A comparative study on different stemness gene expression between dental pulp stem cells vs. dental bud stem cells.
Cell Differentiation
/ genetics
Child
DNA-Binding Proteins
/ genetics
Dental Pulp
/ cytology
Gene Expression Profiling
Humans
Kruppel-Like Factor 4
Kruppel-Like Transcription Factors
/ genetics
Male
Nanog Homeobox Protein
/ genetics
Octamer Transcription Factor-3
/ genetics
SOXB1 Transcription Factors
/ genetics
Stem Cells
/ cytology
Transcription Factors
/ genetics
Journal
European review for medical and pharmacological sciences
ISSN: 2284-0729
Titre abrégé: Eur Rev Med Pharmacol Sci
Pays: Italy
ID NLM: 9717360
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
entrez:
7
3
2019
pubmed:
7
3
2019
medline:
28
7
2020
Statut:
ppublish
Résumé
The clinical use of mesenchymal stem cells (MSCs) in regenerative medicine either in tissue repair or tissue reconstruction has given highly interesting results thanks to their particular nature. Sources that have attracted the attention of medical scientists from where stem cells (SCs) in adults could be obtained are different and, dental tissues have certainly become an optimal source of MSCs. Dental tissue is a main reservoir of two types of MSCs dental bud (DBSCs) that constitute the immature precursor of the tooth and dental pulp (DPSCs) that are derived from dental inner pulp and partly from dental follicle tissue and can differentiate into several cell phenotypes as osteoblast, chondrocyte, hepatocytes, cardiomyocytes, neuron and β cells. Normal impacted third molars and tooth buds were collected from adults and adolescents underwent to extractions for orthodontic reasons. The expression of the five stemness genes Nanog, OCT4, Sox2, c-Myc and Klf4 were investigated by qRT-PCR in two different dental stem/progenitor cells: dental pulp stem cells (DPSCs) and stem cells from dental bud (DBSCs), differentiated toward osteoblastic phenotype and not. Both DPSCs and DBSCs are easy to access and we found their expression of the typical mesenchymal stemness makers and osteogenic capacity due to the effective presence of embryonic gene regulators like Nanog, OCT4, Sox2, c-Myc and Klf4. Both DBSCs and DPSCs could represent a valid tool in regenerative medicine and translational applications. The results depicted here provide, for the first time to our knowledge, a comparative outcome about the stemness properties generated from accessible tissues such as DPSCs and DBSCs. These two types of SCs showed few different distinctive genetic traits supposedly in relation to their origin, location and stage of maturation. Certainly these SCs reserve solid potential for human clinical application in autologous procedure for bone, hard tissue and soft tissue regeneration, easy to isolate, ready availability, high-biocompatibility and safety and no ethical restrictions.
Identifiants
pubmed: 30840286
doi: 10.26355/eurrev_201902_17122
pii:
doi:
Substances chimiques
DNA-Binding Proteins
0
KLF4 protein, human
0
Kruppel-Like Factor 4
0
Kruppel-Like Transcription Factors
0
MYCBP protein, human
0
NANOG protein, human
0
Nanog Homeobox Protein
0
Octamer Transcription Factor-3
0
POU5F1 protein, human
0
SOX2 protein, human
0
SOXB1 Transcription Factors
0
Transcription Factors
0
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM