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Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters
Human dental tissues are sources of neural crest origin multipotent stem cells whose regenerative potential is a focus of extensive studies. Rational programming of clinical applications requires a more detailed knowledge of the characters inherited from neural crest. Investigation of neural crest c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268458/ https://www.ncbi.nlm.nih.gov/pubmed/28125654 http://dx.doi.org/10.1371/journal.pone.0170321 |
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author | Gazarian, Karlen G. Ramírez-García, Luis R. |
author_facet | Gazarian, Karlen G. Ramírez-García, Luis R. |
author_sort | Gazarian, Karlen G. |
collection | PubMed |
description | Human dental tissues are sources of neural crest origin multipotent stem cells whose regenerative potential is a focus of extensive studies. Rational programming of clinical applications requires a more detailed knowledge of the characters inherited from neural crest. Investigation of neural crest cells generated from human pluripotent stem cells provided opportunity for their comparison with the postnatal dental cells. The purpose of this study was to investigate the role of the culture conditions in the expression by dental cells of neural crest characters. The results of the study demonstrate that specific neural crest cells requirements, serum-free, active WNT signaling and inactive SMAD 2/3, are needed for the activity of the neural crest characters in dental cells. Specifically, the decreasing concentration of fetal bovine serum (FBS) from regularly used for dental cells 10% to 2% and below, or using serum-free medium, led to emergence of a subset of epithelial-like cells expressing the two key neural crest markers, p75 and HNK-1. Further, the serum-free medium supplemented with neural crest signaling requirements (WNT inducer BIO and TGF-β inhibitor REPSOX), induced epithelial-like phenotype, upregulated the p75, Sox10 and E-Cadherin and downregulated the mesenchymal genes (SNAIL1, ZEB1, TWIST). An expansion medium containing 2% FBS allowed to obtain an epithelial/mesenchymal SHED population showing high proliferation, clonogenic, multi-lineage differentiation capacities. Future experiments will be required to determine the effects of these features on regenerative potential of this novel SHED population. |
format | Online Article Text |
id | pubmed-5268458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52684582017-02-06 Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters Gazarian, Karlen G. Ramírez-García, Luis R. PLoS One Research Article Human dental tissues are sources of neural crest origin multipotent stem cells whose regenerative potential is a focus of extensive studies. Rational programming of clinical applications requires a more detailed knowledge of the characters inherited from neural crest. Investigation of neural crest cells generated from human pluripotent stem cells provided opportunity for their comparison with the postnatal dental cells. The purpose of this study was to investigate the role of the culture conditions in the expression by dental cells of neural crest characters. The results of the study demonstrate that specific neural crest cells requirements, serum-free, active WNT signaling and inactive SMAD 2/3, are needed for the activity of the neural crest characters in dental cells. Specifically, the decreasing concentration of fetal bovine serum (FBS) from regularly used for dental cells 10% to 2% and below, or using serum-free medium, led to emergence of a subset of epithelial-like cells expressing the two key neural crest markers, p75 and HNK-1. Further, the serum-free medium supplemented with neural crest signaling requirements (WNT inducer BIO and TGF-β inhibitor REPSOX), induced epithelial-like phenotype, upregulated the p75, Sox10 and E-Cadherin and downregulated the mesenchymal genes (SNAIL1, ZEB1, TWIST). An expansion medium containing 2% FBS allowed to obtain an epithelial/mesenchymal SHED population showing high proliferation, clonogenic, multi-lineage differentiation capacities. Future experiments will be required to determine the effects of these features on regenerative potential of this novel SHED population. Public Library of Science 2017-01-26 /pmc/articles/PMC5268458/ /pubmed/28125654 http://dx.doi.org/10.1371/journal.pone.0170321 Text en © 2017 Gazarian, Ramírez-García http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gazarian, Karlen G. Ramírez-García, Luis R. Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title | Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title_full | Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title_fullStr | Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title_full_unstemmed | Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title_short | Human Deciduous Teeth Stem Cells (SHED) Display Neural Crest Signature Characters |
title_sort | human deciduous teeth stem cells (shed) display neural crest signature characters |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268458/ https://www.ncbi.nlm.nih.gov/pubmed/28125654 http://dx.doi.org/10.1371/journal.pone.0170321 |
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