The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery

被引:26
作者
Brick, David J. [1 ,2 ]
Nethercott, Hubert E. [1 ,2 ]
Montesano, Samantha [1 ,2 ]
Banuelos, Maria G. [1 ,2 ]
Stover, Alexander E. [1 ,2 ]
Schutte, Soleil Sun [3 ]
O'Dowd, Diane K. [3 ]
Hagerman, Rand J. [4 ,5 ]
Ono, Michele [4 ,5 ]
Hessl, David R. [4 ,5 ]
Tassone, Flora [4 ,6 ]
Schwartz, Philip H. [1 ,2 ]
机构
[1] Childrens Hosp, Cty Res Inst, Ctr Neurosci, Orange, CA 92868 USA
[2] Childrens Hosp, Cty Res Inst, Ctr Translat Res, Orange, CA 92868 USA
[3] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92717 USA
[4] Univ Calif Davis, MIND Inst, Davis, CA 95616 USA
[5] Univ Calif Davis, Dept Pediat, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Biochem & Mol Med, Davis, CA 95616 USA
关键词
Induced pluripotent stem cells; Neural stem cell; Neuron; Disease modeling; Differentiation; Autism spectrum disorder; DE-NOVO MUTATIONS; NEURAL PROGENITOR CELLS; FRAGILE-X-SYNDROME; TREMOR/ATAXIA SYNDROME; INTRANUCLEAR INCLUSIONS; NEURONAL DEVELOPMENT; EXPANDED ALLELES; FMR1; GENE; PREMUTATION; DIFFERENTIATION;
D O I
10.5966/sctm.2014-0073
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The autism spectrum disorders (ASDs) comprise a set of neurodevelopmental disorders that are, at best, poorly understood but are the fastest growing developmental disorders in the United States. Because animal models of polygenic disorders such as the ASDs are difficult to validate, the derivation of induced pluripotent stem cells (iPSCs) by somatic cell reprogramming offers an alternative strategy for identifying the cellular mechanisms contributing to ASDs and the development of new treatment " options. Access to statistically relevant numbers of ASD patient cell lines, however, is still a limiting factor for the field. We describe a new resource with more than 200 cell lines (fibroblasts, iPSC clones, neural stem cells, glia) from unaffected volunteers and patients with a wide range of clinical ASD diagnoses, including fragile X syndrome. We have shown that both normal and ASD-specific iPSCs can be differentiated toward a neural stem cell phenotype and terminally differentiated into action-potential firing neurons and glia. The ability to evaluate and compare data from a number of different cell lines will facilitate greater insight into the cause or causes and biology of the ASDs and will be extremely useful for uncovering new therapeutic and diagnostic targets. Some drug treatments have already shown promise in reversing the neurobiological abnormalities in iPSC-based models of ASD-associated diseases. The ASD Stem Cell Resource at the Children's Hospital of Orange County will continue expanding its collection and make Wines available on request with the goal of advancing the use of ASD patient cells as disease models by the scientific community.
引用
收藏
页码:1275 / 1286
页数:12
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