组成型Dyrk1A在阿尔茨海默病、唐氏综合征、皮克病及相关转基因模型中异常表达。
Constitutive Dyrk1A is abnormally expressed in Alzheimer disease, Down syndrome, Pick disease, and related transgenic models.
作者信息
Ferrer Isidro, Barrachina Marta, Puig Berta, Martínez de Lagrán M, Martí Eulalia, Avila Jesús, Dierssen Mara
机构信息
Institut de Neuropatologia, Servei Anatomia Patològica, Hospital Universitari de Bellvitge, carrer Feixa Llarga sn, 08907 Hospitalet de Llobregat, Spain.
出版信息
Neurobiol Dis. 2005 Nov;20(2):392-400. doi: 10.1016/j.nbd.2005.03.020.
DYRK1A, dual-specificity tyrosine-regulated kinase 1A, maps to human chromosome 21 within the Down syndrome (DS) critical region. Dyrk1 phosphorylates the human microtubule-associated protein tau at Thr212 in vitro, a residue that is phosphorylated in fetal tau and hyper-phosphorylated in Alzheimer disease (AD) and tauopathies, including Pick disease (PiD). Furthermore, phosphorylation of Thr212 primes tau for phosphorylation by glycogen synthase kinase 3 (GSK-3). The present study examines Dyrk1A in the cerebral cortex of sporadic AD, adult DS with associated AD, and PiD. Increased Dyrk1A immunoreactivity has been found in the cytoplasm and nuclei of scattered neurons of the neocortex, entorhinal cortex, and hippocampus in AD, DS, and PiD. Dyrk1A is found in sarkosyl-insoluble fractions which are enriched in phosphorylated tau in AD brains, thus suggesting a possible association of Dyrk1A with neurofibrillary tangle pathology. Yet, no clear relationship has been observed between tau phosphorylation at Thr212, and GSK-3 and Dyrk1A expression in diseased brains. Transgenic mice bearing a triple tau mutation (G272V, P301L, and R406W) and expressing hyper-phosphoyrylated tau in neurons of the entorhinal cortex, hippocampus, and cerebral neocortex show increased expression of Dyrk1A in individual neurons in the same regions. However, transgenic mice over-expressing Dyrk1A do not show increased phosphorylation of tau at Thr212, thus suggesting that Dyrk1A over-expression does not trigger per se hyper-phosphorylation of tau at Thr212 in vivo. The present observations indicate modifications in the expression of constitutive Dyrk1A in the cytoplasm and nuclei of neurons in various neurodegenerative diseases associated with tau phosphorylation.
双重特异性酪氨酸调节激酶1A(DYRK1A)定位于人类21号染色体上的唐氏综合征(DS)关键区域内。Dyrk1在体外可使人类微管相关蛋白tau在苏氨酸212位点发生磷酸化,该位点在胎儿tau蛋白中被磷酸化,而在阿尔茨海默病(AD)及包括Pick病(PiD)在内的tau蛋白病中则发生过度磷酸化。此外,苏氨酸212位点的磷酸化会促使tau蛋白被糖原合酶激酶3(GSK-3)磷酸化。本研究对散发性AD、伴有相关AD的成年DS患者以及PiD患者大脑皮质中的Dyrk1A进行了检测。在AD、DS和PiD患者的新皮质、内嗅皮质和海马体中,散在神经元的细胞质和细胞核内发现Dyrk1A免疫反应性增强。在AD脑内富含磷酸化tau蛋白的 Sarkosyl不溶性组分中发现了Dyrk1A,这表明Dyrk1A可能与神经原纤维缠结病理改变有关。然而,在患病大脑中,未观察到苏氨酸212位点的tau蛋白磷酸化与GSK-3及Dyrk1A表达之间存在明确的关系。携带三重tau突变(G272V、P301L和R406W)并在内嗅皮质、海马体和大脑新皮质神经元中表达过度磷酸化tau蛋白的转基因小鼠,在相同区域的单个神经元中显示出Dyrk1A表达增加。然而,过度表达Dyrk1A的转基因小鼠并未显示出苏氨酸212位点的tau蛋白磷酸化增加,这表明在体内Dyrk1A的过度表达本身并不会引发苏氨酸212位点的tau蛋白过度磷酸化。目前的观察结果表明,在与tau蛋白磷酸化相关的各种神经退行性疾病中,神经元细胞质和细胞核内组成型Dyrk1A的表达发生了改变。