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Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues
Human perinatal tissue is an abundant source of mesenchymal stromal cells(MSCs) and lacks the ethical concerns. Perinatal MSCs can be obtained from various tissues as like amnion, chorion, and umbilical cord. Still, little is known of the distinct nature of each MSC type. In this study, we successfu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820697/ https://www.ncbi.nlm.nih.gov/pubmed/27045658 http://dx.doi.org/10.1038/srep23544 |
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author | Kwon, Ahlm Kim, Yonggoo Kim, Myungshin Kim, Jiyeon Choi, Hayoung Jekarl, Dong Wook Lee, Seungok Kim, Jung Min Shin, Jong-Chul Park, In Yang |
author_facet | Kwon, Ahlm Kim, Yonggoo Kim, Myungshin Kim, Jiyeon Choi, Hayoung Jekarl, Dong Wook Lee, Seungok Kim, Jung Min Shin, Jong-Chul Park, In Yang |
author_sort | Kwon, Ahlm |
collection | PubMed |
description | Human perinatal tissue is an abundant source of mesenchymal stromal cells(MSCs) and lacks the ethical concerns. Perinatal MSCs can be obtained from various tissues as like amnion, chorion, and umbilical cord. Still, little is known of the distinct nature of each MSC type. In this study, we successfully isolated and cultured MSCs from amnion(AMSCs), chorion(CMSCs), and umbilical cord(UC-MSCs). Proliferation potential was different among them, that AMSCs revealed the lowest proliferation rate due to increased Annexin V and senescence-associated β-galactosidase positive cells. We demonstrated distinct characteristic gene expression according to the source of the original tissue using microarray. In particular, genes associated with apoptosis and senescence including CDKN2A were up-regulated in AMSCs. In CMSCs, genes associated with heart morphogenesis and blood circulation including HTR2B were up-regulated. Genes associated with neurological system processes including NPY were up-regulated in UC-MSCs. Quantitative RT-PCR confirmed the gene expression data. And in vitro differentiation of MSCs demonstrated that CMSCs and UC-MSCs had a more pronounced ability to differentiate into cardiomyocyte and neural cells, respectively. This study firstly demonstrated the innate tissue-specific differentiation potency of perinatal MSCs which can be helpful in choosing more adequate cell sources for better outcome in a specific disease. |
format | Online Article Text |
id | pubmed-4820697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48206972016-04-06 Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues Kwon, Ahlm Kim, Yonggoo Kim, Myungshin Kim, Jiyeon Choi, Hayoung Jekarl, Dong Wook Lee, Seungok Kim, Jung Min Shin, Jong-Chul Park, In Yang Sci Rep Article Human perinatal tissue is an abundant source of mesenchymal stromal cells(MSCs) and lacks the ethical concerns. Perinatal MSCs can be obtained from various tissues as like amnion, chorion, and umbilical cord. Still, little is known of the distinct nature of each MSC type. In this study, we successfully isolated and cultured MSCs from amnion(AMSCs), chorion(CMSCs), and umbilical cord(UC-MSCs). Proliferation potential was different among them, that AMSCs revealed the lowest proliferation rate due to increased Annexin V and senescence-associated β-galactosidase positive cells. We demonstrated distinct characteristic gene expression according to the source of the original tissue using microarray. In particular, genes associated with apoptosis and senescence including CDKN2A were up-regulated in AMSCs. In CMSCs, genes associated with heart morphogenesis and blood circulation including HTR2B were up-regulated. Genes associated with neurological system processes including NPY were up-regulated in UC-MSCs. Quantitative RT-PCR confirmed the gene expression data. And in vitro differentiation of MSCs demonstrated that CMSCs and UC-MSCs had a more pronounced ability to differentiate into cardiomyocyte and neural cells, respectively. This study firstly demonstrated the innate tissue-specific differentiation potency of perinatal MSCs which can be helpful in choosing more adequate cell sources for better outcome in a specific disease. Nature Publishing Group 2016-04-05 /pmc/articles/PMC4820697/ /pubmed/27045658 http://dx.doi.org/10.1038/srep23544 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kwon, Ahlm Kim, Yonggoo Kim, Myungshin Kim, Jiyeon Choi, Hayoung Jekarl, Dong Wook Lee, Seungok Kim, Jung Min Shin, Jong-Chul Park, In Yang Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title | Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title_full | Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title_fullStr | Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title_full_unstemmed | Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title_short | Tissue-specific Differentiation Potency of Mesenchymal Stromal Cells from Perinatal Tissues |
title_sort | tissue-specific differentiation potency of mesenchymal stromal cells from perinatal tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820697/ https://www.ncbi.nlm.nih.gov/pubmed/27045658 http://dx.doi.org/10.1038/srep23544 |
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