Bondareff W, Harrington C R, Wischik C M, Hauser D L, Roth M
Department of Psychiatry and the Behavioral Sciences, University of Southern California Medical School, Los Angeles 90033, USA.
J Neuropathol Exp Neurol. 1995 Sep;54(5):657-63. doi: 10.1097/00005072-199509000-00007.
Adult human nerve cells contain tau protein, a phosphorylated microtubule-associated protein, that is hyperphosphorylated in the fetus and in patients with Alzheimer's disease. Hyperphosphorylation, which diminishes the microtubule-binding capacity of tau, destabilizes microtubules and may enhance the formation of paired helical filaments that constitute neurofibrillary tangles in Alzheimer's disease. Here, we use phosphorylation-dependent anti-tau antibodies to detect specific epitopes that characterize hyperphosphorylated tau. Our demonstration of intracellular tangles containing full-length tau that are not immunolabeled by these antibodies suggests that hyperphosphorylation of tau is not obligatory in the formation of neurofibrillary tangles in Alzheimer's disease.
成体人类神经细胞含有tau蛋白,一种磷酸化的微管相关蛋白,其在胎儿及阿尔茨海默病患者体内会发生过度磷酸化。过度磷酸化会降低tau蛋白与微管的结合能力,使微管不稳定,并可能增强成对螺旋丝的形成,而成对螺旋丝在阿尔茨海默病中构成神经原纤维缠结。在此,我们使用依赖磷酸化的抗tau抗体来检测表征过度磷酸化tau的特定表位。我们证明,含有全长tau的细胞内缠结未被这些抗体免疫标记,这表明在阿尔茨海默病神经原纤维缠结的形成过程中,tau的过度磷酸化并非必需。