Dental Pulp-Derived Mesenchymal Stem Cells for Modeling Genetic Disorders
A subpopulation of mesenchymal stem cells, developmentally derived from multipotent neural crest cells that form multiple facial tissues, resides within the dental pulp of human teeth. These stem cells show high proliferative capacity in vitro and are multipotent, including adipogenic, myogenic, ost...
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Published in | International journal of molecular sciences Vol. 22; no. 5; p. 2269 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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25.02.2021
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ISSN | 1422-0067 1661-6596 1422-0067 |
DOI | 10.3390/ijms22052269 |
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Abstract | A subpopulation of mesenchymal stem cells, developmentally derived from multipotent neural crest cells that form multiple facial tissues, resides within the dental pulp of human teeth. These stem cells show high proliferative capacity in vitro and are multipotent, including adipogenic, myogenic, osteogenic, chondrogenic, and neurogenic potential. Teeth containing viable cells are harvested via minimally invasive procedures, based on various clinical diagnoses, but then usually discarded as medical waste, indicating the relatively low ethical considerations to reuse these cells for medical applications. Previous studies have demonstrated that stem cells derived from healthy subjects are an excellent source for cell-based medicine, tissue regeneration, and bioengineering. Furthermore, stem cells donated by patients affected by genetic disorders can serve as in vitro models of disease-specific genetic variants, indicating additional applications of these stem cells with high plasticity. This review discusses the benefits, limitations, and perspectives of patient-derived dental pulp stem cells as alternatives that may complement other excellent, yet incomplete stem cell models, such as induced pluripotent stem cells, together with our recent data. |
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AbstractList | A subpopulation of mesenchymal stem cells, developmentally derived from multipotent neural crest cells that form multiple facial tissues, resides within the dental pulp of human teeth. These stem cells show high proliferative capacity in vitro and are multipotent, including adipogenic, myogenic, osteogenic, chondrogenic, and neurogenic potential. Teeth containing viable cells are harvested via minimally invasive procedures, based on various clinical diagnoses, but then usually discarded as medical waste, indicating the relatively low ethical considerations to reuse these cells for medical applications. Previous studies have demonstrated that stem cells derived from healthy subjects are an excellent source for cell-based medicine, tissue regeneration, and bioengineering. Furthermore, stem cells donated by patients affected by genetic disorders can serve as in vitro models of disease-specific genetic variants, indicating additional applications of these stem cells with high plasticity. This review discusses the benefits, limitations, and perspectives of patient-derived dental pulp stem cells as alternatives that may complement other excellent, yet incomplete stem cell models, such as induced pluripotent stem cells, together with our recent data. A subpopulation of mesenchymal stem cells, developmentally derived from multipotent neural crest cells that form multiple facial tissues, resides within the dental pulp of human teeth. These stem cells show high proliferative capacity in vitro and are multipotent, including adipogenic, myogenic, osteogenic, chondrogenic, and neurogenic potential. Teeth containing viable cells are harvested via minimally invasive procedures, based on various clinical diagnoses, but then usually discarded as medical waste, indicating the relatively low ethical considerations to reuse these cells for medical applications. Previous studies have demonstrated that stem cells derived from healthy subjects are an excellent source for cell-based medicine, tissue regeneration, and bioengineering. Furthermore, stem cells donated by patients affected by genetic disorders can serve as in vitro models of disease-specific genetic variants, indicating additional applications of these stem cells with high plasticity. This review discusses the benefits, limitations, and perspectives of patient-derived dental pulp stem cells as alternatives that may complement other excellent, yet incomplete stem cell models, such as induced pluripotent stem cells, together with our recent data.A subpopulation of mesenchymal stem cells, developmentally derived from multipotent neural crest cells that form multiple facial tissues, resides within the dental pulp of human teeth. These stem cells show high proliferative capacity in vitro and are multipotent, including adipogenic, myogenic, osteogenic, chondrogenic, and neurogenic potential. Teeth containing viable cells are harvested via minimally invasive procedures, based on various clinical diagnoses, but then usually discarded as medical waste, indicating the relatively low ethical considerations to reuse these cells for medical applications. Previous studies have demonstrated that stem cells derived from healthy subjects are an excellent source for cell-based medicine, tissue regeneration, and bioengineering. Furthermore, stem cells donated by patients affected by genetic disorders can serve as in vitro models of disease-specific genetic variants, indicating additional applications of these stem cells with high plasticity. This review discusses the benefits, limitations, and perspectives of patient-derived dental pulp stem cells as alternatives that may complement other excellent, yet incomplete stem cell models, such as induced pluripotent stem cells, together with our recent data. |
Author | Yamada, Aya Hirofuji, Yuta Fukumoto, Satoshi Zhang, Yu Masuda, Keiji Sun, Xiao Yamaza, Haruyoshi Kato, Hiroki Sato, Hiroshi Han, Xu |
AuthorAffiliation | 2 Department of Molecular Cell Biology and Oral Anatomy, Graduate School of Dental Science, Kyushu University, Maidashi 3-1-1, Higashi-Ku, Fukuoka 812-8582, Japan; kato@dent.kyushu-u.ac.jp 3 Division of Pediatric Dentistry, Department of Oral Health and Development Sciences, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8577, Japan; yamada-a@dent.tohoku.ac.jp 1 Section of Oral Medicine for Children, Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, Maidashi 3-1-1, Higashi-Ku, Fukuoka 812-8582, Japan; kan@dent.kyushu-u.ac.jp (X.H.); hisato@dent.kyushu-u.ac.jp (H.S.); zhangyu@dent.kyushu-u.ac.jp (Y.Z.); sunxiao1988@dent.kyushu-u.ac.jp (X.S.); hirofuji@dent.kyushu-u.ac.jp (Y.H.); hyamaza@dent.kyushu-u.ac.jp (H.Y.) |
AuthorAffiliation_xml | – name: 1 Section of Oral Medicine for Children, Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, Maidashi 3-1-1, Higashi-Ku, Fukuoka 812-8582, Japan; kan@dent.kyushu-u.ac.jp (X.H.); hisato@dent.kyushu-u.ac.jp (H.S.); zhangyu@dent.kyushu-u.ac.jp (Y.Z.); sunxiao1988@dent.kyushu-u.ac.jp (X.S.); hirofuji@dent.kyushu-u.ac.jp (Y.H.); hyamaza@dent.kyushu-u.ac.jp (H.Y.) – name: 2 Department of Molecular Cell Biology and Oral Anatomy, Graduate School of Dental Science, Kyushu University, Maidashi 3-1-1, Higashi-Ku, Fukuoka 812-8582, Japan; kato@dent.kyushu-u.ac.jp – name: 3 Division of Pediatric Dentistry, Department of Oral Health and Development Sciences, Graduate School of Dentistry, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8577, Japan; yamada-a@dent.tohoku.ac.jp |
Author_xml | – sequence: 1 givenname: Keiji surname: Masuda fullname: Masuda, Keiji – sequence: 2 givenname: Xu surname: Han fullname: Han, Xu – sequence: 3 givenname: Hiroki surname: Kato fullname: Kato, Hiroki – sequence: 4 givenname: Hiroshi surname: Sato fullname: Sato, Hiroshi – sequence: 5 givenname: Yu surname: Zhang fullname: Zhang, Yu – sequence: 6 givenname: Xiao surname: Sun fullname: Sun, Xiao – sequence: 7 givenname: Yuta orcidid: 0000-0003-1138-3943 surname: Hirofuji fullname: Hirofuji, Yuta – sequence: 8 givenname: Haruyoshi surname: Yamaza fullname: Yamaza, Haruyoshi – sequence: 9 givenname: Aya surname: Yamada fullname: Yamada, Aya – sequence: 10 givenname: Satoshi surname: Fukumoto fullname: Fukumoto, Satoshi |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33668763$$D View this record in MEDLINE/PubMed |
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Keywords | stem cells from human exfoliated deciduous teeth mesenchymal stem cells dental pulp stem cells disease model |
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SubjectTerms | Apoptosis Cell Differentiation Congenital diseases Dental pulp Dental Pulp - cytology Disease Genetic Diseases, Inborn - pathology Genetic disorders Humans Medical research Mesenchymal Stem Cells - cytology Models, Biological Neurons Physiology Review Stem cells Teeth Tissue engineering |
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