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Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth
BACKGROUND: Dental pulp stem cells (DPSCs) play an important role in tissue regeneration. This study compares the growth kinetics and characterization of third molar and first premolar human DPSCs. MATERIAL AND METHODS: Dental pulp tissues were isolated from human first premolar and third molar teet...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303312/ https://www.ncbi.nlm.nih.gov/pubmed/28210430 http://dx.doi.org/10.4317/jced.52824 |
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author | Mehrabani, Davood Mahdiyar, Parisa Torabi, Kianoosh Robati, Reza Zare, Shahrokh Dianatpour, Mehdi Tamadon, Amin |
author_facet | Mehrabani, Davood Mahdiyar, Parisa Torabi, Kianoosh Robati, Reza Zare, Shahrokh Dianatpour, Mehdi Tamadon, Amin |
author_sort | Mehrabani, Davood |
collection | PubMed |
description | BACKGROUND: Dental pulp stem cells (DPSCs) play an important role in tissue regeneration. This study compares the growth kinetics and characterization of third molar and first premolar human DPSCs. MATERIAL AND METHODS: Dental pulp tissues were isolated from human first premolar and third molar teeth and were digested by treating them with collagenase type I. Single-cell suspensions from each dental pulp were seeded in T25 culture flasks and the media were replaced every 3 days until 70% confluence. The cells were enumerated to determine the population doubling time (PDT). Cells were characterized using flow cytometry, RT-PCR and osteogenic medium for differentiation of DPSCs. Karyotyping assay was also performed till passage 7th. RESULTS: The DPSCs had spindle-shaped morphology. There was an increase in PDT in third molar DPSCs when compared to first premolar teeth. Positive expression of CD44, CD73, and CD90 and negative expression of CD34 and CD45 were illustrated. A normal karyotype was visible for all seven passages. The Alizarin red staining was positive for osteogenic induction of DPSCs. CONCLUSIONS: When DPSCs are needed, third molar teeth can be a good and convenient candidate for cell transplantation, yielding high number of cells with mesenchymal characteristics. They can be a source for further investigations in vitro and work on tissue engineering protocols. Key words:Stem cells, dental pulp, growth kinetics, characterization. |
format | Online Article Text |
id | pubmed-5303312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53033122017-02-16 Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth Mehrabani, Davood Mahdiyar, Parisa Torabi, Kianoosh Robati, Reza Zare, Shahrokh Dianatpour, Mehdi Tamadon, Amin J Clin Exp Dent Research BACKGROUND: Dental pulp stem cells (DPSCs) play an important role in tissue regeneration. This study compares the growth kinetics and characterization of third molar and first premolar human DPSCs. MATERIAL AND METHODS: Dental pulp tissues were isolated from human first premolar and third molar teeth and were digested by treating them with collagenase type I. Single-cell suspensions from each dental pulp were seeded in T25 culture flasks and the media were replaced every 3 days until 70% confluence. The cells were enumerated to determine the population doubling time (PDT). Cells were characterized using flow cytometry, RT-PCR and osteogenic medium for differentiation of DPSCs. Karyotyping assay was also performed till passage 7th. RESULTS: The DPSCs had spindle-shaped morphology. There was an increase in PDT in third molar DPSCs when compared to first premolar teeth. Positive expression of CD44, CD73, and CD90 and negative expression of CD34 and CD45 were illustrated. A normal karyotype was visible for all seven passages. The Alizarin red staining was positive for osteogenic induction of DPSCs. CONCLUSIONS: When DPSCs are needed, third molar teeth can be a good and convenient candidate for cell transplantation, yielding high number of cells with mesenchymal characteristics. They can be a source for further investigations in vitro and work on tissue engineering protocols. Key words:Stem cells, dental pulp, growth kinetics, characterization. Medicina Oral S.L. 2017-02-01 /pmc/articles/PMC5303312/ /pubmed/28210430 http://dx.doi.org/10.4317/jced.52824 Text en Copyright: © 2017 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Mehrabani, Davood Mahdiyar, Parisa Torabi, Kianoosh Robati, Reza Zare, Shahrokh Dianatpour, Mehdi Tamadon, Amin Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title | Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title_full | Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title_fullStr | Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title_full_unstemmed | Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title_short | Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth |
title_sort | growth kinetics and characterization of human dental pulp stem cells: comparison between third molar and first premolar teeth |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303312/ https://www.ncbi.nlm.nih.gov/pubmed/28210430 http://dx.doi.org/10.4317/jced.52824 |
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