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Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA
Jaw periosteal cells (JPCs) represent a suitable stem cell source for bone tissue engineering (BTE) applications. However, challenges associated with limited cell numbers, stressful cell sorting, or the occurrence of cell senescence during in vitro passaging and the associated insufficient osteogeni...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480539/ https://www.ncbi.nlm.nih.gov/pubmed/30987077 http://dx.doi.org/10.3390/ijms20071648 |
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author | Umrath, Felix Steinle, Heidrun Weber, Marbod Wendel, Hans-Peter Reinert, Siegmar Alexander, Dorothea Avci-Adali, Meltem |
author_facet | Umrath, Felix Steinle, Heidrun Weber, Marbod Wendel, Hans-Peter Reinert, Siegmar Alexander, Dorothea Avci-Adali, Meltem |
author_sort | Umrath, Felix |
collection | PubMed |
description | Jaw periosteal cells (JPCs) represent a suitable stem cell source for bone tissue engineering (BTE) applications. However, challenges associated with limited cell numbers, stressful cell sorting, or the occurrence of cell senescence during in vitro passaging and the associated insufficient osteogenic potential in vitro of JPCs and other mesenchymal stem/stromal cells (MSCs) are main hurdles and still need to be solved. In this study, for the first time, induced pluripotent stem cells (iPSCs) were generated from human JPCs to open up a new source of stem cells for BTE. For this purpose, a non-integrating self-replicating RNA (srRNA) encoding reprogramming factors and green fluorescent protein (GFP) as a reporter was used to obtain JPC-iPSCs with a feeder- and xeno-free reprogramming protocol to meet the highest safety standards for future clinical applications. Furthermore, to analyze the potential of these iPSCs as a source of osteogenic progenitor cells, JPC-iPSCs were differentiated into iPSC-derived mesenchymal stem/stromal like cells (iMSCs) and further differentiated to the osteogenic lineage under xeno-free conditions. The produced iMSCs displayed MSC marker expression and morphology as well as strong mineralization during osteogenic differentiation. |
format | Online Article Text |
id | pubmed-6480539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64805392019-04-29 Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA Umrath, Felix Steinle, Heidrun Weber, Marbod Wendel, Hans-Peter Reinert, Siegmar Alexander, Dorothea Avci-Adali, Meltem Int J Mol Sci Article Jaw periosteal cells (JPCs) represent a suitable stem cell source for bone tissue engineering (BTE) applications. However, challenges associated with limited cell numbers, stressful cell sorting, or the occurrence of cell senescence during in vitro passaging and the associated insufficient osteogenic potential in vitro of JPCs and other mesenchymal stem/stromal cells (MSCs) are main hurdles and still need to be solved. In this study, for the first time, induced pluripotent stem cells (iPSCs) were generated from human JPCs to open up a new source of stem cells for BTE. For this purpose, a non-integrating self-replicating RNA (srRNA) encoding reprogramming factors and green fluorescent protein (GFP) as a reporter was used to obtain JPC-iPSCs with a feeder- and xeno-free reprogramming protocol to meet the highest safety standards for future clinical applications. Furthermore, to analyze the potential of these iPSCs as a source of osteogenic progenitor cells, JPC-iPSCs were differentiated into iPSC-derived mesenchymal stem/stromal like cells (iMSCs) and further differentiated to the osteogenic lineage under xeno-free conditions. The produced iMSCs displayed MSC marker expression and morphology as well as strong mineralization during osteogenic differentiation. MDPI 2019-04-03 /pmc/articles/PMC6480539/ /pubmed/30987077 http://dx.doi.org/10.3390/ijms20071648 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Umrath, Felix Steinle, Heidrun Weber, Marbod Wendel, Hans-Peter Reinert, Siegmar Alexander, Dorothea Avci-Adali, Meltem Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title | Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title_full | Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title_fullStr | Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title_full_unstemmed | Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title_short | Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA |
title_sort | generation of ipscs from jaw periosteal cells using self-replicating rna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480539/ https://www.ncbi.nlm.nih.gov/pubmed/30987077 http://dx.doi.org/10.3390/ijms20071648 |
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