| Literature DB >> 26068894 |
Young Hye Kim1, Se Hoon Choi2, Carla D'Avanzo2, Matthias Hebisch3, Christopher Sliwinski2, Enjana Bylykbashi2, Kevin J Washicosky2, Justin B Klee2, Oliver Brüstle4, Rudolph E Tanzi2, Doo Yeon Kim2.
Abstract
Stem cell technologies have facilitated the development of human cellular disease models that can be used to study pathogenesis and test therapeutic candidates. These models hold promise for complex neurological diseases such as Alzheimer's disease (AD), because existing animal models have been unable to fully recapitulate all aspects of pathology. We recently reported the characterization of a novel 3D culture system that exhibits key events in AD pathogenesis, including extracellular aggregation of amyloid-β (Aβ) and accumulation of hyperphosphorylated tau. Here we provide instructions for the generation and analysis of 3D human neural cell cultures, including the production of genetically modified human neural progenitor cells (hNPCs) with familial AD mutations, the differentiation of the hNPCs in a 3D matrix and the analysis of AD pathogenesis. The 3D culture generation takes 1-2 d. The aggregation of Aβ is observed after 6 weeks of differentiation, followed by robust tau pathology after 10-14 weeks.Entities:
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Year: 2015 PMID: 26068894 PMCID: PMC4499058 DOI: 10.1038/nprot.2015.065
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491