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 in | PloS one Vol. 14; no. 5; p. e0215667 |
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Main Authors | , , , , , , , , , |
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Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: Northeastern University, UNITED STATES – name: 4 Dental Department, King Hussein Medical Center (KHMC), Royal Medical Service, Amman, Jordan – name: 5 Department of Biological Sciences, School of Sciences, The University of Jordan, Amman, Jordan – name: 2 School of Medicine, The University of Jordan, Amman, Jordan – name: 1 Cell Therapy Center, The University of Jordan, Amman, Jordan – name: 3 Department of Chemistry, School of Sciences, The University of Jordan, Amman, Jordan |
Author_xml | – sequence: 1 givenname: Hanan orcidid: 0000-0001-6088-8783 surname: Jafar fullname: Jafar, Hanan organization: School of Medicine, The University of Jordan, Amman, Jordan – sequence: 2 givenname: Duaa surname: Abuarqoub fullname: Abuarqoub, Duaa organization: Cell Therapy Center, The University of Jordan, Amman, Jordan – sequence: 3 givenname: Nidaa surname: Ababneh fullname: Ababneh, Nidaa organization: Cell Therapy Center, The University of Jordan, Amman, Jordan – sequence: 4 givenname: Maram surname: Hasan fullname: Hasan, Maram organization: Cell Therapy Center, The University of Jordan, Amman, Jordan – sequence: 5 givenname: Shrouq surname: Al-Sotari fullname: Al-Sotari, Shrouq organization: Cell Therapy Center, The University of Jordan, Amman, Jordan – sequence: 6 givenname: Nazneen surname: Aslam fullname: Aslam, Nazneen organization: Cell Therapy Center, The University of Jordan, Amman, Jordan – sequence: 7 givenname: Mohammed surname: Kailani fullname: Kailani, Mohammed organization: Department of Chemistry, School of Sciences, The University of Jordan, Amman, Jordan – sequence: 8 givenname: Mohammed surname: Ammoush fullname: Ammoush, Mohammed organization: Dental Department, King Hussein Medical Center (KHMC), Royal Medical Service, Amman, Jordan – sequence: 9 givenname: Ziad surname: Shraideh fullname: Shraideh, Ziad organization: Department of Biological Sciences, School of Sciences, The University of Jordan, Amman, Jordan – sequence: 10 givenname: Abdalla surname: Awidi fullname: Awidi, Abdalla organization: School of Medicine, The University of Jordan, Amman, Jordan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31063489$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2019 Public Library of Science 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. 2019 Jafar et al 2019 Jafar et al |
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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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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 |
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