Literature DB >> 25273538

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

David J Brick1, Hubert E Nethercott1, Samantha Montesano1, Maria G Banuelos1, Alexander E Stover1, Soleil Sun Schutte1, Diane K O'Dowd1, Randi J Hagerman1, Michele Ono1, David R Hessl1, Flora Tassone1, Philip H Schwartz2.   

Abstract

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 all lines available on request with the goal of advancing the use of ASD patient cells as disease models by the scientific community. ©AlphaMed Press.

Entities:  

Keywords:  Autism spectrum disorder; Differentiation; Disease modeling; Induced pluripotent stem cells; Neural stem cell; Neuron

Mesh:

Year:  2014        PMID: 25273538      PMCID: PMC4214842          DOI: 10.5966/sctm.2014-0073

Source DB:  PubMed          Journal:  Stem Cells Transl Med        ISSN: 2157-6564            Impact factor:   6.940


  67 in total

1.  Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome.

Authors:  F Tassone; R J Hagerman; D Garcia-Arocena; E W Khandjian; C M Greco; P J Hagerman
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

2.  Astrocytes prevent abnormal neuronal development in the fragile x mouse.

Authors:  Shelley Jacobs; Laurie C Doering
Journal:  J Neurosci       Date:  2010-03-24       Impact factor: 6.167

3.  Derivation of induced pluripotent stem cells by lentiviral transduction.

Authors:  Hubert E Nethercott; David J Brick; Philip H Schwartz
Journal:  Methods Mol Biol       Date:  2011

4.  Modeling an autism risk factor in mice leads to permanent immune dysregulation.

Authors:  Elaine Y Hsiao; Sara W McBride; Janet Chow; Sarkis K Mazmanian; Paul H Patterson
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-16       Impact factor: 11.205

Review 5.  Disentangling the heterogeneity of autism spectrum disorder through genetic findings.

Authors:  Shafali S Jeste; Daniel H Geschwind
Journal:  Nat Rev Neurol       Date:  2014-01-28       Impact factor: 42.937

6.  Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.

Authors:  T A Comery; J B Harris; P J Willems; B A Oostra; S A Irwin; I J Weiler; W T Greenough
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-13       Impact factor: 11.205

7.  The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Authors:  C Lord; S Risi; L Lambrecht; E H Cook; B L Leventhal; P C DiLavore; A Pickles; M Rutter
Journal:  J Autism Dev Disord       Date:  2000-06

8.  Generation of human-induced pluripotent stem cells.

Authors:  In-Hyun Park; Paul H Lerou; Rui Zhao; Hongguang Huo; George Q Daley
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

Review 9.  A synaptic trek to autism.

Authors:  Thomas Bourgeron
Journal:  Curr Opin Neurobiol       Date:  2009-06-21       Impact factor: 6.627

10.  Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs.

Authors:  Gabsang Lee; Eirini P Papapetrou; Hyesoo Kim; Stuart M Chambers; Mark J Tomishima; Christopher A Fasano; Yosif M Ganat; Jayanthi Menon; Fumiko Shimizu; Agnes Viale; Viviane Tabar; Michel Sadelain; Lorenz Studer
Journal:  Nature       Date:  2009-08-19       Impact factor: 49.962

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  12 in total

1.  The fragile X mutation impairs homeostatic plasticity in human neurons by blocking synaptic retinoic acid signaling.

Authors:  Zhenjie Zhang; Samuele G Marro; Yingsha Zhang; Kristin L Arendt; Christopher Patzke; Bo Zhou; Tyler Fair; Nan Yang; Thomas C Südhof; Marius Wernig; Lu Chen
Journal:  Sci Transl Med       Date:  2018-08-01       Impact factor: 17.956

2.  Culturing Human Pluripotent and Neural Stem Cells in an Enclosed Cell Culture System for Basic and Preclinical Research.

Authors:  Alexander E Stover; Siranush Herculian; Maria G Banuelos; Samantha L Navarro; Michael P Jenkins; Philip H Schwartz
Journal:  J Vis Exp       Date:  2016-06-10       Impact factor: 1.355

Review 3.  Human pluripotent stem cell models of Fragile X syndrome.

Authors:  Anita Bhattacharyya; Xinyu Zhao
Journal:  Mol Cell Neurosci       Date:  2015-11-27       Impact factor: 4.314

4.  Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene.

Authors:  X Shawn Liu; Hao Wu; Marine Krzisch; Xuebing Wu; John Graef; Julien Muffat; Denes Hnisz; Charles H Li; Bingbing Yuan; Chuanyun Xu; Yun Li; Dan Vershkov; Angela Cacace; Richard A Young; Rudolf Jaenisch
Journal:  Cell       Date:  2018-02-15       Impact factor: 41.582

5.  Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells.

Authors:  Meng Li; Huashan Zhao; Gene E Ananiev; Michael T Musser; Kathryn H Ness; Dianne L Maglaque; Krishanu Saha; Anita Bhattacharyya; Xinyu Zhao
Journal:  Stem Cells       Date:  2016-07-27       Impact factor: 6.277

Review 6.  Patient-derived iPSC modeling of rare neurodevelopmental disorders: Molecular pathophysiology and prospective therapies.

Authors:  K R Sabitha; Ashok K Shetty; Dinesh Upadhya
Journal:  Neurosci Biobehav Rev       Date:  2020-12-25       Impact factor: 8.989

Review 7.  Bio-collections in autism research.

Authors:  Jamie Reilly; Louise Gallagher; June L Chen; Geraldine Leader; Sanbing Shen
Journal:  Mol Autism       Date:  2017-07-10       Impact factor: 7.509

8.  Reproducible and efficient generation of functionally active neurons from human hiPSCs for preclinical disease modeling.

Authors:  Yunyao Xie; Ryan J Schutte; Nathan N Ng; Kevin C Ess; Philip H Schwartz; Diane K O'Dowd
Journal:  Stem Cell Res       Date:  2017-12-09       Impact factor: 2.020

Review 9.  A Dishful of a Troubled Mind: Induced Pluripotent Stem Cells in Psychiatric Research.

Authors:  Sára Kálmán; Edit Hathy; János M Réthelyi
Journal:  Stem Cells Int       Date:  2015-12-29       Impact factor: 5.443

Review 10.  Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.

Authors:  Hagar Mor-Shaked; Rachel Eiges
Journal:  Genes (Basel)       Date:  2016-09-28       Impact factor: 4.096

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