| Literature DB >> 26260244 |
Eleonora Passeri1, Ashley M Wilson1, Amedeo Primerano1, Mari A Kondo1, Srona Sengupta1, Rupali Srivastava1, Minori Koga1, Cassandra Obie2, Peter P Zandi3, Fernando S Goes1, David Valle2, Judith L Rapoport4, Akira Sawa5, Shin-ichi Kano6, Koko Ishizuka7.
Abstract
The novel technology of induced neuronal cells (iN cells) is promising for translational neuroscience, as it allows the conversion of human fibroblasts into cells with postmitotic neuronal traits. However, a major technical barrier is the low conversion rate. To overcome this problem, we optimized the conversion media. Using our improved formulation, we studied how major mental illness-associated chromosomal abnormalities may impact the characteristics of iN cells. We demonstrated that our new iN cell culture protocol enabled us to obtain more precise measurement of neuronal cellular phenotypes than previous iN cell methods. Thus, this iN cell culture provides a platform to efficiently obtain possible cellular phenotypes caused by genetic differences, which can be more thoroughly studied in research using other human cell models such as induced pluripotent stem cells.Entities:
Keywords: Childhood-onset schizophrenia; Conversion rate; Copy number variations (CNVs); Fibroblasts; Process length; Schizophrenia; Translational research; iN cells
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Year: 2015 PMID: 26260244 PMCID: PMC4774521 DOI: 10.1016/j.neures.2015.07.011
Source DB: PubMed Journal: Neurosci Res ISSN: 0168-0102 Impact factor: 3.304