| Literature DB >> 35659876 |
Lucia S Capano1, Chihiro Sato2, Elena Ficulle3, Anan Yu4, Kanta Horie2, Ji-Sun Kwon5, Kyle F Burbach6, Nicolas R Barthélemy2, Susan G Fox4, Celeste M Karch7, Randall J Bateman8, Henry Houlden3, Richard I Morimoto4, David M Holtzman8, Karen E Duff9, Andrew S Yoo10.
Abstract
Tau is a microtubule-binding protein expressed in neurons, and the equal ratios between 4-repeat (4R) and 3-repeat (3R) isoforms are maintained in normal adult brain function. Dysregulation of 3R:4R ratio causes tauopathy, and human neurons that recapitulate tau isoforms in health and disease will provide a platform for elucidating pathogenic processes involving tau pathology. We carried out extensive characterizations of tau isoforms expressed in human neurons derived by microRNA-induced neuronal reprogramming of adult fibroblasts. Transcript and protein analyses showed that miR neurons expressed all six isoforms with the 3R:4R isoform ratio equivalent to that detected in human adult brains. Also, miR neurons derived from familial tauopathy patients with a 3R:4R ratio altering mutation showed increased 4R tau and the formation of insoluble tau with seeding activity. Our results collectively demonstrate the utility of miRNA-induced neuronal reprogramming to recapitulate endogenous tau regulation comparable with the adult brain in health and disease.Entities:
Keywords: 4R tau; adult human neurons; insoluble tau; microRNA-induced neurons; neuronal reprogramming; tau isoform ratio; tau isoforms; tau seeding; tauopathy
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Year: 2022 PMID: 35659876 PMCID: PMC9176216 DOI: 10.1016/j.stem.2022.04.018
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269