Combinatorial model of amyloid β and tau reveals synergy between amyloid deposits and tangle formation. (10th December 2021)

• Record Type: Journal Article
• Authors: Koller, Emily J.; Ibanez, Kristen R.; Vo, Quan; McFarland, Karen N.; Gonzalez De La Cruz, Elsa; Zobel, Lillian; Williams, Tristan; Xu, Guilian; Ryu, Daniel; Patel, Preya; Giasson, Benoit I.; Prokop, Stefan; Chakrabarty, Paramita
• Is Part Of: Neuropathology & applied neurobiology. Volume 48:Number 2(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-12-10
• Subjects: Alzheimer's disease -- gliosis -- neurofibrillary tangle -- neuroinflammation -- pathological synergy -- plaque burden; Nervous system -- Diseases -- Pathology -- Periodicals; Nervous system -- Diseases -- Periodicals; 616.8
• DOI: 10.1111/nan.12779
• Languages: English
• ISSNs: 0305-1846

Abstract

Abstract: Aims: To illuminate the pathological synergy between Aβ and tau leading to emergence of neurofibrillary tangles (NFT) in Alzheimer's disease (AD), here, we have performed a comparative neuropathological study utilising three distinctive variants of human tau (WT tau, P301L mutant tau and S320F mutant tau). Previously, in non‐transgenic mice, we showed that WT tau or P301L tau does not form NFT while S320F tau can spontaneously aggregate into NFT, allowing us to test the selective vulnerability of these different tau conformations to the presence of Aβ plaques. Methods: We injected recombinant AAV‐tau constructs into neonatal APP transgenic TgCRND8 mice or into 3‐month‐old TgCRND8 mice; both cohorts were aged 3 months post injection. This allowed us to test how different tau variants synergise with soluble forms of Aβ (pre‐deposit cohort) or with frank Aβ deposits (post‐deposit cohort). Results: Expression of WT tau did not produce NFT or altered Aβ in either cohort. In the pre‐deposit cohort, S320F tau induced Aβ plaque deposition, neuroinflammation and synaptic abnormalities, suggesting that early tau tangles affect the amyloid cascade. In the post‐deposit cohort, contemporaneous expression of S320F tau did not exacerbate amyloid pathology, showing a dichotomy in Aβ‐tau synergy based on the nature of Aβ. P301L tau produced NFT‐type inclusions in the post‐deposit cohort, but not in the pre‐deposit cohort, indicating pathological synergy with pre‐existing Aβ deposits. Conclusions: Our data show that different tau mutations representing specific folding variants of tau synergise with Aβ to different extents, depending on the presence of cerebral deposits. Abstract : Koller and colleagues examine the apparent synergy between amyloid β (Aβ) and tau leading to formation of Alzheimer‐typical pathological tau inclusions. Following expression of different tau variants, their study reveals that different tau mutants synergize with Aβ to different extents, depending on the presence of cerebral Aβ deposits. They further report that contemporaneous expression of P301L mutant human tau, but not wild type human tau, accelerates emergence of hippocampal tau inclusions in the presence of Aβ deposits.