Differential Effects of Extracellular Matrix Glycoproteins Fibronectin and Laminin-5 on Dental Pulp Stem Cell Phenotypes and Responsiveness
-
Published:2023-02-08
Issue:2
Volume:14
Page:91
-
ISSN:2079-4983
-
Container-title:Journal of Functional Biomaterials
-
language:en
-
Short-container-title:JFB
Author:
Lee Hyungbin1, Bae Allen2, Kim John2, Kingsley Karl3ORCID
Affiliation:
1. Department of Advanced Education in Orthodontics, School of Medicine, University of Nevada—Las Vegas, Las Vegas, NV 89106, USA 2. Department of Clinical Sciences, School of Dental Medicine, University of Nevada—Las Vegas, Las Vegas, NV 89106, USA 3. Department of Biomedical Sciences, School of Dental Medicine, University of Nevada—Las Vegas, Las Vegas, NV 89106, USA
Abstract
Dental pulp stem cells (DPSCs) are mesenchymal stem cells (MSCs) with the potential to differentiate in a limited number of other tissue types. Some evidence has suggested the modulation of DPSC growth may be mediated, in part, by exogenous extracellular matrix (ECM) glycoproteins, including fibronectin (FN) and laminin-5 (LN5). Although preliminary research suggests that some ECM glycoproteins may work as functional biomaterials to modulate DPSC growth responses, the primary goal of this project is to determine the specific effects of FN and LN5 on DPSC growth and viability. Using an existing DPSC repository, n = 16 DPSC isolates were cultured and 96-well growth assays were performed, which revealed FN, LN5 and the combination of these were sufficient to induce statistically significant changes in growth among five (n = 5) DPSC isolates. In addition, the administration of FN (either alone or in combination) was sufficient to induce the expression of alkaline phosphatase (ALP) and dentin sialophosphoprotein (DSPP), while LN5 induced the expression of ALP only, suggesting differential responsiveness among DPSCs. Moreover, these responses appeared to correlate with the expression of MSC biomarkers NANOG, Oct4 and Sox2. These results add to the growing body of evidence suggesting that functional biomaterials, such as ECM glycoproteins FN and LN5, are sufficient to induce phenotypic and differentiation-specific effects in a specific subset of DPSC isolates. More research will be needed to determine which biomarkers or additional factors are necessary and sufficient to induce the differentiation and development of DPSCs ex vivo and in vitro for biomedical applications.
Funder
Office of Research at the University of Nevada, Las Vegas
Subject
Biomedical Engineering,Biomaterials
Reference70 articles.
1. Biological characteristics of dental pulp stem cells and their potential use in regenerative medicine;Honda;J. Oral Biosci.,2022 2. Preliminary Evaluation of Proliferation, Wound Healing Properties, Osteogenic and Chondrogenic Potential of Dental Pulp Stem Cells Obtained from Healthy and Periodontitis Affected Teeth;Fageeh;Cells,2021 3. Hagar, M.N., Yazid, F., Luchman, N.A., Ariffin, S.H.Z., and Wahab, R.M.A. (2021). Comparative evaluation of osteogenic differentiation potential of stem cells derived from dental pulp and exfoliated deciduous teeth cultured over granular hydroxyapatite based scaffold. BMC Oral Health, 21. 4. In vitro analysis of the influence of mineralized and EDTA-demineralized allogenous bone on the viability and differentiation of osteoblasts and dental pulp stem cells;Bertassoli;Cell Tissue Bank.,2020 5. Abidin, I.Z.Z., Manogaran, T., Abdul Wahab, R.M., Karsani, S.A., Yazid, M.D., Yazid, F., Ariffin, Z.Z., Johari, A.N., and Zainal Ariffin, S.H. (2022). Label-free quantitative proteomic analysis of ascorbic acid-induced differentially expressed osteoblast-related proteins in dental pulp stem cells from deciduous and permanent teeth. Curr. Stem Cell Res. Ther., ahead of print.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|