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Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells
Down syndrome (DS, trisomy 21), is the most common viable chromosomal disorder, with an incidence of 1 in 800 live births. Its phenotypic characteristics include intellectual impairment and several other developmental abnormalities, for the majority of which the pathogenetic mechanisms remain unknow...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470162/ https://www.ncbi.nlm.nih.gov/pubmed/26239351 http://dx.doi.org/10.3390/jcm4040696 |
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author | Hibaoui, Youssef Feki, Anis |
author_facet | Hibaoui, Youssef Feki, Anis |
author_sort | Hibaoui, Youssef |
collection | PubMed |
description | Down syndrome (DS, trisomy 21), is the most common viable chromosomal disorder, with an incidence of 1 in 800 live births. Its phenotypic characteristics include intellectual impairment and several other developmental abnormalities, for the majority of which the pathogenetic mechanisms remain unknown. Several models have been used to investigate the mechanisms by which the extra copy of chromosome 21 leads to the DS phenotype. In the last five years, several laboratories have been successful in reprogramming patient cells carrying the trisomy 21 anomaly into induced pluripotent stem cells, i.e., T21-iPSCs. In this review, we summarize the different T21-iPSCs that have been generated with a particular interest in the technical procedures and the somatic cell types used for the reprogramming. |
format | Online Article Text |
id | pubmed-4470162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44701622015-07-28 Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells Hibaoui, Youssef Feki, Anis J Clin Med Review Down syndrome (DS, trisomy 21), is the most common viable chromosomal disorder, with an incidence of 1 in 800 live births. Its phenotypic characteristics include intellectual impairment and several other developmental abnormalities, for the majority of which the pathogenetic mechanisms remain unknown. Several models have been used to investigate the mechanisms by which the extra copy of chromosome 21 leads to the DS phenotype. In the last five years, several laboratories have been successful in reprogramming patient cells carrying the trisomy 21 anomaly into induced pluripotent stem cells, i.e., T21-iPSCs. In this review, we summarize the different T21-iPSCs that have been generated with a particular interest in the technical procedures and the somatic cell types used for the reprogramming. MDPI 2015-04-15 /pmc/articles/PMC4470162/ /pubmed/26239351 http://dx.doi.org/10.3390/jcm4040696 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hibaoui, Youssef Feki, Anis Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title | Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title_full | Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title_fullStr | Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title_full_unstemmed | Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title_short | Concise Review: Methods and Cell Types Used to Generate Down Syndrome Induced Pluripotent Stem Cells |
title_sort | concise review: methods and cell types used to generate down syndrome induced pluripotent stem cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470162/ https://www.ncbi.nlm.nih.gov/pubmed/26239351 http://dx.doi.org/10.3390/jcm4040696 |
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