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...
Gespeichert in:
Veröffentlicht in: | Orthodontics & craniofacial research 2021-11, Vol.24 (4), p.494-501 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 501 |
---|---|
container_issue | 4 |
container_start_page | 494 |
container_title | Orthodontics & craniofacial research |
container_volume | 24 |
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. |
doi_str_mv | 10.1111/ocr.12475 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2487152798</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2582373761</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3535-c96eb8d454ece60d9fe88d61d6aca490bac515f5d35693c9ba4f659edb993b503</originalsourceid><addsrcrecordid>eNp1kbtOHDEUhq0oKNxS5AWQpTRQLNjjy4zLaMUlEhJSgNryeM4khvF4sT2JtqOj5Rl5Ekx22SJS3Nj69fnzkX-EvlByTMs6CTYe04rX4gPaoZLQmWScfdycmdhGuyndEVKRqpKf0HaJOOF1s4OeriGGHEY3YhvGHF07ZUg4B5x_AS7pb5djwIsYuslmF0Ycemxw64J3HrKzGEbjYXh5fB7cPWBvMkRnBtzH4HGEcvFnNN5Dh0MsMSxcEQ9vxD1Ek90Y7LK8uI-2ejMk-Lze99Dt2enN_GJ2eXX-ff7tcmaZYGJmlYS26bjgYEGSTvXQNJ2knTTWcEVaYwUVveiYkIpZ1RreS6Gga5VirSBsDx2uvGWwhwlS1t4lC8NgRghT0hVvaiqqWjUF_foPehemOJbpdCWaitWslrRQRyvKxpBShF4vovMmLjUl-q0dXdrRf9sp7MHaOLXlRzbkex0FOFkBf9wAy_-b9NX8x0r5Ch4jnVs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2582373761</pqid></control><display><type>article</type><title>Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Bazina, Fayrouz ; Brouxhon, Sabine M. ; Graham, Uschi M. ; Kyrkanides, Stephanos</creator><creatorcontrib>Bazina, Fayrouz ; Brouxhon, Sabine M. ; Graham, Uschi M. ; Kyrkanides, Stephanos</creatorcontrib><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.</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 & craniofacial research, 2021-11, Vol.24 (4), p.494-501</ispartof><rights>2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2021 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-c96eb8d454ece60d9fe88d61d6aca490bac515f5d35693c9ba4f659edb993b503</citedby><cites>FETCH-LOGICAL-c3535-c96eb8d454ece60d9fe88d61d6aca490bac515f5d35693c9ba4f659edb993b503</cites><orcidid>0000-0002-2195-2751</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Focr.12475$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Focr.12475$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33540478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bazina, Fayrouz</creatorcontrib><creatorcontrib>Brouxhon, Sabine M.</creatorcontrib><creatorcontrib>Graham, Uschi M.</creatorcontrib><creatorcontrib>Kyrkanides, Stephanos</creatorcontrib><title>Serotonin contributes to the in vitro production of a biomimetic enamel‐like material from reprogrammed oral epithelial keratinocytes</title><title>Orthodontics & craniofacial research</title><addtitle>Orthod Craniofac Res</addtitle><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.</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 & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Orthodontics & 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 & 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. 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.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33540478</pmid><doi>10.1111/ocr.12475</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2195-2751</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1601-6335 |
ispartof | Orthodontics & craniofacial research, 2021-11, Vol.24 (4), p.494-501 |
issn | 1601-6335 1601-6343 |
language | eng |
recordid | cdi_proquest_miscellaneous_2487152798 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T16%3A19%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Serotonin%20contributes%20to%20the%20in%20vitro%20production%20of%20a%20biomimetic%20enamel%E2%80%90like%20material%20from%20reprogrammed%20oral%20epithelial%20keratinocytes&rft.jtitle=Orthodontics%20&%20craniofacial%20research&rft.au=Bazina,%20Fayrouz&rft.date=2021-11&rft.volume=24&rft.issue=4&rft.spage=494&rft.epage=501&rft.pages=494-501&rft.issn=1601-6335&rft.eissn=1601-6343&rft_id=info:doi/10.1111/ocr.12475&rft_dat=%3Cproquest_cross%3E2582373761%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2582373761&rft_id=info:pmid/33540478&rfr_iscdi=true |