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Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects
Down syndrome is a congenital disorder resulting from an extra full or partial chromosome 21, which is characterized by a spectrum of systemic developmental abnormalities, including those affecting the cardiovascular system. Here, we generated an iPSC line from peripheral blood mononuclear cells of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578300/ https://www.ncbi.nlm.nih.gov/pubmed/37393719 http://dx.doi.org/10.1016/j.scr.2023.103156 |
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author | Alonzo, Matthew Ye, Shiqiao Beckman, Brian Texter, Karen Garg, Vidu Zhao, Ming-Tao |
author_facet | Alonzo, Matthew Ye, Shiqiao Beckman, Brian Texter, Karen Garg, Vidu Zhao, Ming-Tao |
author_sort | Alonzo, Matthew |
collection | PubMed |
description | Down syndrome is a congenital disorder resulting from an extra full or partial chromosome 21, which is characterized by a spectrum of systemic developmental abnormalities, including those affecting the cardiovascular system. Here, we generated an iPSC line from peripheral blood mononuclear cells of a male adolescent with Down syndrome-associated congenital heart defects through Sendai virus-mediated transfection of 4 Yamanaka factors. This line exhibited normal morphology, expressed pluripotency markers, trisomy 21 karyotype, and could be differentiated into three germ layers. This iPSC line can be used for studying cellular and developmental etiologies of congenital heart defects induced by aneuploidy of chromosome 21. |
format | Online Article Text |
id | pubmed-10578300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105783002023-10-16 Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects Alonzo, Matthew Ye, Shiqiao Beckman, Brian Texter, Karen Garg, Vidu Zhao, Ming-Tao Stem Cell Res Article Down syndrome is a congenital disorder resulting from an extra full or partial chromosome 21, which is characterized by a spectrum of systemic developmental abnormalities, including those affecting the cardiovascular system. Here, we generated an iPSC line from peripheral blood mononuclear cells of a male adolescent with Down syndrome-associated congenital heart defects through Sendai virus-mediated transfection of 4 Yamanaka factors. This line exhibited normal morphology, expressed pluripotency markers, trisomy 21 karyotype, and could be differentiated into three germ layers. This iPSC line can be used for studying cellular and developmental etiologies of congenital heart defects induced by aneuploidy of chromosome 21. 2023-09 2023-06-24 /pmc/articles/PMC10578300/ /pubmed/37393719 http://dx.doi.org/10.1016/j.scr.2023.103156 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Alonzo, Matthew Ye, Shiqiao Beckman, Brian Texter, Karen Garg, Vidu Zhao, Ming-Tao Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title | Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title_full | Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title_fullStr | Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title_full_unstemmed | Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title_short | Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects |
title_sort | creation of ipsc line nchi004-a from a patient with down syndrome and congenital heart defects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578300/ https://www.ncbi.nlm.nih.gov/pubmed/37393719 http://dx.doi.org/10.1016/j.scr.2023.103156 |
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