| Literature DB >> 25520289 |
Kyle R Denton1, Chong-Chong Xu1, Xue-Jun Li2,3.
Abstract
Impaired axonal development and degeneration are implicated in many debilitating disorders, such as hereditary spastic paraplegia (HSP), amyotrophic lateral sclerosis (ALS), and periphery neuropathy. Human pluripotent stem cells (hPSCs) have provided researchers with an excellent resource for modeling human neuropathologic processes including axonal defects in vitro. There are a number of steps that are crucial when developing an hPSC-based model of a human disease, including generating induced pluripotent stem cells (iPSCs), differentiating those cells to affected cell types, and identifying disease-relevant phenotypes. Here, we describe these steps in detail, focusing on the neurodegenerative disorder HSP.Entities:
Keywords: Axon; Degeneration; Mitochondria; hESCs; iPSCs
Mesh:
Substances:
Year: 2016 PMID: 25520289 DOI: 10.1007/7651_2014_167
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745