Llorens-Martín María, Jurado Jerónimo, Hernández Félix, Avila Jesús
Centro de Biología Molecular "Severo Ochoa", Consejo Superior de Investigaciones Cientificas, Universidad Autónoma de Madrid Madrid, Spain ; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Instituto de Salud Carlos III Madrid, Spain.
Centro de Biología Molecular "Severo Ochoa", Consejo Superior de Investigaciones Cientificas, Universidad Autónoma de Madrid Madrid, Spain ; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Instituto de Salud Carlos III Madrid, Spain ; Biology Faculty, Autónoma University Madrid, Spain.
Front Mol Neurosci. 2014 May 21;7:46. doi: 10.3389/fnmol.2014.00046. eCollection 2014.
Alzheimer disease (AD) is the most common form of age-related dementia. The etiology of AD is considered to be multifactorial as only a negligible percentage of cases have a familial or genetic origin. Glycogen synthase kinase-3 (GSK-3) is regarded as a critical molecular link between the two histopathological hallmarks of the disease, namely senile plaques and neurofibrillary tangles. In this review, we summarize current data regarding the involvement of this kinase in several aspects of AD development and progression, as well as key observations highlighting GSK-3 as one of the most relevant targets for AD treatment.
阿尔茨海默病(AD)是与年龄相关的痴呆最常见的形式。AD的病因被认为是多因素的,因为只有可忽略不计的病例比例具有家族性或遗传性起源。糖原合酶激酶-3(GSK-3)被视为该疾病两个组织病理学特征(即老年斑和神经原纤维缠结)之间的关键分子联系。在本综述中,我们总结了有关该激酶参与AD发生和进展的几个方面的当前数据,以及突出显示GSK-3作为AD治疗最相关靶点之一的关键观察结果。