Pchitskaya E I, Zhemkov V A, Bezprozvanny I B
Laboratory of Molecular Neurodegeneration, Department of Medical Physics, Peter the Great St. Petersburg Polytechnic University, St. Petersburg, 195251, Russia.
Department of Physiology, UT Southwestern Medical Center at Dallas, 75390 Dallas, TX, USA.
Biochemistry (Mosc). 2018 Sep;83(9):1068-1074. doi: 10.1134/S0006297918090080.
Alzheimer's disease (AD) is the most common incurable neurodegenerative disorder that affects the processes of memory formation and storage. The loss of dendritic spines and alteration in their morphology in AD correlate with the extent of patient's cognitive decline. Tubulin had been believed to be restricted to dendritic shafts, until recent studies demonstrated that dynamically growing tubulin microtubules enter dendritic spines and promote their maturation. Abnormalities of tubulin cytoskeleton may contribute to the process of dendritic spine shape alteration and their subsequent loss in AD. In this review, association between tubulin cytoskeleton dynamics and dendritic spine morphology is discussed in the context of dendritic spine alterations in AD. Potential implications of these findings for the development of AD therapy are proposed.
阿尔茨海默病(AD)是最常见的不可治愈的神经退行性疾病,它会影响记忆形成和存储过程。AD患者树突棘的丧失及其形态改变与患者认知能力下降的程度相关。一直以来,人们认为微管蛋白仅存在于树突轴中,直到最近的研究表明,动态生长的微管蛋白微管会进入树突棘并促进其成熟。微管蛋白细胞骨架的异常可能会导致AD中树突棘形状改变及其随后的丧失。在这篇综述中,我们将在AD树突棘改变的背景下讨论微管蛋白细胞骨架动力学与树突棘形态之间的关联。本文还提出了这些发现对AD治疗发展的潜在意义。