Goedert M
Medical Research Council, Laboratory of Molecular Biology, Cambridge, UK.
Trends Neurosci. 1993 Nov;16(11):460-5. doi: 10.1016/0166-2236(93)90078-z.
Abundant neurofibrillary tangles, neuropil threads and senile plaque neurites constitute the neurofibrillary pathology of Alzheimer's disease. They form in the nerve cells that undergo degeneration in the disease, in which their regional distribution correlates with the degree of dementia. Each lesion contains the paired helical filament (PHF) as its major fibrous component. Recent work has shown that PHFs are composed of the microtubule-associated protein tau in an abnormally phosphorylated state. PHF-tau is hyperphosphorylated on all six adult brain isoforms. As a consequence, tau is unable to bind to microtubules and is believed to self-assemble into the PHF. Current evidence suggests that protein kinases or protein phosphatases with a specificity for serine/threonine-proline residues are involved in the abnormal phosphorylation of tau.
大量神经原纤维缠结、神经毡丝和老年斑神经突构成了阿尔茨海默病的神经原纤维病理特征。它们在该疾病中发生变性的神经细胞中形成,其区域分布与痴呆程度相关。每个病变都含有双螺旋丝(PHF)作为其主要纤维成分。最近的研究表明,PHF由异常磷酸化状态的微管相关蛋白tau组成。PHF-tau在所有六种成人大脑异构体上均过度磷酸化。因此,tau无法与微管结合,并被认为会自我组装成PHF。目前的证据表明,对丝氨酸/苏氨酸-脯氨酸残基具有特异性的蛋白激酶或蛋白磷酸酶参与了tau的异常磷酸化。