ELISA Evaluation of Tau Accumulation in the Brains of Patients with Alzheimer Disease. Issue 7 (20th July 2021)

• Record Type: Journal Article
• Authors: Shinohara, Mitsuru; Hirokawa, Junko; Shimodaira, Akemi; Tashiro, Yoshitaka; Suzuki, Kaoru; Gheni, Ghupurjan; Fukumori, Akio; Matsubara, Tomoyasu; Morishima, Maho; Saito, Yuko; Murayama, Shigeo; Sato, Naoyuki
• Is Part Of: Journal of neuropathology and experimental neurology. Volume 80:Issue 7(2021)
• Page Start: 652
• Page End: 662
• Publication Date: 2021-07-20
• Subjects: Alzheimer disease -- Brain -- Enzyme-linked immunosorbent assay (ELISA) -- Tau; Neurology -- Diseases -- Periodicals; Neurology -- Diseases -- Physiopathology -- Periodicals; 616.8047
• DOI: 10.1093/jnen/nlab047
• Languages: English
• ISSNs: 0022-3069

Abstract

Abstract: Despite the routine use of sandwich enzyme-linked immunosorbent assays (ELISAs) for quantifying tau levels in CSF and plasma, tau accumulations in the brains of patients with Alzheimer disease (AD) have rarely been evaluated by this method. Thus, by introducing several tau ELISAs that target different epitopes, we evaluated accumulated tau levels in postmortem brains depending on disease stage, brain areas, and other AD-related changes. Notably, tau levels in insoluble fraction determined by each ELISAs differ depending on the epitopes of antibodies: non-AD control samples yield relatively high signals when an antibody against the N-terminal region of tau is used. On the other hand, ELISAs combining antibodies against the later-middle to C-terminal regions of tau produced substantially increased signals from AD samples, compared to those from non-AD controls. Such ELISAs better distinguish AD and non-AD controls, and the results are more closely associated with Braak neurofibrillary tangles stage, Aβ accumulation, and glial markers. Moreover, these ELISAs can reflect the pattern of tau spread across brain regions. In conclusion, Tau ELISAs that combine antibodies against the later-middle to C-terminal regions of tau can better reflect neuropathological tau accumulation, which would enable to evaluate tau accumulation in the brain at a biochemical level.