Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp

Human dental pulp stem cells are adult multipotent stem cells isolated from dental pulp tissue. Our objective was to determine in vitro culture technique for stem cells from deciduous tooth (SHED) and permanent tooth (DPSC) through cell passage identification, the effect of trypsin-EDTA and prolifer...

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Published in:Sains Malaysiana
Main Author: Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
Format: Article
Language:English
Published: Penerbit Universiti Kebangsaan Malaysia 2019
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075444819&doi=10.17576%2fjsm-2019-4809-06&partnerID=40&md5=212b7412555c6036e0042e015e9b61b2
id 2-s2.0-85075444819
spelling 2-s2.0-85075444819
Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
2019
Sains Malaysiana
48
9
10.17576/jsm-2019-4809-06
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075444819&doi=10.17576%2fjsm-2019-4809-06&partnerID=40&md5=212b7412555c6036e0042e015e9b61b2
Human dental pulp stem cells are adult multipotent stem cells isolated from dental pulp tissue. Our objective was to determine in vitro culture technique for stem cells from deciduous tooth (SHED) and permanent tooth (DPSC) through cell passage identification, the effect of trypsin-EDTA and proliferation potential, and to characterize both cells using molecular markers profile. Enzyme digestion method was used on dental pulp tissue from deciduous and permanent tooth for SHED and DPSC isolation, respectively. Both cells were cultured at passage 1 until 5 and trypan blue assay was used to obtain growth curve in determining cell population doubling time (PDT) for each passage. Effect of trypsin-EDTA on both cells were studied using Alamar blue assay to determine optimum incubation time for subculturing process. Cell proliferation potential for both cells within 21 days was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Cell characterization through molecular biology markers was performed using RT-PCR. Both cells at all passages appeared fibroblast-like. SHED and DPSC at passage 3 exhibited the lowest PDT with 43 ± 2.3 and 63 ± 3.1 h, respectively. SHED exposed to trypsin-EDTA showed decrease in cell viability percentage compared to DPSC. Cell growth for SHED was ∼2.3-fold higher than DPSC. Both cells expressed mesenchymal stem cell markers and not hematopoietic stem cell markers. In conclusion, homogenous morphology and lowest PDT value indicated that cells at passage 3 are the best to determine proliferation potential and molecular markers expression. SHED proliferated better than DPSC. However, DPSC was more resistant to trypsin-EDTA than SHED. Based on molecular marker profile, both cells are mesenchymal stem cells. © 2019 Penerbit Universiti Kebangsaan Malaysia. All rights reserved.
Penerbit Universiti Kebangsaan Malaysia
1266039
English
Article
All Open Access; Gold Open Access
author Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
spellingShingle Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
author_facet Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
author_sort Ariffin S.H.Z.; Manogaran T.; Abidin I.Z.Z.; Ariffin Z.Z.; Pengajian Biologi P.; Wahab R.M.A.
title Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
title_short Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
title_full Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
title_fullStr Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
title_full_unstemmed Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
title_sort Culture and molecular markers characterization of Stem Cells from Human Deciduous (SHED) and Permanent (DPSC) teeth pulp
publishDate 2019
container_title Sains Malaysiana
container_volume 48
container_issue 9
doi_str_mv 10.17576/jsm-2019-4809-06
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075444819&doi=10.17576%2fjsm-2019-4809-06&partnerID=40&md5=212b7412555c6036e0042e015e9b61b2
description Human dental pulp stem cells are adult multipotent stem cells isolated from dental pulp tissue. Our objective was to determine in vitro culture technique for stem cells from deciduous tooth (SHED) and permanent tooth (DPSC) through cell passage identification, the effect of trypsin-EDTA and proliferation potential, and to characterize both cells using molecular markers profile. Enzyme digestion method was used on dental pulp tissue from deciduous and permanent tooth for SHED and DPSC isolation, respectively. Both cells were cultured at passage 1 until 5 and trypan blue assay was used to obtain growth curve in determining cell population doubling time (PDT) for each passage. Effect of trypsin-EDTA on both cells were studied using Alamar blue assay to determine optimum incubation time for subculturing process. Cell proliferation potential for both cells within 21 days was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Cell characterization through molecular biology markers was performed using RT-PCR. Both cells at all passages appeared fibroblast-like. SHED and DPSC at passage 3 exhibited the lowest PDT with 43 ± 2.3 and 63 ± 3.1 h, respectively. SHED exposed to trypsin-EDTA showed decrease in cell viability percentage compared to DPSC. Cell growth for SHED was ∼2.3-fold higher than DPSC. Both cells expressed mesenchymal stem cell markers and not hematopoietic stem cell markers. In conclusion, homogenous morphology and lowest PDT value indicated that cells at passage 3 are the best to determine proliferation potential and molecular markers expression. SHED proliferated better than DPSC. However, DPSC was more resistant to trypsin-EDTA than SHED. Based on molecular marker profile, both cells are mesenchymal stem cells. © 2019 Penerbit Universiti Kebangsaan Malaysia. All rights reserved.
publisher Penerbit Universiti Kebangsaan Malaysia
issn 1266039
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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