Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization

Background information. ADM (adrenomedullin) has pleiotropic effects, including regulation of inflammation, infection, angiogenesis, mineralized‐tissue formation and development. Recently, we demonstrated up‐regulation of the ADM transcript in diseased pulpal tissue while the protein is sequestered...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biology of the cell 2010-03, Vol.102 (3), p.145-157
Hauptverfasser: Musson, David S., McLachlan, Julia L., Sloan, Alastair J., Smith, Anthony J., Cooper, Paul R.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 157
container_issue 3
container_start_page 145
container_title Biology of the cell
container_volume 102
creator Musson, David S.
McLachlan, Julia L.
Sloan, Alastair J.
Smith, Anthony J.
Cooper, Paul R.
description Background information. ADM (adrenomedullin) has pleiotropic effects, including regulation of inflammation, infection, angiogenesis, mineralized‐tissue formation and development. Recently, we demonstrated up‐regulation of the ADM transcript in diseased pulpal tissue while the protein is sequestered within the dentine extracellular matrix during dentinogenesis. The present study aimed to characterize ADM localization during rodent dental tissue development and determine its potential effects on dental cells. Finally, we sought to profile ADM transcript levels in adult organs and tissues to compare its expression in teeth relative to other tissues. Results. Immunohistochemical analysis of developmental rat oral tissues indicated that, at E16 (embryonic day 16), ADM was present in dental epithelium and, by E18, ADM localized to the dental papilla and inner and outer dental epithelia. By E20, ADM was detected in secretory odontoblasts and ameloblasts and exhibited a similar expression profile to that of the key dentinogenesis signalling molecule, TGF‐β1 (transforming growth factor‐β1). Cell growth analysis in the dental MDPC‐23, OD‐21 and control 3T3 cell lines exposed to ADM (range 10−15–10−7 M) together with EDTA‐extracted DMPs (dentine matrix proteins) (range 0.00001–1000 mg/ml) containing comparable concentrations of ADM demonstrated that ADM stimulated a biphasic response in dental cell growth, comparable with that of DMPs, with peak stimulation observed at ∼10−11 M. For mineralization analysis, cell lines were exposed to combinations of 50 μg/ml ascorbic acid, 10 mM β‐G (β‐glycerophosphate), 10−8 M DEX (dexamethasone) and ADM (range 10−15–10−7 M). The results demonstrated that ADM could substitute for DEX to stimulate mineralization. Postnatally, multiple tissue expression profiling indicated abundant ADM levels in tongue and pulpal tissues. Conclusions. During oral and dental tissue development ADM initially localizes to epithelial tissue, whereas during later stages it is present in mineralized secreting cells, including odontoblasts. ADM may regulate proliferation and mineralization processes during development, whereas, in adulthood, it may be important for maintaining dental tissue homoeostasis.
doi_str_mv 10.1042/BC20090122
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_733683085</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>21406578</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4292-7d91d8742ff72df6fdb5f7537649a6fca1ddc6ea67021682588e21edc86981a83</originalsourceid><addsrcrecordid>eNp90UtP3DAQB3ALFcGWcukHqHwqUqWA7fiVIyxl-6BwoYKbZeIJdevEi52Ux6dvwq66Ny4eWfPTX6MZhN5TckgJZ0cnc0ZIRShjW2hGldRFydjNGzQjjOuCV4Tsorc5_yaE8EqLHbRLK800oWKG4rFL0MUW3BCC77DPGB6XCXIGh92QfHeHU3TQ9Xh6bMC9z3mA8fcXQly2U8d2Di9TbGMPGdcQAr5L8aH_9dJofQfJBv9sex-7d2i7sSHD_rruoZ9nn6_mX4rzy8XX-fF5UXNWsUK5ijqtOGsaxVwjG3crGiVKJXllZVNb6lwtwUpFGJWaCa2BUXC1lpWmVpd76GCVO851P0DuTevzNJrtIA7ZqLKUuiRajPLjq5JRTqRQU-SnFaxTzDlBY5bJtzY9GUrMdAizOcSIP6xTh9txuRu63vwIihV48AGeXokyJ5dzzjbe5x4e_3ub_hipSiXM9cXCfD_7diUWpz_MRfkP4Y-hYA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>21406578</pqid></control><display><type>article</type><title>Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Musson, David S. ; McLachlan, Julia L. ; Sloan, Alastair J. ; Smith, Anthony J. ; Cooper, Paul R.</creator><creatorcontrib>Musson, David S. ; McLachlan, Julia L. ; Sloan, Alastair J. ; Smith, Anthony J. ; Cooper, Paul R.</creatorcontrib><description>Background information. ADM (adrenomedullin) has pleiotropic effects, including regulation of inflammation, infection, angiogenesis, mineralized‐tissue formation and development. Recently, we demonstrated up‐regulation of the ADM transcript in diseased pulpal tissue while the protein is sequestered within the dentine extracellular matrix during dentinogenesis. The present study aimed to characterize ADM localization during rodent dental tissue development and determine its potential effects on dental cells. Finally, we sought to profile ADM transcript levels in adult organs and tissues to compare its expression in teeth relative to other tissues. Results. Immunohistochemical analysis of developmental rat oral tissues indicated that, at E16 (embryonic day 16), ADM was present in dental epithelium and, by E18, ADM localized to the dental papilla and inner and outer dental epithelia. By E20, ADM was detected in secretory odontoblasts and ameloblasts and exhibited a similar expression profile to that of the key dentinogenesis signalling molecule, TGF‐β1 (transforming growth factor‐β1). Cell growth analysis in the dental MDPC‐23, OD‐21 and control 3T3 cell lines exposed to ADM (range 10−15–10−7 M) together with EDTA‐extracted DMPs (dentine matrix proteins) (range 0.00001–1000 mg/ml) containing comparable concentrations of ADM demonstrated that ADM stimulated a biphasic response in dental cell growth, comparable with that of DMPs, with peak stimulation observed at ∼10−11 M. For mineralization analysis, cell lines were exposed to combinations of 50 μg/ml ascorbic acid, 10 mM β‐G (β‐glycerophosphate), 10−8 M DEX (dexamethasone) and ADM (range 10−15–10−7 M). The results demonstrated that ADM could substitute for DEX to stimulate mineralization. Postnatally, multiple tissue expression profiling indicated abundant ADM levels in tongue and pulpal tissues. Conclusions. During oral and dental tissue development ADM initially localizes to epithelial tissue, whereas during later stages it is present in mineralized secreting cells, including odontoblasts. ADM may regulate proliferation and mineralization processes during development, whereas, in adulthood, it may be important for maintaining dental tissue homoeostasis.</description><identifier>ISSN: 0248-4900</identifier><identifier>EISSN: 1768-322X</identifier><identifier>DOI: 10.1042/BC20090122</identifier><identifier>PMID: 19828015</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>adrenomedullin ; Adrenomedullin - genetics ; Adrenomedullin - metabolism ; Ameloblasts - cytology ; Ameloblasts - metabolism ; Animals ; Animals, Newborn ; Calcification, Physiologic - physiology ; Cell Differentiation - physiology ; Cell Line ; Cell Proliferation ; Dental Pulp - cytology ; Dental Pulp - growth &amp; development ; Dental Pulp - metabolism ; dental tissue regeneration ; dentine ; Epithelial Cells - cytology ; Epithelial Cells - metabolism ; Homeostasis - physiology ; Immunohistochemistry ; Male ; Mice ; Mouth - cytology ; Mouth - embryology ; NIH 3T3 Cells ; odontoblast ; Odontoblasts - cytology ; Odontoblasts - metabolism ; Rats ; Rats, Wistar ; reparative dentinogenesis ; RNA, Messenger - metabolism ; Tongue - cytology ; Tongue - growth &amp; development ; Tongue - metabolism ; Tooth - cytology ; Tooth - embryology</subject><ispartof>Biology of the cell, 2010-03, Vol.102 (3), p.145-157</ispartof><rights>2010 Société Française des Microscopies and Société Biologie Cellulaire de France</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4292-7d91d8742ff72df6fdb5f7537649a6fca1ddc6ea67021682588e21edc86981a83</citedby><cites>FETCH-LOGICAL-c4292-7d91d8742ff72df6fdb5f7537649a6fca1ddc6ea67021682588e21edc86981a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1042%2FBC20090122$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1042%2FBC20090122$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19828015$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Musson, David S.</creatorcontrib><creatorcontrib>McLachlan, Julia L.</creatorcontrib><creatorcontrib>Sloan, Alastair J.</creatorcontrib><creatorcontrib>Smith, Anthony J.</creatorcontrib><creatorcontrib>Cooper, Paul R.</creatorcontrib><title>Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization</title><title>Biology of the cell</title><addtitle>Biol Cell</addtitle><description>Background information. ADM (adrenomedullin) has pleiotropic effects, including regulation of inflammation, infection, angiogenesis, mineralized‐tissue formation and development. Recently, we demonstrated up‐regulation of the ADM transcript in diseased pulpal tissue while the protein is sequestered within the dentine extracellular matrix during dentinogenesis. The present study aimed to characterize ADM localization during rodent dental tissue development and determine its potential effects on dental cells. Finally, we sought to profile ADM transcript levels in adult organs and tissues to compare its expression in teeth relative to other tissues. Results. Immunohistochemical analysis of developmental rat oral tissues indicated that, at E16 (embryonic day 16), ADM was present in dental epithelium and, by E18, ADM localized to the dental papilla and inner and outer dental epithelia. By E20, ADM was detected in secretory odontoblasts and ameloblasts and exhibited a similar expression profile to that of the key dentinogenesis signalling molecule, TGF‐β1 (transforming growth factor‐β1). Cell growth analysis in the dental MDPC‐23, OD‐21 and control 3T3 cell lines exposed to ADM (range 10−15–10−7 M) together with EDTA‐extracted DMPs (dentine matrix proteins) (range 0.00001–1000 mg/ml) containing comparable concentrations of ADM demonstrated that ADM stimulated a biphasic response in dental cell growth, comparable with that of DMPs, with peak stimulation observed at ∼10−11 M. For mineralization analysis, cell lines were exposed to combinations of 50 μg/ml ascorbic acid, 10 mM β‐G (β‐glycerophosphate), 10−8 M DEX (dexamethasone) and ADM (range 10−15–10−7 M). The results demonstrated that ADM could substitute for DEX to stimulate mineralization. Postnatally, multiple tissue expression profiling indicated abundant ADM levels in tongue and pulpal tissues. Conclusions. During oral and dental tissue development ADM initially localizes to epithelial tissue, whereas during later stages it is present in mineralized secreting cells, including odontoblasts. ADM may regulate proliferation and mineralization processes during development, whereas, in adulthood, it may be important for maintaining dental tissue homoeostasis.</description><subject>adrenomedullin</subject><subject>Adrenomedullin - genetics</subject><subject>Adrenomedullin - metabolism</subject><subject>Ameloblasts - cytology</subject><subject>Ameloblasts - metabolism</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Calcification, Physiologic - physiology</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Line</subject><subject>Cell Proliferation</subject><subject>Dental Pulp - cytology</subject><subject>Dental Pulp - growth &amp; development</subject><subject>Dental Pulp - metabolism</subject><subject>dental tissue regeneration</subject><subject>dentine</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - metabolism</subject><subject>Homeostasis - physiology</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Mice</subject><subject>Mouth - cytology</subject><subject>Mouth - embryology</subject><subject>NIH 3T3 Cells</subject><subject>odontoblast</subject><subject>Odontoblasts - cytology</subject><subject>Odontoblasts - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>reparative dentinogenesis</subject><subject>RNA, Messenger - metabolism</subject><subject>Tongue - cytology</subject><subject>Tongue - growth &amp; development</subject><subject>Tongue - metabolism</subject><subject>Tooth - cytology</subject><subject>Tooth - embryology</subject><issn>0248-4900</issn><issn>1768-322X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90UtP3DAQB3ALFcGWcukHqHwqUqWA7fiVIyxl-6BwoYKbZeIJdevEi52Ux6dvwq66Ny4eWfPTX6MZhN5TckgJZ0cnc0ZIRShjW2hGldRFydjNGzQjjOuCV4Tsorc5_yaE8EqLHbRLK800oWKG4rFL0MUW3BCC77DPGB6XCXIGh92QfHeHU3TQ9Xh6bMC9z3mA8fcXQly2U8d2Di9TbGMPGdcQAr5L8aH_9dJofQfJBv9sex-7d2i7sSHD_rruoZ9nn6_mX4rzy8XX-fF5UXNWsUK5ijqtOGsaxVwjG3crGiVKJXllZVNb6lwtwUpFGJWaCa2BUXC1lpWmVpd76GCVO851P0DuTevzNJrtIA7ZqLKUuiRajPLjq5JRTqRQU-SnFaxTzDlBY5bJtzY9GUrMdAizOcSIP6xTh9txuRu63vwIihV48AGeXokyJ5dzzjbe5x4e_3ub_hipSiXM9cXCfD_7diUWpz_MRfkP4Y-hYA</recordid><startdate>201003</startdate><enddate>201003</enddate><creator>Musson, David S.</creator><creator>McLachlan, Julia L.</creator><creator>Sloan, Alastair J.</creator><creator>Smith, Anthony J.</creator><creator>Cooper, Paul R.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>201003</creationdate><title>Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization</title><author>Musson, David S. ; McLachlan, Julia L. ; Sloan, Alastair J. ; Smith, Anthony J. ; Cooper, Paul R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4292-7d91d8742ff72df6fdb5f7537649a6fca1ddc6ea67021682588e21edc86981a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>adrenomedullin</topic><topic>Adrenomedullin - genetics</topic><topic>Adrenomedullin - metabolism</topic><topic>Ameloblasts - cytology</topic><topic>Ameloblasts - metabolism</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Calcification, Physiologic - physiology</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Line</topic><topic>Cell Proliferation</topic><topic>Dental Pulp - cytology</topic><topic>Dental Pulp - growth &amp; development</topic><topic>Dental Pulp - metabolism</topic><topic>dental tissue regeneration</topic><topic>dentine</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - metabolism</topic><topic>Homeostasis - physiology</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Mice</topic><topic>Mouth - cytology</topic><topic>Mouth - embryology</topic><topic>NIH 3T3 Cells</topic><topic>odontoblast</topic><topic>Odontoblasts - cytology</topic><topic>Odontoblasts - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>reparative dentinogenesis</topic><topic>RNA, Messenger - metabolism</topic><topic>Tongue - cytology</topic><topic>Tongue - growth &amp; development</topic><topic>Tongue - metabolism</topic><topic>Tooth - cytology</topic><topic>Tooth - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Musson, David S.</creatorcontrib><creatorcontrib>McLachlan, Julia L.</creatorcontrib><creatorcontrib>Sloan, Alastair J.</creatorcontrib><creatorcontrib>Smith, Anthony J.</creatorcontrib><creatorcontrib>Cooper, Paul R.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Musson, David S.</au><au>McLachlan, Julia L.</au><au>Sloan, Alastair J.</au><au>Smith, Anthony J.</au><au>Cooper, Paul R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization</atitle><jtitle>Biology of the cell</jtitle><addtitle>Biol Cell</addtitle><date>2010-03</date><risdate>2010</risdate><volume>102</volume><issue>3</issue><spage>145</spage><epage>157</epage><pages>145-157</pages><issn>0248-4900</issn><eissn>1768-322X</eissn><abstract>Background information. ADM (adrenomedullin) has pleiotropic effects, including regulation of inflammation, infection, angiogenesis, mineralized‐tissue formation and development. Recently, we demonstrated up‐regulation of the ADM transcript in diseased pulpal tissue while the protein is sequestered within the dentine extracellular matrix during dentinogenesis. The present study aimed to characterize ADM localization during rodent dental tissue development and determine its potential effects on dental cells. Finally, we sought to profile ADM transcript levels in adult organs and tissues to compare its expression in teeth relative to other tissues. Results. Immunohistochemical analysis of developmental rat oral tissues indicated that, at E16 (embryonic day 16), ADM was present in dental epithelium and, by E18, ADM localized to the dental papilla and inner and outer dental epithelia. By E20, ADM was detected in secretory odontoblasts and ameloblasts and exhibited a similar expression profile to that of the key dentinogenesis signalling molecule, TGF‐β1 (transforming growth factor‐β1). Cell growth analysis in the dental MDPC‐23, OD‐21 and control 3T3 cell lines exposed to ADM (range 10−15–10−7 M) together with EDTA‐extracted DMPs (dentine matrix proteins) (range 0.00001–1000 mg/ml) containing comparable concentrations of ADM demonstrated that ADM stimulated a biphasic response in dental cell growth, comparable with that of DMPs, with peak stimulation observed at ∼10−11 M. For mineralization analysis, cell lines were exposed to combinations of 50 μg/ml ascorbic acid, 10 mM β‐G (β‐glycerophosphate), 10−8 M DEX (dexamethasone) and ADM (range 10−15–10−7 M). The results demonstrated that ADM could substitute for DEX to stimulate mineralization. Postnatally, multiple tissue expression profiling indicated abundant ADM levels in tongue and pulpal tissues. Conclusions. During oral and dental tissue development ADM initially localizes to epithelial tissue, whereas during later stages it is present in mineralized secreting cells, including odontoblasts. ADM may regulate proliferation and mineralization processes during development, whereas, in adulthood, it may be important for maintaining dental tissue homoeostasis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19828015</pmid><doi>10.1042/BC20090122</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0248-4900
ispartof Biology of the cell, 2010-03, Vol.102 (3), p.145-157
issn 0248-4900
1768-322X
language eng
recordid cdi_proquest_miscellaneous_733683085
source MEDLINE; Access via Wiley Online Library
subjects adrenomedullin
Adrenomedullin - genetics
Adrenomedullin - metabolism
Ameloblasts - cytology
Ameloblasts - metabolism
Animals
Animals, Newborn
Calcification, Physiologic - physiology
Cell Differentiation - physiology
Cell Line
Cell Proliferation
Dental Pulp - cytology
Dental Pulp - growth & development
Dental Pulp - metabolism
dental tissue regeneration
dentine
Epithelial Cells - cytology
Epithelial Cells - metabolism
Homeostasis - physiology
Immunohistochemistry
Male
Mice
Mouth - cytology
Mouth - embryology
NIH 3T3 Cells
odontoblast
Odontoblasts - cytology
Odontoblasts - metabolism
Rats
Rats, Wistar
reparative dentinogenesis
RNA, Messenger - metabolism
Tongue - cytology
Tongue - growth & development
Tongue - metabolism
Tooth - cytology
Tooth - embryology
title Adrenomedullin is expressed during rodent dental tissue development and promotes cell growth and mineralization
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T17%3A50%3A50IST&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=Adrenomedullin%20is%20expressed%20during%20rodent%20dental%20tissue%20development%20and%20promotes%20cell%20growth%20and%20mineralization&rft.jtitle=Biology%20of%20the%20cell&rft.au=Musson,%20David%20S.&rft.date=2010-03&rft.volume=102&rft.issue=3&rft.spage=145&rft.epage=157&rft.pages=145-157&rft.issn=0248-4900&rft.eissn=1768-322X&rft_id=info:doi/10.1042/BC20090122&rft_dat=%3Cproquest_cross%3E21406578%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=21406578&rft_id=info:pmid/19828015&rfr_iscdi=true