Götz J, Probst A, Spillantini M G, Schäfer T, Jakes R, Bürki K, Goedert M
Preclinical Research, Sandoz Pharma Ltd, Basel, Switzerland.
EMBO J. 1995 Apr 3;14(7):1304-13. doi: 10.1002/j.1460-2075.1995.tb07116.x.
Microtubule-associated protein tau is the major constituent of the paired helical filament, the main fibrous component of the neurofibrillary lesions of Alzheimer's disease. Tau is an axonal phosphoprotein in normal adult brain. In Alzheimer's disease brain tau is hyperphosphorylated and is found not only in axons, but also in cell bodies and dendrites of affected nerve cells. We report the production and analysis of transgenic mice that express the longest human brain tau isoform under the control of the human Thy-1 promoter. As in Alzheimer's disease, transgenic human tau protein was present in nerve cell bodies, axons and dendrites; moreover, it was phosphorylated at sites that are hyperphosphorylated in paired helical filaments. We conclude that transgenic human tau protein showed pre-tangle changes similar to those that precede the full neurofibrillary pathology in Alzheimer's disease.
微管相关蛋白tau是成对螺旋丝的主要成分,而成对螺旋丝是阿尔茨海默病神经原纤维病变的主要纤维成分。Tau在正常成人大脑中是一种轴突磷蛋白。在阿尔茨海默病大脑中,tau发生了过度磷酸化,不仅存在于轴突中,还存在于受影响神经细胞的细胞体和树突中。我们报道了在人Thy-1启动子控制下表达最长人脑tau异构体的转基因小鼠的产生和分析。与阿尔茨海默病一样,转基因人tau蛋白存在于神经细胞体、轴突和树突中;此外,它在成对螺旋丝中过度磷酸化的位点发生了磷酸化。我们得出结论,转基因人tau蛋白显示出类似于阿尔茨海默病完全神经原纤维病理之前的缠结前变化。