Literature DB >> 25520289

Modeling Axonal Phenotypes with Human Pluripotent Stem Cells.

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.

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Keywords:  Axon; Degeneration; Mitochondria; hESCs; iPSCs

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Year:  2016        PMID: 25520289     DOI: 10.1007/7651_2014_167

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia.

Authors:  Yongchao Mou; Sukhada Mukte; Eric Chai; Joshua Dein; Xue-Jun Li
Journal:  J Vis Exp       Date:  2020-02-09       Impact factor: 1.355

2.  Monitoring Axonal Degeneration in Human Pluripotent Stem Cell Models of Hereditary Spastic Paraplegias.

Authors:  Xue-Jun Li; Yongchao Mou; Conrad Milton; Zhenyu Chen
Journal:  Methods Mol Biol       Date:  2022

3.  Drug screening with human SMN2 reporter identifies SMN protein stabilizers to correct SMA pathology.

Authors:  Yiran Wang; Chongchong Xu; Lin Ma; Yongchao Mou; Bowen Zhang; Shanshan Zhou; Yue Tian; Jessica Trinh; Xiaoqing Zhang; Xue-Jun Li
Journal:  Life Sci Alliance       Date:  2019-03-25
  3 in total

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