Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation

Background: Amelogenesis, the formation of dental enamel, is well understood at the histomorphological level but the underlying molecular mechanisms are poorly characterized. Ameloblasts secrete enamel matrix proteins and Ca2+, and also regulate extracellular pH as the formation of hydroxyapatite cr...

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Main Authors: Anna Földes, Thanyaporn Sang-Ngoen, Kristóf Kádár, Róbert Rácz, Ákos Zsembery, Pamela DenBesten, Martin C. Steward, Gábor Varga
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.682654/full
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spelling doaj-ad84152dbb0c4c8daa5004c8b905f7de2021-06-02T06:47:32ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-06-011210.3389/fphar.2021.682654682654Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel FormationAnna Földes0Thanyaporn Sang-Ngoen1Kristóf Kádár2Róbert Rácz3Ákos Zsembery4Pamela DenBesten5Martin C. Steward6Martin C. Steward7Gábor Varga8Department of Oral Biology, Semmelweis University, Budapest, HungaryDepartment of Oral Biology, Semmelweis University, Budapest, HungaryDepartment of Oral Biology, Semmelweis University, Budapest, HungaryDepartment of Oral Biology, Semmelweis University, Budapest, HungaryDepartment of Oral Biology, Semmelweis University, Budapest, HungaryDepartment of Orofacial Sciences, University of California San Francisco, San Francisco, CA, United StatesDepartment of Oral Biology, Semmelweis University, Budapest, HungarySchool of Medical Sciences, University of Manchester, Manchester, United KingdomDepartment of Oral Biology, Semmelweis University, Budapest, HungaryBackground: Amelogenesis, the formation of dental enamel, is well understood at the histomorphological level but the underlying molecular mechanisms are poorly characterized. Ameloblasts secrete enamel matrix proteins and Ca2+, and also regulate extracellular pH as the formation of hydroxyapatite crystals generates large quantities of protons. Genetic or environmental impairment of transport and regulatory processes (e.g. dental fluorosis) leads to the development of enamel defects such as hypomineralization.Aims: Our aims were to optimize the culture conditions for the three-dimensional growth of ameloblast-derived HAT-7 cells and to test the effects of fluoride exposure on HAT-7 spheroid formation.Methods: To generate 3D HAT-7 structures, cells were dispersed and plated within a Matrigel extracellular matrix scaffold and incubated in three different culture media. Spheroid formation was then monitored over a two-week period. Ion transporter and tight-junction protein expression was investigated by RT-qPCR. Intracellular Ca2+ and pH changes were measured by microfluorometry using the fluorescent dyes fura-2 and BCECF.Results: A combination of Hepato-STIM epithelial cell differentiation medium and Matrigel induced the expansion and formation of 3D HAT-7 spheroids. The cells retained their epithelial cell morphology and continued to express both ameloblast-specific and ion transport-specific marker genes. Furthermore, like two-dimensional HAT-7 monolayers, the HAT-7 spheroids were able to regulate their intracellular pH and to show intracellular calcium responses to extracellular stimulation. Finally, we demonstrated that HAT-7 spheroids may serve as a disease model for studying the effects of fluoride exposure during amelogenesis.Conclusion: In conclusion, HAT-7 cells cultivated within a Matrigel extracellular matrix form three-dimensional, multi-cellular, spheroidal structures that retain their functional capacity for pH regulation and intracellular Ca2+ signaling. This new 3D model will allow us to gain a better understanding of the molecular mechanisms involved in amelogenesis, not only in health but also in disorders of enamel formation, such as those resulting from fluoride exposure.https://www.frontiersin.org/articles/10.3389/fphar.2021.682654/fullHAT-7ameloblastamelogenesisbicarbonate transportintracellular pHcalcium signaling
collection DOAJ
language English
format Article
sources DOAJ
author Anna Földes
Thanyaporn Sang-Ngoen
Kristóf Kádár
Róbert Rácz
Ákos Zsembery
Pamela DenBesten
Martin C. Steward
Martin C. Steward
Gábor Varga
spellingShingle Anna Földes
Thanyaporn Sang-Ngoen
Kristóf Kádár
Róbert Rácz
Ákos Zsembery
Pamela DenBesten
Martin C. Steward
Martin C. Steward
Gábor Varga
Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
Frontiers in Pharmacology
HAT-7
ameloblast
amelogenesis
bicarbonate transport
intracellular pH
calcium signaling
author_facet Anna Földes
Thanyaporn Sang-Ngoen
Kristóf Kádár
Róbert Rácz
Ákos Zsembery
Pamela DenBesten
Martin C. Steward
Martin C. Steward
Gábor Varga
author_sort Anna Földes
title Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
title_short Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
title_full Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
title_fullStr Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
title_full_unstemmed Three-Dimensional Culture of Ameloblast-Originated HAT-7 Cells for Functional Modeling of Defective Tooth Enamel Formation
title_sort three-dimensional culture of ameloblast-originated hat-7 cells for functional modeling of defective tooth enamel formation
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2021-06-01
description Background: Amelogenesis, the formation of dental enamel, is well understood at the histomorphological level but the underlying molecular mechanisms are poorly characterized. Ameloblasts secrete enamel matrix proteins and Ca2+, and also regulate extracellular pH as the formation of hydroxyapatite crystals generates large quantities of protons. Genetic or environmental impairment of transport and regulatory processes (e.g. dental fluorosis) leads to the development of enamel defects such as hypomineralization.Aims: Our aims were to optimize the culture conditions for the three-dimensional growth of ameloblast-derived HAT-7 cells and to test the effects of fluoride exposure on HAT-7 spheroid formation.Methods: To generate 3D HAT-7 structures, cells were dispersed and plated within a Matrigel extracellular matrix scaffold and incubated in three different culture media. Spheroid formation was then monitored over a two-week period. Ion transporter and tight-junction protein expression was investigated by RT-qPCR. Intracellular Ca2+ and pH changes were measured by microfluorometry using the fluorescent dyes fura-2 and BCECF.Results: A combination of Hepato-STIM epithelial cell differentiation medium and Matrigel induced the expansion and formation of 3D HAT-7 spheroids. The cells retained their epithelial cell morphology and continued to express both ameloblast-specific and ion transport-specific marker genes. Furthermore, like two-dimensional HAT-7 monolayers, the HAT-7 spheroids were able to regulate their intracellular pH and to show intracellular calcium responses to extracellular stimulation. Finally, we demonstrated that HAT-7 spheroids may serve as a disease model for studying the effects of fluoride exposure during amelogenesis.Conclusion: In conclusion, HAT-7 cells cultivated within a Matrigel extracellular matrix form three-dimensional, multi-cellular, spheroidal structures that retain their functional capacity for pH regulation and intracellular Ca2+ signaling. This new 3D model will allow us to gain a better understanding of the molecular mechanisms involved in amelogenesis, not only in health but also in disorders of enamel formation, such as those resulting from fluoride exposure.
topic HAT-7
ameloblast
amelogenesis
bicarbonate transport
intracellular pH
calcium signaling
url https://www.frontiersin.org/articles/10.3389/fphar.2021.682654/full
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