Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone Growth and Mineralization

ABSTRACT Matrix molecules such as the enamel‐related calcium‐binding phosphoprotein ameloblastin (AMBN) are expressed in multiple tissues, including teeth, bones, and cartilage. Here we have asked whether AMBN is of functional importance for timely long bone development and, if so, how it exerts its...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of bone and mineral research 2016-06, Vol.31 (6), p.1235-1246
Hauptverfasser: Lu, Xuanyu, Fukumoto, Satoshi, Yamada, Yoshihiko, Evans, Carla A, Diekwisch, Thomas GH, Luan, Xianghong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1246
container_issue 6
container_start_page 1235
container_title Journal of bone and mineral research
container_volume 31
creator Lu, Xuanyu
Fukumoto, Satoshi
Yamada, Yoshihiko
Evans, Carla A
Diekwisch, Thomas GH
Luan, Xianghong
description ABSTRACT Matrix molecules such as the enamel‐related calcium‐binding phosphoprotein ameloblastin (AMBN) are expressed in multiple tissues, including teeth, bones, and cartilage. Here we have asked whether AMBN is of functional importance for timely long bone development and, if so, how it exerts its function related to osteogenesis. Adolescent AMBN‐deficient mice (AMBNΔ5–6) suffered from a 33% to 38% reduction in femur length and an 8.4% shorter trunk spinal column when compared with WT controls, whereas there was no difference between adult animals. On a cellular level, AMBN truncation resulted in a shortened growth plate and a 41% to 49% reduction in the number of proliferating tibia chondrocytes and osteoblasts. Bone marrow stromal cells (BMSCs) isolated from AMBN mutant mice displayed defects in proliferation and differentiation potential as well as cytoskeleton organization. Osteogenesis‐related growth factors, such as insulin‐like growth factor 1 (IGF1) and BMP7, were also significantly (46% to 73%) reduced in AMBN‐deficient BMSCs. Addition of exogenous AMBN restored cytoskeleton structures in AMBN mutant BMSCs and resulted in a dramatic 400% to 600% increase in BMP2, BMP7, and Col1A expression. Block of RhoA diminished the effect of AMBN on osteogenic growth factor and matrix protein gene expression. Addition of exogenous BMP7 and IGF1 rescued the proliferation and differentiation potential of AMBN‐deficient BMSCs. Confirming the effects of AMBN on long bone growth, back‐crossing of mutant mice with full‐length AMBN overexpressors resulted in a complete rescue of AMBNΔ5–6 bone defects. Together, these data indicate that AMBN affects extracellular matrix production and cell adhesion properties in the long bone growth plate, resulting in altered cytoskeletal dynamics, increased osteogenesis‐related gene expression, as well as osteoblast and chondrocyte proliferation. We propose that AMBN facilitates rapid long bone growth and an important growth spurt during the skeletogenesis of adolescent tooth‐bearing vertebrates. © 2016 American Society for Bone and Mineral Research.
doi_str_mv 10.1002/jbmr.2788
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808731803</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4074843901</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4878-879778b44a28af0dcdbdb9cc89840320ee326fb6f79a9739374c4bcb746e06fc3</originalsourceid><addsrcrecordid>eNqF0UFLwzAUB_AgipvTg19ACl4UrEuaLEmPc8ypbCiiFy8lSVPtaBNNWrb56W236UEQL-9dfu8Pjz8AxwheIgij_lyW7jJinO-ALhpEOCSUo13QhZyTEBKMOuDA-zmEkA4o3QediDJKEUJd8DIsdWFlIXyVm4tAmGC8rJxQuijqQrhgJiqXL4MHZyvdgmGWaVX5YGrNa3BljQ4mzi6qt-YyDWa50U4U-aeocmsOwV4mCq-PtrsHnq_HT6ObcHo_uR0Np6EinPGQs5gxLgkRERcZTFUqUxkrxWNOII6g1jiimaQZi0XMcIwZUUQqyQjVkGYK98DZJvfd2Y9a-yopc98-IIy2tU8Qh5zhZuL_KYtxjCBisKGnv-jc1s40j6wVopxT1KjzjVLOeu90lry7vBRulSCYtN0kbTdJ201jT7aJtSx1-iO_y2hAfwMWeaFXfycld1ezx3XkF7Yxl8c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1793168861</pqid></control><display><type>article</type><title>Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone Growth and Mineralization</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Lu, Xuanyu ; Fukumoto, Satoshi ; Yamada, Yoshihiko ; Evans, Carla A ; Diekwisch, Thomas GH ; Luan, Xianghong</creator><creatorcontrib>Lu, Xuanyu ; Fukumoto, Satoshi ; Yamada, Yoshihiko ; Evans, Carla A ; Diekwisch, Thomas GH ; Luan, Xianghong</creatorcontrib><description>ABSTRACT Matrix molecules such as the enamel‐related calcium‐binding phosphoprotein ameloblastin (AMBN) are expressed in multiple tissues, including teeth, bones, and cartilage. Here we have asked whether AMBN is of functional importance for timely long bone development and, if so, how it exerts its function related to osteogenesis. Adolescent AMBN‐deficient mice (AMBNΔ5–6) suffered from a 33% to 38% reduction in femur length and an 8.4% shorter trunk spinal column when compared with WT controls, whereas there was no difference between adult animals. On a cellular level, AMBN truncation resulted in a shortened growth plate and a 41% to 49% reduction in the number of proliferating tibia chondrocytes and osteoblasts. Bone marrow stromal cells (BMSCs) isolated from AMBN mutant mice displayed defects in proliferation and differentiation potential as well as cytoskeleton organization. Osteogenesis‐related growth factors, such as insulin‐like growth factor 1 (IGF1) and BMP7, were also significantly (46% to 73%) reduced in AMBN‐deficient BMSCs. Addition of exogenous AMBN restored cytoskeleton structures in AMBN mutant BMSCs and resulted in a dramatic 400% to 600% increase in BMP2, BMP7, and Col1A expression. Block of RhoA diminished the effect of AMBN on osteogenic growth factor and matrix protein gene expression. Addition of exogenous BMP7 and IGF1 rescued the proliferation and differentiation potential of AMBN‐deficient BMSCs. Confirming the effects of AMBN on long bone growth, back‐crossing of mutant mice with full‐length AMBN overexpressors resulted in a complete rescue of AMBNΔ5–6 bone defects. Together, these data indicate that AMBN affects extracellular matrix production and cell adhesion properties in the long bone growth plate, resulting in altered cytoskeletal dynamics, increased osteogenesis‐related gene expression, as well as osteoblast and chondrocyte proliferation. We propose that AMBN facilitates rapid long bone growth and an important growth spurt during the skeletogenesis of adolescent tooth‐bearing vertebrates. © 2016 American Society for Bone and Mineral Research.</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1002/jbmr.2788</identifier><identifier>PMID: 26766111</identifier><identifier>CODEN: JBMREJ</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>AMELOBLASTIN ; Animals ; BMP7 ; Bone Density - physiology ; BONE DEVELOPMENT ; Bone Morphogenetic Protein 7 - genetics ; Bone Morphogenetic Protein 7 - metabolism ; Dental Enamel Proteins - genetics ; Dental Enamel Proteins - metabolism ; Extracellular Matrix Proteins - genetics ; Extracellular Matrix Proteins - metabolism ; Femur - growth &amp; development ; IGF1 ; Insulin-Like Growth Factor I - genetics ; Insulin-Like Growth Factor I - metabolism ; MESENCHYMAL CELLS ; Mice ; Mice, Knockout ; Osteogenesis - physiology</subject><ispartof>Journal of bone and mineral research, 2016-06, Vol.31 (6), p.1235-1246</ispartof><rights>2016 American Society for Bone and Mineral Research</rights><rights>2016 American Society for Bone and Mineral Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4878-879778b44a28af0dcdbdb9cc89840320ee326fb6f79a9739374c4bcb746e06fc3</citedby><cites>FETCH-LOGICAL-c4878-879778b44a28af0dcdbdb9cc89840320ee326fb6f79a9739374c4bcb746e06fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbmr.2788$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbmr.2788$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26766111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Xuanyu</creatorcontrib><creatorcontrib>Fukumoto, Satoshi</creatorcontrib><creatorcontrib>Yamada, Yoshihiko</creatorcontrib><creatorcontrib>Evans, Carla A</creatorcontrib><creatorcontrib>Diekwisch, Thomas GH</creatorcontrib><creatorcontrib>Luan, Xianghong</creatorcontrib><title>Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone Growth and Mineralization</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>ABSTRACT Matrix molecules such as the enamel‐related calcium‐binding phosphoprotein ameloblastin (AMBN) are expressed in multiple tissues, including teeth, bones, and cartilage. Here we have asked whether AMBN is of functional importance for timely long bone development and, if so, how it exerts its function related to osteogenesis. Adolescent AMBN‐deficient mice (AMBNΔ5–6) suffered from a 33% to 38% reduction in femur length and an 8.4% shorter trunk spinal column when compared with WT controls, whereas there was no difference between adult animals. On a cellular level, AMBN truncation resulted in a shortened growth plate and a 41% to 49% reduction in the number of proliferating tibia chondrocytes and osteoblasts. Bone marrow stromal cells (BMSCs) isolated from AMBN mutant mice displayed defects in proliferation and differentiation potential as well as cytoskeleton organization. Osteogenesis‐related growth factors, such as insulin‐like growth factor 1 (IGF1) and BMP7, were also significantly (46% to 73%) reduced in AMBN‐deficient BMSCs. Addition of exogenous AMBN restored cytoskeleton structures in AMBN mutant BMSCs and resulted in a dramatic 400% to 600% increase in BMP2, BMP7, and Col1A expression. Block of RhoA diminished the effect of AMBN on osteogenic growth factor and matrix protein gene expression. Addition of exogenous BMP7 and IGF1 rescued the proliferation and differentiation potential of AMBN‐deficient BMSCs. Confirming the effects of AMBN on long bone growth, back‐crossing of mutant mice with full‐length AMBN overexpressors resulted in a complete rescue of AMBNΔ5–6 bone defects. Together, these data indicate that AMBN affects extracellular matrix production and cell adhesion properties in the long bone growth plate, resulting in altered cytoskeletal dynamics, increased osteogenesis‐related gene expression, as well as osteoblast and chondrocyte proliferation. We propose that AMBN facilitates rapid long bone growth and an important growth spurt during the skeletogenesis of adolescent tooth‐bearing vertebrates. © 2016 American Society for Bone and Mineral Research.</description><subject>AMELOBLASTIN</subject><subject>Animals</subject><subject>BMP7</subject><subject>Bone Density - physiology</subject><subject>BONE DEVELOPMENT</subject><subject>Bone Morphogenetic Protein 7 - genetics</subject><subject>Bone Morphogenetic Protein 7 - metabolism</subject><subject>Dental Enamel Proteins - genetics</subject><subject>Dental Enamel Proteins - metabolism</subject><subject>Extracellular Matrix Proteins - genetics</subject><subject>Extracellular Matrix Proteins - metabolism</subject><subject>Femur - growth &amp; development</subject><subject>IGF1</subject><subject>Insulin-Like Growth Factor I - genetics</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>MESENCHYMAL CELLS</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Osteogenesis - physiology</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UFLwzAUB_AgipvTg19ACl4UrEuaLEmPc8ypbCiiFy8lSVPtaBNNWrb56W236UEQL-9dfu8Pjz8AxwheIgij_lyW7jJinO-ALhpEOCSUo13QhZyTEBKMOuDA-zmEkA4o3QediDJKEUJd8DIsdWFlIXyVm4tAmGC8rJxQuijqQrhgJiqXL4MHZyvdgmGWaVX5YGrNa3BljQ4mzi6qt-YyDWa50U4U-aeocmsOwV4mCq-PtrsHnq_HT6ObcHo_uR0Np6EinPGQs5gxLgkRERcZTFUqUxkrxWNOII6g1jiimaQZi0XMcIwZUUQqyQjVkGYK98DZJvfd2Y9a-yopc98-IIy2tU8Qh5zhZuL_KYtxjCBisKGnv-jc1s40j6wVopxT1KjzjVLOeu90lry7vBRulSCYtN0kbTdJ201jT7aJtSx1-iO_y2hAfwMWeaFXfycld1ezx3XkF7Yxl8c</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Lu, Xuanyu</creator><creator>Fukumoto, Satoshi</creator><creator>Yamada, Yoshihiko</creator><creator>Evans, Carla A</creator><creator>Diekwisch, Thomas GH</creator><creator>Luan, Xianghong</creator><general>Wiley Subscription Services, Inc</general><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>7TS</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201606</creationdate><title>Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone Growth and Mineralization</title><author>Lu, Xuanyu ; Fukumoto, Satoshi ; Yamada, Yoshihiko ; Evans, Carla A ; Diekwisch, Thomas GH ; Luan, Xianghong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4878-879778b44a28af0dcdbdb9cc89840320ee326fb6f79a9739374c4bcb746e06fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>AMELOBLASTIN</topic><topic>Animals</topic><topic>BMP7</topic><topic>Bone Density - physiology</topic><topic>BONE DEVELOPMENT</topic><topic>Bone Morphogenetic Protein 7 - genetics</topic><topic>Bone Morphogenetic Protein 7 - metabolism</topic><topic>Dental Enamel Proteins - genetics</topic><topic>Dental Enamel Proteins - metabolism</topic><topic>Extracellular Matrix Proteins - genetics</topic><topic>Extracellular Matrix Proteins - metabolism</topic><topic>Femur - growth &amp; development</topic><topic>IGF1</topic><topic>Insulin-Like Growth Factor I - genetics</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>MESENCHYMAL CELLS</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Osteogenesis - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Xuanyu</creatorcontrib><creatorcontrib>Fukumoto, Satoshi</creatorcontrib><creatorcontrib>Yamada, Yoshihiko</creatorcontrib><creatorcontrib>Evans, Carla A</creatorcontrib><creatorcontrib>Diekwisch, Thomas GH</creatorcontrib><creatorcontrib>Luan, Xianghong</creatorcontrib><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>Physical Education Index</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Xuanyu</au><au>Fukumoto, Satoshi</au><au>Yamada, Yoshihiko</au><au>Evans, Carla A</au><au>Diekwisch, Thomas GH</au><au>Luan, Xianghong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone Growth and Mineralization</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2016-06</date><risdate>2016</risdate><volume>31</volume><issue>6</issue><spage>1235</spage><epage>1246</epage><pages>1235-1246</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>ABSTRACT Matrix molecules such as the enamel‐related calcium‐binding phosphoprotein ameloblastin (AMBN) are expressed in multiple tissues, including teeth, bones, and cartilage. Here we have asked whether AMBN is of functional importance for timely long bone development and, if so, how it exerts its function related to osteogenesis. Adolescent AMBN‐deficient mice (AMBNΔ5–6) suffered from a 33% to 38% reduction in femur length and an 8.4% shorter trunk spinal column when compared with WT controls, whereas there was no difference between adult animals. On a cellular level, AMBN truncation resulted in a shortened growth plate and a 41% to 49% reduction in the number of proliferating tibia chondrocytes and osteoblasts. Bone marrow stromal cells (BMSCs) isolated from AMBN mutant mice displayed defects in proliferation and differentiation potential as well as cytoskeleton organization. Osteogenesis‐related growth factors, such as insulin‐like growth factor 1 (IGF1) and BMP7, were also significantly (46% to 73%) reduced in AMBN‐deficient BMSCs. Addition of exogenous AMBN restored cytoskeleton structures in AMBN mutant BMSCs and resulted in a dramatic 400% to 600% increase in BMP2, BMP7, and Col1A expression. Block of RhoA diminished the effect of AMBN on osteogenic growth factor and matrix protein gene expression. Addition of exogenous BMP7 and IGF1 rescued the proliferation and differentiation potential of AMBN‐deficient BMSCs. Confirming the effects of AMBN on long bone growth, back‐crossing of mutant mice with full‐length AMBN overexpressors resulted in a complete rescue of AMBNΔ5–6 bone defects. Together, these data indicate that AMBN affects extracellular matrix production and cell adhesion properties in the long bone growth plate, resulting in altered cytoskeletal dynamics, increased osteogenesis‐related gene expression, as well as osteoblast and chondrocyte proliferation. We propose that AMBN facilitates rapid long bone growth and an important growth spurt during the skeletogenesis of adolescent tooth‐bearing vertebrates. © 2016 American Society for Bone and Mineral Research.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>26766111</pmid><doi>10.1002/jbmr.2788</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0884-0431
ispartof Journal of bone and mineral research, 2016-06, Vol.31 (6), p.1235-1246
issn 0884-0431
1523-4681
language eng
recordid cdi_proquest_miscellaneous_1808731803
source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects AMELOBLASTIN
Animals
BMP7
Bone Density - physiology
BONE DEVELOPMENT
Bone Morphogenetic Protein 7 - genetics
Bone Morphogenetic Protein 7 - metabolism
Dental Enamel Proteins - genetics
Dental Enamel Proteins - metabolism
Extracellular Matrix Proteins - genetics
Extracellular Matrix Proteins - metabolism
Femur - growth & development
IGF1
Insulin-Like Growth Factor I - genetics
Insulin-Like Growth Factor I - metabolism
MESENCHYMAL CELLS
Mice
Mice, Knockout
Osteogenesis - physiology
title Ameloblastin, an Extracellular Matrix Protein, Affects Long Bone 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=2025-02-05T04%3A34%3A16IST&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=Ameloblastin,%20an%20Extracellular%20Matrix%20Protein,%20Affects%20Long%20Bone%20Growth%20and%20Mineralization&rft.jtitle=Journal%20of%20bone%20and%20mineral%20research&rft.au=Lu,%20Xuanyu&rft.date=2016-06&rft.volume=31&rft.issue=6&rft.spage=1235&rft.epage=1246&rft.pages=1235-1246&rft.issn=0884-0431&rft.eissn=1523-4681&rft.coden=JBMREJ&rft_id=info:doi/10.1002/jbmr.2788&rft_dat=%3Cproquest_cross%3E4074843901%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=1793168861&rft_id=info:pmid/26766111&rfr_iscdi=true