Liu W K, Williams R T, Hall F L, Dickson D W, Yen S H
Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461.
Am J Pathol. 1995 Jan;146(1):228-38.
By immunocytochemical staining and Western blotting, we detected a Cdc2-related kinase in human brains. The kinase is recognized by antibodies against the carboxyl and the amino termini of p34Cdc2 but is not recognized by antibodies against the PSTAIRE motif. It is slightly smaller than p34Cdc2 in molecular mass (approximately 33 kd). This 33-kd Cdc2-related kinase is present in intracellular neurofibrillary tangles in neurons of elderly humans and in Alzheimer's disease, and it is associated with paired helical filaments (PHF) from Alzheimer's disease brains. Unlike the antibodies to the carboxyl and amino termini of p34Cdc2, antibodies to an abundant brain Cdc2-related kinase PSSLARE/Cdk5 did not immunolabel Alzheimer's disease neurofibrillary lesions. PHF preparations were demonstrated to contain kinases capable of phosphorylating histone H1, PHF-Tau, and a synthetic peptide (VAVVRTPPKSPSSAK). By virtue of its physical association with PHF, the 33-kd Cdc2-related kinase may play a role in transforming normal Tau proteins to PHF-Tau characteristic of Alzheimer's disease.
通过免疫细胞化学染色和蛋白质印迹法,我们在人脑中检测到一种与Cdc2相关的激酶。该激酶可被抗p34Cdc2羧基末端和氨基末端的抗体识别,但不能被抗PSTAIRE基序的抗体识别。其分子量略小于p34Cdc2(约33kd)。这种33kd的与Cdc2相关的激酶存在于老年人和阿尔茨海默病患者神经元的细胞内神经原纤维缠结中,并且与阿尔茨海默病大脑中的双螺旋丝(PHF)相关。与抗p34Cdc2羧基末端和氨基末端的抗体不同,抗一种丰富的脑Cdc2相关激酶PSSLARE/Cdk5的抗体不能对阿尔茨海默病神经原纤维病变进行免疫标记。PHF制剂被证明含有能够磷酸化组蛋白H1、PHF-Tau和一种合成肽(VAVVRTPPKSPSSAK)的激酶。由于其与PHF的物理关联,这种33kd的与Cdc2相关的激酶可能在将正常Tau蛋白转化为阿尔茨海默病特有的PHF-Tau过程中发挥作用。