1.Oral epithelial stem cells in tissue maintenance and disease: the first steps in a long journey.
International Journal of Oral Science 2013;5(3):121-129
The identification and characterization of stem cells is a major focus of developmental biology and regenerative medicine. The advent of genetic inducible fate mapping techniques has made it possible to precisely label specific cell populations and to follow their progeny over time. When combined with advanced mathematical and statistical methods, stem cell division dynamics can be studied in new and exciting ways. Despite advances in a number of tissues, relatively little attention has been paid to stem cells in the oral epithelium. This review will focus on current knowledge about adult oral epithelial stem cells, paradigms in other epithelial stem cell systems that could facilitate new discoveries in this area and the potential roles of epithelial stem cells in oral disease.
Adult Stem Cells
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cytology
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physiology
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Animals
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Asymmetric Cell Division
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Biomarkers
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Cell Proliferation
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Clone Cells
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Epithelial Cells
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cytology
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Genetic Drift
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Humans
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Mouth Mucosa
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cytology
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Mouth Neoplasms
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pathology
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Neoplastic Stem Cells
2.Adult dental epithelial stem cell-derived organoids deposit hydroxylapatite biomineral.
Hyun-Yi KIM ; Victoria COOLEY ; Eun-Jung KIM ; Shujin LI ; Jong-Min LEE ; Dina SHEYFER ; Wenjun LIU ; Ophir D KLEIN ; Derk JOESTER ; Han-Sung JUNG
International Journal of Oral Science 2023;15(1):55-55
Ameloblasts are specialized cells derived from the dental epithelium that produce enamel, a hierarchically structured tissue comprised of highly elongated hydroxylapatite (OHAp) crystallites. The unique function of the epithelial cells synthesizing crystallites and assembling them in a mechanically robust structure is not fully elucidated yet, partly due to limitations with in vitro experimental models. Herein, we demonstrate the ability to generate mineralizing dental epithelial organoids (DEOs) from adult dental epithelial stem cells (aDESCs) isolated from mouse incisor tissues. DEOs expressed ameloblast markers, could be maintained for more than five months (11 passages) in vitro in media containing modulators of Wnt, Egf, Bmp, Fgf and Notch signaling pathways, and were amenable to cryostorage. When transplanted underneath murine kidney capsules, organoids produced OHAp crystallites similar in composition, size, and shape to mineralized dental tissues, including some enamel-like elongated crystals. DEOs are thus a powerful in vitro model to study mineralization process by dental epithelium, which can pave the way to understanding amelogenesis and developing regenerative therapy of enamel.
Mice
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Animals
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Durapatite/metabolism*
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Dental Enamel/metabolism*
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Ameloblasts/metabolism*
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Amelogenesis
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Stem Cells
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Organoids