Togo Takashi, Akiyama Haruhiko, Iseki Eizo, Uchikado Hirotake, Kondo Hiromi, Ikeda Kenji, Tsuchiya Kuniaki, de Silva Rohan, Lees Andrew, Kosaka Kenji
Tokyo Institute of Psychiatry, 2-1-8 Kamikitazawa, Setagaya-ku, 156-8585 Tokyo, Japan.
Acta Neuropathol. 2004 Jun;107(6):504-8. doi: 10.1007/s00401-004-0842-2. Epub 2004 Mar 16.
Accumulation of abnormally phosphorylated tau results in the formation of neurofibrillary tangles (NFTs) in the neuronal cell soma and neuropil threads (NTs) in the cell processes. In the present study, we used immunohistochemistry to investigate serially cut thick tissue sections from the brains of patients with Alzheimer's disease (AD) and non-demented elderly subjects. In the early stages of neurofibrillary pathology, clusters of NTs occurred occasionally in the cerebral cortex. Each NTs cluster, the entire extent of which was observed in the serial sections, corresponded to a dendritic tree that was arborized from a tau-positive neuron. Adult human brain contains six tau isoforms with three having three carboxyl-terminal tandem repeat sequences that are encoded by exon 10 (3R-tau) and the other three having four repeat sequences (4R-tau). Three isoform patterns, 3R-tau(+)/4R-tau(-), 3R-tau(-)/4R-tau(+) and 3R-tau(+)/4R-tau(+), were seen in NFTs in early stage AD lesions. In an individual neuron, the isoform pattern was consistent between the NFTs in the cell soma and the NTs in the cell processes. The results of this study indicate that, in early stages of AD and age-associated neurofibrillary changes, tau accumulates simultaneously in the cell soma and cell processes of affected neurons. The process of AD and age-associated tau pathology is not tau-isoform-specific, but the ratio of 3R-tau and 4R-tau isoforms involved in the neurofibrillary changes varies and is specific to individual neurons.
异常磷酸化的tau蛋白积累会导致神经元细胞体中形成神经原纤维缠结(NFTs)以及细胞突起中形成神经丝(NTs)。在本研究中,我们使用免疫组织化学方法对阿尔茨海默病(AD)患者和非痴呆老年受试者大脑的连续厚组织切片进行了研究。在神经原纤维病变的早期阶段,NTs簇偶尔出现在大脑皮层中。每个NTs簇在连续切片中都能观察到其完整范围,对应于一个从tau阳性神经元发出分支的树突树。成人大脑中含有六种tau异构体,其中三种具有由外显子10编码的三个羧基末端串联重复序列(3R-tau),另外三种具有四个重复序列(4R-tau)。在早期AD病变的NFTs中可见三种异构体模式,即3R-tau(+)/4R-tau(-)、3R-tau(-)/4R-tau(+)和3R-tau(+)/4R-tau(+)。在单个神经元中,细胞体中的NFTs和细胞突起中的NTs之间的异构体模式是一致的。本研究结果表明,在AD和与年龄相关的神经原纤维变化的早期阶段,tau蛋白在受影响神经元的细胞体和细胞突起中同时积累。AD和与年龄相关的tau病理过程并非tau异构体特异性的,但参与神经原纤维变化的3R-tau和4R-tau异构体的比例各不相同,且因单个神经元而异。