A peptide inhibitor of Tau-SH3 interactions ameliorates amyloid-β toxicity

NEUROBIOLOGY OF DISEASE

卷:134

Article

Rush, Travis ; Roth, Jonathan R. ; Thompson, Samantha J. ; Aldaher, Adam R. ; Cochran, J. Nicholas ; Roberson, Erik D.

关键词: Amyloid-beta;    Oligomer;    Tau;    SH3;    Fyn;    Alzheimer's disease;   

DOI  :  10.1016/j.nbd.2019.104668

来源: Elsevier

【 摘 要 】

The microtubule-associated protein Tau is strongly implicated in Alzheimer's disease (AD) and aggregates into neurofibrillary tangles in AD. Genetic reduction of Tau is protective in several animal models of AD and cell culture models of amyloid-beta (A beta) toxicity, making it an exciting therapeutic target for treating AD. A variety of evidence indicates that Tau's interactions with Fyn kinase and other SH3 domain-containing proteins, which bind to PxxP motifs in Tau's proline-rich domain, may contribute to AD deficits and A beta toxicity. Thus, we sought to determine if inhibiting Tau-SH3 interactions ameliorates A beta toxicity. We developed a peptide inhibitor of Tau-SH3 interactions and a proximity ligation assay (PLA)-based target engagement assay. Then, we used membrane trafficking and neurite degeneration assays to determine if inhibiting Tau-SH3 interactions ameliorated A beta oligomer (A beta o)-induced toxicity in primary hippocampal neurons from rats. We verified that Tau reduction ameliorated A beta o toxicity in neurons. Using PLA, we identified a peptide inhibitor that reduced Tau-SH3 interactions in HEK-293 cells and primary neurons. This peptide reduced Tau phosphorylation by Fyn without affecting Fyn's kinase activity state. In primary neurons, endogenous Tau-Fyn interaction was present primarily in neurites and was reduced by the peptide inhibitor, from which we inferred target engagement. Reducing Tau-SH3 interactions in neurons ameliorated A beta o toxicity by multiple outcome measures, namely A beta o-induced membrane trafficking abnormalities and neurite degeneration. Our results indicate that Tau-SH3 interactions are critical for A beta o toxicity and that inhibiting them is a promising therapeutic target for AD.