Dental Pulp Stem Cells: Advances to Applications

Takeo W Tsutsui Department of Pharmacology, School of Life Dentistry at Tokyo, The Nippon Dental University, Tokyo, JapanCorrespondence: Takeo W TsutsuiDepartment of Pharmacology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-Ku, Tokyo 102-8159, JapanTel +81...

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spelling oai:doaj.org-article:234bdf86097f49639bd11e1f1f674ead2021-12-02T07:31:24ZDental Pulp Stem Cells: Advances to Applications1178-6957https://doaj.org/article/234bdf86097f49639bd11e1f1f674ead2020-02-01T00:00:00Zhttps://www.dovepress.com/dental-pulp-stem-cells-advances-to-applications-peer-reviewed-article-SCCAAhttps://doaj.org/toc/1178-6957Takeo W Tsutsui Department of Pharmacology, School of Life Dentistry at Tokyo, The Nippon Dental University, Tokyo, JapanCorrespondence: Takeo W TsutsuiDepartment of Pharmacology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-Ku, Tokyo 102-8159, JapanTel +81 3-3261-8311Fax +81 3-3264-8399Email ryuryu@tky.ndu.ac.jpAbstract: Dental pulp stem cells (DPSCs) have a high capacity for differentiation and the ability to regenerate a dentin/pulp-like complex. Numerous studies have provided evidence of DPSCs’ differentiation capacity, such as in neurogenesis, adipogenesis, osteogenesis, chondrogenesis, angiogenesis, and dentinogenesis. The molecular mechanisms and functions of DPSCs’ differentiation process are affected by growth factors and scaffolds. For example, growth factors such as basic fibroblast growth factor (bFGF), transforming growth factor-β (TGF-β), nerve growth factor (NGF), platelet-derived growth factor (PDGF), and bone morphogenic proteins (BMPs) influence DPSC fate, including in differentiation, cell proliferation, and wound healing. In addition, several types of scaffolds, such as collagen, hydrogel, decellularized bioscaffold, and nanofibrous spongy microspheres, have been used to characterize DPSC cellular attachment, migration, proliferation, differentiation, and functions. An appropriate combination of growth factors and scaffolds can enhance the differentiation capacity of DPSCs, in terms of optimizing not only dental-related expression but also dental pulp morphology. For a cell-based clinical approach, focus has been placed on the tissue engineering triad [cells/bioactive molecules (growth factors)/scaffolds] to characterize DPSCs. It is clear that a deep understanding of the mechanisms of stem cells, including their aging, self-renewal, microenvironmental homeostasis, and differentiation correlated with cell activity, the energy for which is provided from mitochondria, should provide new approaches for DPSC research and therapeutics. Mitochondrial functions and dynamics are related to the direction of stem cell differentiation, including glycolysis, oxidative phosphorylation, mitochondrial metabolism, mitochondrial transcription factor A (TFAM), mitochondrial elongation, and mitochondrial fusion and fission proteins. This review summarizes the effects of major growth factors and scaffolds for regenerating dentin/pulp-like complexes, as well as elucidating mitochondrial properties of DPSCs for the development of advanced applications research.Keywords: dental pulp stem cell, bioactive molecule, growth factor, scaffold, mitochondria, regenerative therapyTsutsui TWDove Medical Pressarticledental pulp stem cellbioactive moleculegrowth factorscaffoldmitochondriaregenerative therapyCytologyQH573-671ENStem Cells and Cloning: Advances and Applications, Vol Volume 13, Pp 33-42 (2020)
institution DOAJ
collection DOAJ
language EN
topic dental pulp stem cell
bioactive molecule
growth factor
scaffold
mitochondria
regenerative therapy
Cytology
QH573-671
spellingShingle dental pulp stem cell
bioactive molecule
growth factor
scaffold
mitochondria
regenerative therapy
Cytology
QH573-671
Tsutsui TW
Dental Pulp Stem Cells: Advances to Applications
description Takeo W Tsutsui Department of Pharmacology, School of Life Dentistry at Tokyo, The Nippon Dental University, Tokyo, JapanCorrespondence: Takeo W TsutsuiDepartment of Pharmacology, The Nippon Dental University School of Life Dentistry at Tokyo, 1-9-20 Fujimi, Chiyoda-Ku, Tokyo 102-8159, JapanTel +81 3-3261-8311Fax +81 3-3264-8399Email ryuryu@tky.ndu.ac.jpAbstract: Dental pulp stem cells (DPSCs) have a high capacity for differentiation and the ability to regenerate a dentin/pulp-like complex. Numerous studies have provided evidence of DPSCs’ differentiation capacity, such as in neurogenesis, adipogenesis, osteogenesis, chondrogenesis, angiogenesis, and dentinogenesis. The molecular mechanisms and functions of DPSCs’ differentiation process are affected by growth factors and scaffolds. For example, growth factors such as basic fibroblast growth factor (bFGF), transforming growth factor-β (TGF-β), nerve growth factor (NGF), platelet-derived growth factor (PDGF), and bone morphogenic proteins (BMPs) influence DPSC fate, including in differentiation, cell proliferation, and wound healing. In addition, several types of scaffolds, such as collagen, hydrogel, decellularized bioscaffold, and nanofibrous spongy microspheres, have been used to characterize DPSC cellular attachment, migration, proliferation, differentiation, and functions. An appropriate combination of growth factors and scaffolds can enhance the differentiation capacity of DPSCs, in terms of optimizing not only dental-related expression but also dental pulp morphology. For a cell-based clinical approach, focus has been placed on the tissue engineering triad [cells/bioactive molecules (growth factors)/scaffolds] to characterize DPSCs. It is clear that a deep understanding of the mechanisms of stem cells, including their aging, self-renewal, microenvironmental homeostasis, and differentiation correlated with cell activity, the energy for which is provided from mitochondria, should provide new approaches for DPSC research and therapeutics. Mitochondrial functions and dynamics are related to the direction of stem cell differentiation, including glycolysis, oxidative phosphorylation, mitochondrial metabolism, mitochondrial transcription factor A (TFAM), mitochondrial elongation, and mitochondrial fusion and fission proteins. This review summarizes the effects of major growth factors and scaffolds for regenerating dentin/pulp-like complexes, as well as elucidating mitochondrial properties of DPSCs for the development of advanced applications research.Keywords: dental pulp stem cell, bioactive molecule, growth factor, scaffold, mitochondria, regenerative therapy
format article
author Tsutsui TW
author_facet Tsutsui TW
author_sort Tsutsui TW
title Dental Pulp Stem Cells: Advances to Applications
title_short Dental Pulp Stem Cells: Advances to Applications
title_full Dental Pulp Stem Cells: Advances to Applications
title_fullStr Dental Pulp Stem Cells: Advances to Applications
title_full_unstemmed Dental Pulp Stem Cells: Advances to Applications
title_sort dental pulp stem cells: advances to applications
publisher Dove Medical Press
publishDate 2020
url https://doaj.org/article/234bdf86097f49639bd11e1f1f674ead
work_keys_str_mv AT tsutsuitw dentalpulpstemcellsadvancestoapplications
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