CSF tau microtubule binding region identifies tau tangle and clinical stages of Alzheimer's disease

被引:102
作者
Horie, Kanta [1 ]
Barthelemy, Nicolas R. [1 ]
Sato, Chihiro [1 ]
Bateman, Randall J. [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol, BJC Inst Hlth 9603,425 South Euclid Ave, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
[3] Washington Univ, Charles F & Joanne Knight Alzheimers Dis Res Ctr, Sch Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
CSF; biomarkers; tau; microtubule binding region; Alzheimer's disease; CEREBROSPINAL-FLUID; NEUROFIBRILLARY TANGLES; MASS-SPECTROMETRY; CASPASE CLEAVAGE; PATHOLOGY; PROPAGATION; TAUOPATHIES; PROTEIN; FRAGMENTS; SEQUENCE;
D O I
10.1093/brain/awaa373
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tau is a microtubule associated protein in the brain that aggregates in Alzheimer's disease to form pathological tangles and neurites. Insoluble tau aggregates composed of the microtubule binding region (MTBR) of tau are highly associated with the cognitive and clinical symptoms of Alzheimer's disease. In contrast, levels of soluble forms of tau, such as CSF total tau and phosphorylated tau-181 and tau-217, increase prior to tau aggregation in Alzheimer's disease, but these biomarkers do not measure the MTBR of tau. Thus, how CSF MTBR-tau is altered in Alzheimer's disease remains unclear. In this study, we used sequential immunoprecipitation and chemical extraction methods followed by mass spectrometry to analyse MTBR-tau species in Alzheimer's disease and control CSF. We quantified MTBR-tau-specific regions in the CSF and identified that species containing the region beginning at residue 243 were the most highly correlated with tau PET and cognitive measures. This finding suggests that CSF level of tau species containing the upstream region of MTBR may reflect changes in tau pathology that occur in Alzheimer's disease and could serve as biomarkers to stage Alzheimer's disease and track the development of tau-directed therapeutics.
引用
收藏
页码:515 / 527
页数:13
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