Cargando…
Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells
BACKGROUND: Stem cells are normally isolated from dental pulps using the enzymatic digestion or the outgrowth method. However, the effects of the isolation method on the quality of the isolated stem cells are not studied in detail in murine models. The aim of this study was to compare the matrices s...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473353/ https://www.ncbi.nlm.nih.gov/pubmed/28626603 http://dx.doi.org/10.7717/peerj.3180 |
_version_ | 1783244279475339264 |
---|---|
author | Megat Abdul Wahab, Rohaya Mohamed Rozali, Nur Akmal Senafi, Sahidan Zainol Abidin, Intan Zarina Zainal Ariffin, Zaidah Zainal Ariffin, Shahrul Hisham |
author_facet | Megat Abdul Wahab, Rohaya Mohamed Rozali, Nur Akmal Senafi, Sahidan Zainol Abidin, Intan Zarina Zainal Ariffin, Zaidah Zainal Ariffin, Shahrul Hisham |
author_sort | Megat Abdul Wahab, Rohaya |
collection | PubMed |
description | BACKGROUND: Stem cells are normally isolated from dental pulps using the enzymatic digestion or the outgrowth method. However, the effects of the isolation method on the quality of the isolated stem cells are not studied in detail in murine models. The aim of this study was to compare the matrices secreted by osteoblast and chondrocytes differentiated from dental pulp stem cells isolated through different means. METHOD: DPSC from murine incisors were isolated through either the outgrowth (DPSC-OG) or the enzymatic digestion (DPSC-ED) method. Cells at passage 4 were used in this study. The cells were characterized through morphology and expression of cell surface markers. The cells’ doubling time when cultured using different seeding densities was calculated and analyzed using one-way ANOVA and Tukey’s multiple comparison post-test. The ability of cells to differentiate to chondrocyte and osteoblast was evaluated through staining and analysis on the matrices secreted. RESULTS: Gene expression analysis showed that DPSC-OG and DPSC-ED expressed dental pulp mesenchymal stem cell markers, but not hematopoietic stem cell markers. The least number of cells that could have been used to culture DPSC-OG and DPSC-ED with the shortest doubling time was 5 × 10(2) cells/cm(2) (11.49 ± 2.16 h) and 1 × 10(2) cells/cm(2) (10.55 h ± 0.50), respectively. Chondrocytes differentiated from DPSC-ED produced 2 times more proteoglycan and at a faster rate than DPSC-OG. FTIR revealed that DPSC-ED differentiated into osteoblast also secreted matrix, which more resembled a calvaria. DISCUSSION: Isolation approaches might have influenced the cell populations obtained. This, in turn, resulted in cells with different proliferation and differentiation capability. While both DPSC-OG and DPSC-ED expressed mesenchymal stem cell markers, the percentage of cells carrying each marker might have differed between the two methods. Regardless, enzymatic digestion clearly yielded cells with better characteristics than outgrowth. |
format | Online Article Text |
id | pubmed-5473353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54733532017-06-16 Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells Megat Abdul Wahab, Rohaya Mohamed Rozali, Nur Akmal Senafi, Sahidan Zainol Abidin, Intan Zarina Zainal Ariffin, Zaidah Zainal Ariffin, Shahrul Hisham PeerJ Biotechnology BACKGROUND: Stem cells are normally isolated from dental pulps using the enzymatic digestion or the outgrowth method. However, the effects of the isolation method on the quality of the isolated stem cells are not studied in detail in murine models. The aim of this study was to compare the matrices secreted by osteoblast and chondrocytes differentiated from dental pulp stem cells isolated through different means. METHOD: DPSC from murine incisors were isolated through either the outgrowth (DPSC-OG) or the enzymatic digestion (DPSC-ED) method. Cells at passage 4 were used in this study. The cells were characterized through morphology and expression of cell surface markers. The cells’ doubling time when cultured using different seeding densities was calculated and analyzed using one-way ANOVA and Tukey’s multiple comparison post-test. The ability of cells to differentiate to chondrocyte and osteoblast was evaluated through staining and analysis on the matrices secreted. RESULTS: Gene expression analysis showed that DPSC-OG and DPSC-ED expressed dental pulp mesenchymal stem cell markers, but not hematopoietic stem cell markers. The least number of cells that could have been used to culture DPSC-OG and DPSC-ED with the shortest doubling time was 5 × 10(2) cells/cm(2) (11.49 ± 2.16 h) and 1 × 10(2) cells/cm(2) (10.55 h ± 0.50), respectively. Chondrocytes differentiated from DPSC-ED produced 2 times more proteoglycan and at a faster rate than DPSC-OG. FTIR revealed that DPSC-ED differentiated into osteoblast also secreted matrix, which more resembled a calvaria. DISCUSSION: Isolation approaches might have influenced the cell populations obtained. This, in turn, resulted in cells with different proliferation and differentiation capability. While both DPSC-OG and DPSC-ED expressed mesenchymal stem cell markers, the percentage of cells carrying each marker might have differed between the two methods. Regardless, enzymatic digestion clearly yielded cells with better characteristics than outgrowth. PeerJ Inc. 2017-06-14 /pmc/articles/PMC5473353/ /pubmed/28626603 http://dx.doi.org/10.7717/peerj.3180 Text en ©2017 Megat Abdul Wahab et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Biotechnology Megat Abdul Wahab, Rohaya Mohamed Rozali, Nur Akmal Senafi, Sahidan Zainol Abidin, Intan Zarina Zainal Ariffin, Zaidah Zainal Ariffin, Shahrul Hisham Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title | Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title_full | Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title_fullStr | Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title_full_unstemmed | Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title_short | Impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
title_sort | impact of isolation method on doubling time and the quality of chondrocyte and osteoblast differentiated from murine dental pulp stem cells |
topic | Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473353/ https://www.ncbi.nlm.nih.gov/pubmed/28626603 http://dx.doi.org/10.7717/peerj.3180 |
work_keys_str_mv | AT megatabdulwahabrohaya impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells AT mohamedrozalinurakmal impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells AT senafisahidan impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells AT zainolabidinintanzarina impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells AT zainalariffinzaidah impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells AT zainalariffinshahrulhisham impactofisolationmethodondoublingtimeandthequalityofchondrocyteandosteoblastdifferentiatedfrommurinedentalpulpstemcells |