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

Author:

Horie Kanta1ORCID,Barthélemy Nicolas R1,Sato Chihiro1,Bateman Randall J123

Affiliation:

1. Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA

2. Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO, USA

3. Charles F. and Joanne Knight Alzheimer’s Disease Research Center, Washington University School of Medicine, St. Louis, MO, USA

Abstract

Abstract 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.

Funder

National Institutes of Health (NIH) National Institute of Neurological Disorders and Stroke

Foundation for Barnes-Jewish Hospital

John and Linda Tracy Family

Coins for Alzheimer’s Research Trust

Alzheimer’s Association Research Fellowship

NIH

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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