hPL promotes osteogenic differentiation of stem cells in 3D scaffolds

Human platelet lysate (hPL) has been considered as the preferred supplement for the xeno-free stem cell culture for many years. However, the biological effect of hPL on the proliferation and differentiation of dental stem cells combined with the use of medical grade synthetic biomaterial is still un...

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Published inPloS one Vol. 14; no. 5; p. e0215667
Main Authors Jafar, Hanan, Abuarqoub, Duaa, Ababneh, Nidaa, Hasan, Maram, Al-Sotari, Shrouq, Aslam, Nazneen, Kailani, Mohammed, Ammoush, Mohammed, Shraideh, Ziad, Awidi, Abdalla
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 07.05.2019
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Abstract Human platelet lysate (hPL) has been considered as the preferred supplement for the xeno-free stem cell culture for many years. However, the biological effect of hPL on the proliferation and differentiation of dental stem cells combined with the use of medical grade synthetic biomaterial is still under investigation. Thus, the optimal scaffold composition, cell type and specific growth conditions, yet need to be formulated. In this study, we aimed to investigate the regenerative potential of dental stem cells seeded on synthetic scaffolds and maintained in osteogenic media supplemented with either hPL or xeno-derived fetal bovine serum (FBS). Two types of dental stem cells were isolated from human impacted third molars and intact teeth; stem cells of apical papilla (SCAP) and periodontal ligament stem cells (PDLSCs). Cells were expanded in cell culture media supplemented with either hPL or FBS. Consequently, proliferative capacity, immunophenotypic characteristics and multilineage differentiation potential of the derived cells were evaluated on monolayer culture (2D) and on synthetic scaffolds fabricated from poly 'lactic-co-glycolic' acid (PLGA) (3D). The functionality of the induced cells was examined by measuring the concentration of osteogenic markers ALP, OCN and OPN at different time points. Our results indicate that the isolated dental stem cells showed similar mesenchymal characteristics when cultured on hPL or FBS-containing culture media. Scanning electron microscopy (SEM) and H&E staining revealed the proper adherence of the derived cells on the 3D scaffold cultures. Moreover, the increase in the concentration of osteogenic markers proved that hPL was able to produce functional osteoblasts in both culture conditions (2D and 3D), in a way similar to FBS culture. These results reveal that hPL provides a suitable substitute to the animal-derived serum, for the growth and functionality of both SCAP and PDLSCs. Thus the use of hPL, in combination with PLGA scaffolds, can be useful in future clinical trials for dental regeneration.
AbstractList Human platelet lysate (hPL) has been considered as the preferred supplement for the xeno-free stem cell culture for many years. However, the biological effect of hPL on the proliferation and differentiation of dental stem cells combined with the use of medical grade synthetic biomaterial is still under investigation. Thus, the optimal scaffold composition, cell type and specific growth conditions, yet need to be formulated. In this study, we aimed to investigate the regenerative potential of dental stem cells seeded on synthetic scaffolds and maintained in osteogenic media supplemented with either hPL or xeno-derived fetal bovine serum (FBS). Two types of dental stem cells were isolated from human impacted third molars and intact teeth; stem cells of apical papilla (SCAP) and periodontal ligament stem cells (PDLSCs). Cells were expanded in cell culture media supplemented with either hPL or FBS. Consequently, proliferative capacity, immunophenotypic characteristics and multilineage differentiation potential of the derived cells were evaluated on monolayer culture (2D) and on synthetic scaffolds fabricated from poly ’lactic-co-glycolic’ acid (PLGA) (3D). The functionality of the induced cells was examined by measuring the concentration of osteogenic markers ALP, OCN and OPN at different time points. Our results indicate that the isolated dental stem cells showed similar mesenchymal characteristics when cultured on hPL or FBS-containing culture media. Scanning electron microscopy (SEM) and H&E staining revealed the proper adherence of the derived cells on the 3D scaffold cultures. Moreover, the increase in the concentration of osteogenic markers proved that hPL was able to produce functional osteoblasts in both culture conditions (2D and 3D), in a way similar to FBS culture. These results reveal that hPL provides a suitable substitute to the animal-derived serum, for the growth and functionality of both SCAP and PDLSCs. Thus the use of hPL, in combination with PLGA scaffolds, can be useful in future clinical trials for dental regeneration.
Audience Academic
Author Ababneh, Nidaa
Ammoush, Mohammed
Jafar, Hanan
Awidi, Abdalla
Abuarqoub, Duaa
Aslam, Nazneen
Al-Sotari, Shrouq
Shraideh, Ziad
Hasan, Maram
Kailani, Mohammed
AuthorAffiliation Northeastern University, UNITED STATES
3 Department of Chemistry, School of Sciences, The University of Jordan, Amman, Jordan
5 Department of Biological Sciences, School of Sciences, The University of Jordan, Amman, Jordan
1 Cell Therapy Center, The University of Jordan, Amman, Jordan
2 School of Medicine, The University of Jordan, Amman, Jordan
4 Dental Department, King Hussein Medical Center (KHMC), Royal Medical Service, Amman, Jordan
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ContentType Journal Article
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2019 Jafar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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– notice: 2019 Jafar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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SSID ssj0053866
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Snippet Human platelet lysate (hPL) has been considered as the preferred supplement for the xeno-free stem cell culture for many years. However, the biological effect...
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StartPage e0215667
SubjectTerms Biocompatibility
Biological effects
Biological products
Biology and Life Sciences
Biomarkers
Biomaterials
Biomedical materials
Biotechnology
Blood platelets
Blood Platelets - metabolism
Cell culture
Cell Differentiation - drug effects
Cell proliferation
Cell Proliferation - drug effects
Clinical trials
Culture media
Differentiation (biology)
Electron microscopy
Fetal calf serum
Gene expression
Growth conditions
Health aspects
Humans
Ligaments
Medical research
Medicine
Medicine and Health Sciences
Mesenchymal stem cells
Mesenchyme
Methods
Microscopy
Molars
Odontogenesis - drug effects
Osteoblasts
Osteogenesis
Osteogenesis - drug effects
Patient outcomes
Periodontal ligament
Physical Sciences
Polylactic acid
Polylactic Acid-Polyglycolic Acid Copolymer - chemistry
Polylactide-co-glycolide
Regeneration
Research and Analysis Methods
Scaffolds
Scanning electron microscopy
Scanning transmission electron microscopy
Stem cell transplantation
Stem cells
Stem Cells - cytology
Stem Cells - drug effects
Teeth
Tissue engineering
Tissue Scaffolds
Transplants & implants
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Title hPL promotes osteogenic differentiation of stem cells in 3D scaffolds
URI https://www.ncbi.nlm.nih.gov/pubmed/31063489
https://www.proquest.com/docview/2221212425
https://search.proquest.com/docview/2231889367
https://pubmed.ncbi.nlm.nih.gov/PMC6504042
https://doaj.org/article/02d93f36ffd5416e9d9b53a4aa52df4f
http://dx.doi.org/10.1371/journal.pone.0215667
Volume 14
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