不清楚。最近的研究为连接自噬缺陷和细胞命运的分子机制提供了新的见解,强调了与 AD 相关的发病事件。在这里,我们将重点关注最近的研究,这些研究为自噬缺陷和高度局部化的自噬缺陷的独特作用提供了依据,主要影响淀粉样蛋白途径的活性。通过在自噬机制功能和β淀粉样蛋白毒性的背景下,专门评估疾病进展过程中关键蛋白的动态变化,揭示了蛋白降解失败和细胞死亡易感性之间的联系,这可能为开发更好的靶向治疗干预提供新途径。