The Differentiation Potential of Human Natal Dental Pulp Stem Cells into Insulin-Producing Cells
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
29256855
DOI
10.14712/fb2017063040132
PII: file/5848/fb2017a0019.pdf
Knihovny.cz E-resources
- MeSH
- Insulin-Secreting Cells cytology metabolism MeSH
- Cell Differentiation physiology MeSH
- C-Peptide metabolism MeSH
- Diabetes Mellitus, Type 1 metabolism MeSH
- Homeodomain Proteins metabolism MeSH
- Immunohistochemistry MeSH
- Insulin metabolism MeSH
- Stem Cells cytology metabolism MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Mesenchymal Stem Cells cytology metabolism MeSH
- Flow Cytometry MeSH
- Trans-Activators metabolism MeSH
- Transcription Factor HES-1 metabolism MeSH
- Dental Pulp cytology MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- C-Peptide MeSH
- HES1 protein, human MeSH Browser
- Homeodomain Proteins MeSH
- Insulin MeSH
- pancreatic and duodenal homeobox 1 protein MeSH Browser
- Trans-Activators MeSH
- Transcription Factor HES-1 MeSH
Mesenchymal stem cells have the ability to differentiate into insulin-producing cells, raising the hope for diabetes mellitus treatment. The aim of this research was to study the ability of stem cells from discarded natal teeth to differentiate into insulinproducing cells. Two vital human natal teeth were obtained from a healthy 2-day-old female. Stem cells from the dental pulp were isolated, cultured under xenogenic-free conditions, propagated and characterized. Proliferative activity, population doubling time and viability were measured, and the multipotent differentiation ability was investigated. A twostep protocol was used to induce the human natal dental pulp stem cells to differentiate into insulinproducing cells. Phenotypic analysis was done using flow cytometry. Immunohistochemistry was performed to detect insulin and C-peptide. PDX1, HES1 and Glut2 gene expression analysis was performed by quantitative reverse transcription-polymerase chain reaction. Human natal dental pulp stem cells were able to undergo osteogenic, chondrogenic and adipogenic differentiation upon exposure to the specific differentiation media for each lineage. Their differentiation into insulin-producing cells was confirmed by expression of C-peptide and insulin, as well as by 975.4 % higher expression of PDX-1 and 469.5 % higher expression of HES1 in comparison to the cells cultivated in standard cultivation media. Glut2 transporter mRNA was absent in the non-differentiated cells, and differentiation of the stem cells into insulin-producing cells induced appearance of the mRNA of this transporter. We were the first to demonstrate that stem cells obtained from the pulp of natal teeth could be differentiated into insulinproducing cells, which might prove useful in the stem cell therapy for type 1 diabetes.
References provided by Crossref.org
Intra-Individual Variability of Human Dental Pulp Stem Cell Features Isolated from the Same Donor
The Effects of Cryogenic Storage on Human Dental Pulp Stem Cells