Generation of iPSCs from Jaw Periosteal Cells Using Self-Replicating RNA.
bone-tissue engineering
iPSC-derived mesenchymal stem/stromal like cells (iMSCs)
induced pluripotent stem cells (iPSCs)
jaw periosteal cells (JPCs)
reprogramming
self-replicating RNA
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
03 Apr 2019
03 Apr 2019
Historique:
received:
08
03
2019
revised:
30
03
2019
accepted:
30
03
2019
entrez:
17
4
2019
pubmed:
17
4
2019
medline:
31
7
2019
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 30987077
pii: ijms20071648
doi: 10.3390/ijms20071648
pmc: PMC6480539
pii:
doi:
Substances chimiques
Biomarkers
0
RNA
63231-63-0
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : AL 1486/6-1/AV 133/7-1
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