Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes

Objectives To evaluate the role of serotonin in the development of a biomimetic enamel‐like material in vitro. Setting and Sample population Immortalized murine oral keratinocytes raised from adult mouse mucosa were cultured in vitro. In addition, specimens incorporating molar tooth buds harvested f...

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Veröffentlicht in:Orthodontics & craniofacial research 2021-11, Vol.24 (4), p.494-501
Hauptverfasser: Bazina, Fayrouz, Brouxhon, Sabine M., Graham, Uschi M., Kyrkanides, Stephanos
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creator Bazina, Fayrouz
Brouxhon, Sabine M.
Graham, Uschi M.
Kyrkanides, Stephanos
description Objectives To evaluate the role of serotonin in the development of a biomimetic enamel‐like material in vitro. Setting and Sample population Immortalized murine oral keratinocytes raised from adult mouse mucosa were cultured in vitro. In addition, specimens incorporating molar tooth buds harvested from mice were included in our studies. Materials and Methods We used cell‐based scaffold‐free tissue engineering to assemble three‐dimensional (3D) organoids into complex tissue constructs that closely emulate the complexity of adult enamel. We also analysed mouse molar specimens using immunohistochemistry for serotonin expression as well as its cognate receptor. Results TGF‐β1–reprogrammed murine oral keratinocytes formed organoids that laid down an amelogenin‐rich protein matrix when grown as three‐dimensional (3D) cultures in the presence of serotonin. Following mineralization, the newly formed crystals were densified under pressure and vacuum to produce a biomimetic enamel‐like material that demonstrated parallel alignment of hydroxyapatite crystals with some interspaced residual organoid matter into enamel prism‐like structures conferring size, mechanical properties comparable to tooth enamel, including light translucency. Serotonin expression was localized by immunohistochemistry proximal to the enamel organ of developing molar buds. Moreover, serotonin HTRb2 receptor expression was localized on ameloblasts within the enamel organ proximal to the area where serotonin was immunolocalized. Conclusions Our results demonstrate that serotonin is inductive in the development of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes in vitro. The facileness of harvesting adult somatic cells together with the versatility of our approach offers exciting opportunities to address regenerative challenges linked to lost enamel.
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Setting and Sample population Immortalized murine oral keratinocytes raised from adult mouse mucosa were cultured in vitro. In addition, specimens incorporating molar tooth buds harvested from mice were included in our studies. Materials and Methods We used cell‐based scaffold‐free tissue engineering to assemble three‐dimensional (3D) organoids into complex tissue constructs that closely emulate the complexity of adult enamel. We also analysed mouse molar specimens using immunohistochemistry for serotonin expression as well as its cognate receptor. Results TGF‐β1–reprogrammed murine oral keratinocytes formed organoids that laid down an amelogenin‐rich protein matrix when grown as three‐dimensional (3D) cultures in the presence of serotonin. Following mineralization, the newly formed crystals were densified under pressure and vacuum to produce a biomimetic enamel‐like material that demonstrated parallel alignment of hydroxyapatite crystals with some interspaced residual organoid matter into enamel prism‐like structures conferring size, mechanical properties comparable to tooth enamel, including light translucency. Serotonin expression was localized by immunohistochemistry proximal to the enamel organ of developing molar buds. Moreover, serotonin HTRb2 receptor expression was localized on ameloblasts within the enamel organ proximal to the area where serotonin was immunolocalized. Conclusions Our results demonstrate that serotonin is inductive in the development of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes in vitro. The facileness of harvesting adult somatic cells together with the versatility of our approach offers exciting opportunities to address regenerative challenges linked to lost enamel.</description><identifier>ISSN: 1601-6335</identifier><identifier>EISSN: 1601-6343</identifier><identifier>DOI: 10.1111/ocr.12475</identifier><identifier>PMID: 33540478</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Ameloblasts ; bioengineering ; Crystals ; Dental enamel ; Dentistry ; Enamel ; Hydroxyapatite ; Immunohistochemistry ; Keratinocytes ; Mechanical properties ; Mineralization ; Mucosa ; oral epithelium ; Organoids ; Serotonin ; Somatic cells ; Teeth ; TGFβ ; Tissue engineering</subject><ispartof>Orthodontics &amp; craniofacial research, 2021-11, Vol.24 (4), p.494-501</ispartof><rights>2021 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2021 John Wiley &amp; Sons A/S. 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Setting and Sample population Immortalized murine oral keratinocytes raised from adult mouse mucosa were cultured in vitro. In addition, specimens incorporating molar tooth buds harvested from mice were included in our studies. Materials and Methods We used cell‐based scaffold‐free tissue engineering to assemble three‐dimensional (3D) organoids into complex tissue constructs that closely emulate the complexity of adult enamel. We also analysed mouse molar specimens using immunohistochemistry for serotonin expression as well as its cognate receptor. Results TGF‐β1–reprogrammed murine oral keratinocytes formed organoids that laid down an amelogenin‐rich protein matrix when grown as three‐dimensional (3D) cultures in the presence of serotonin. Following mineralization, the newly formed crystals were densified under pressure and vacuum to produce a biomimetic enamel‐like material that demonstrated parallel alignment of hydroxyapatite crystals with some interspaced residual organoid matter into enamel prism‐like structures conferring size, mechanical properties comparable to tooth enamel, including light translucency. Serotonin expression was localized by immunohistochemistry proximal to the enamel organ of developing molar buds. Moreover, serotonin HTRb2 receptor expression was localized on ameloblasts within the enamel organ proximal to the area where serotonin was immunolocalized. Conclusions Our results demonstrate that serotonin is inductive in the development of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes in vitro. The facileness of harvesting adult somatic cells together with the versatility of our approach offers exciting opportunities to address regenerative challenges linked to lost enamel.</description><subject>Ameloblasts</subject><subject>bioengineering</subject><subject>Crystals</subject><subject>Dental enamel</subject><subject>Dentistry</subject><subject>Enamel</subject><subject>Hydroxyapatite</subject><subject>Immunohistochemistry</subject><subject>Keratinocytes</subject><subject>Mechanical properties</subject><subject>Mineralization</subject><subject>Mucosa</subject><subject>oral epithelium</subject><subject>Organoids</subject><subject>Serotonin</subject><subject>Somatic cells</subject><subject>Teeth</subject><subject>TGFβ</subject><subject>Tissue engineering</subject><issn>1601-6335</issn><issn>1601-6343</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kbtOHDEUhq0oKNxS5AWQpTRQLNjjy4zLaMUlEhJSgNryeM4khvF4sT2JtqOj5Rl5Ekx22SJS3Nj69fnzkX-EvlByTMs6CTYe04rX4gPaoZLQmWScfdycmdhGuyndEVKRqpKf0HaJOOF1s4OeriGGHEY3YhvGHF07ZUg4B5x_AS7pb5djwIsYuslmF0Ycemxw64J3HrKzGEbjYXh5fB7cPWBvMkRnBtzH4HGEcvFnNN5Dh0MsMSxcEQ9vxD1Ek90Y7LK8uI-2ejMk-Lze99Dt2enN_GJ2eXX-ff7tcmaZYGJmlYS26bjgYEGSTvXQNJ2knTTWcEVaYwUVveiYkIpZ1RreS6Gga5VirSBsDx2uvGWwhwlS1t4lC8NgRghT0hVvaiqqWjUF_foPehemOJbpdCWaitWslrRQRyvKxpBShF4vovMmLjUl-q0dXdrRf9sp7MHaOLXlRzbkex0FOFkBf9wAy_-b9NX8x0r5Ch4jnVs</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Bazina, Fayrouz</creator><creator>Brouxhon, Sabine M.</creator><creator>Graham, Uschi M.</creator><creator>Kyrkanides, Stephanos</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2195-2751</orcidid></search><sort><creationdate>202111</creationdate><title>Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes</title><author>Bazina, Fayrouz ; Brouxhon, Sabine M. ; Graham, Uschi M. ; Kyrkanides, Stephanos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-c96eb8d454ece60d9fe88d61d6aca490bac515f5d35693c9ba4f659edb993b503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ameloblasts</topic><topic>bioengineering</topic><topic>Crystals</topic><topic>Dental enamel</topic><topic>Dentistry</topic><topic>Enamel</topic><topic>Hydroxyapatite</topic><topic>Immunohistochemistry</topic><topic>Keratinocytes</topic><topic>Mechanical properties</topic><topic>Mineralization</topic><topic>Mucosa</topic><topic>oral epithelium</topic><topic>Organoids</topic><topic>Serotonin</topic><topic>Somatic cells</topic><topic>Teeth</topic><topic>TGFβ</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bazina, Fayrouz</creatorcontrib><creatorcontrib>Brouxhon, Sabine M.</creatorcontrib><creatorcontrib>Graham, Uschi M.</creatorcontrib><creatorcontrib>Kyrkanides, Stephanos</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Orthodontics &amp; craniofacial research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bazina, Fayrouz</au><au>Brouxhon, Sabine M.</au><au>Graham, Uschi M.</au><au>Kyrkanides, Stephanos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes</atitle><jtitle>Orthodontics &amp; craniofacial research</jtitle><addtitle>Orthod Craniofac Res</addtitle><date>2021-11</date><risdate>2021</risdate><volume>24</volume><issue>4</issue><spage>494</spage><epage>501</epage><pages>494-501</pages><issn>1601-6335</issn><eissn>1601-6343</eissn><abstract>Objectives To evaluate the role of serotonin in the development of a biomimetic enamel‐like material in vitro. Setting and Sample population Immortalized murine oral keratinocytes raised from adult mouse mucosa were cultured in vitro. In addition, specimens incorporating molar tooth buds harvested from mice were included in our studies. Materials and Methods We used cell‐based scaffold‐free tissue engineering to assemble three‐dimensional (3D) organoids into complex tissue constructs that closely emulate the complexity of adult enamel. We also analysed mouse molar specimens using immunohistochemistry for serotonin expression as well as its cognate receptor. Results TGF‐β1–reprogrammed murine oral keratinocytes formed organoids that laid down an amelogenin‐rich protein matrix when grown as three‐dimensional (3D) cultures in the presence of serotonin. Following mineralization, the newly formed crystals were densified under pressure and vacuum to produce a biomimetic enamel‐like material that demonstrated parallel alignment of hydroxyapatite crystals with some interspaced residual organoid matter into enamel prism‐like structures conferring size, mechanical properties comparable to tooth enamel, including light translucency. Serotonin expression was localized by immunohistochemistry proximal to the enamel organ of developing molar buds. Moreover, serotonin HTRb2 receptor expression was localized on ameloblasts within the enamel organ proximal to the area where serotonin was immunolocalized. Conclusions Our results demonstrate that serotonin is inductive in the development of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes in vitro. 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source Wiley Online Library Journals Frontfile Complete
subjects Ameloblasts
bioengineering
Crystals
Dental enamel
Dentistry
Enamel
Hydroxyapatite
Immunohistochemistry
Keratinocytes
Mechanical properties
Mineralization
Mucosa
oral epithelium
Organoids
Serotonin
Somatic cells
Teeth
TGFβ
Tissue engineering
title Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes
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