Literature DB >> 8894143

Expression of matrix proteins during the development of mineralized tissues.

B Sommer1, M Bickel, W Hofstetter, A Wetterwald.   

Abstract

The specific properties of mineralized tissues are defined by the composition of the fraction of the noncollagenous matrix proteins. Because these proteins play a pivotal role in the processes of cell differentiation and activation and of mineralization, their temporal and spatial expression is tightly regulated. Within this study, the expression of the enamel protein amelogenin and of the bone matrix proteins osteopontin, bone sialoprotein, osteocalcin, and osteonectin was investigated by in situ hybridization. Two models that allow observation of the formation of mineralized tissues were chosen. The development of bone and cartilage was observed on murine metatarsals from 15-day-old embryos up to 1-day-old mice. This time covers the periods of initial bone formation as well as onset of resorption of mineralized cartilage and bone. To study gene expression in the mineralized tissues of the dental organ, enamel, dentin, and cementum, developing molars ranging in age from 16-day-old embryos to 14 days after delivery were chosen. Within this time frame, the molars develop from an immature state to the differentiated organ which erupts through the mandibular bone. In the developing metatarsals, osteopontin and bone sialoprotein mRNAs were detected in osteoblasts and hypertrophic chondrocytes at the onset of mineralization. In the tooth organ, only cementoblasts expressed transcripts encoding the two proteins; odontoblasts and ameloblasts did not express these genes. Osteonectin was expressed by osteoblasts and hypertrophic chondrocytes as well, whereas in the molars it was produced exclusively by odontoblasts. Osteocalcin was expressed specifically by osteoblasts in the developing metatarsals. In tooth, osteocalcin transcripts were detected in odontoblasts. Finally, amelogenin was a specific product of ameloblasts. Thus, a sequential and cell type-restricted expression of matrix proteins takes place during the development of the mineralized tissues. The expression patterns of the transcripts encoding the bone matrix proteins suggest different biological roles depending on the time and site of expression.

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Year:  1996        PMID: 8894143     DOI: 10.1016/s8756-3282(96)00218-9

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  32 in total

1.  Distinctive expression of extracellular matrix molecules at mRNA and protein levels during formation of cellular and acellular cementum in the rat.

Authors:  Y Sasano; Y Maruya; H Sato; J X Zhu; I Takahashi; I Mizoguchi; M Kagayama
Journal:  Histochem J       Date:  2001-02

2.  Osteogenic potential of human periosteum-derived progenitor cells in PLGA scaffold using allogeneic serum.

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Journal:  J Zhejiang Univ Sci B       Date:  2006-10       Impact factor: 3.066

3.  Osteocalcin and matrix GLA protein in developing teleost teeth: identification of sites of mRNA and protein accumulation at single cell resolution.

Authors:  J B Ortiz-Delgado; D C Simes; P Gavaia; C Sarasquete; M L Cancela
Journal:  Histochem Cell Biol       Date:  2005-09-29       Impact factor: 4.304

4.  Alteration of newly induced endochondral bone formation in adult mice without tumour necrosis factor receptor 1.

Authors:  I K Lukić; D Grcević; N Kovacić; V Katavić; S Ivcević; I Kalajzić; A Marusić
Journal:  Clin Exp Immunol       Date:  2005-02       Impact factor: 4.330

5.  In situ hybridization and immunohistochemistry of bone sialoprotein and secreted phosphoprotein 1 (osteopontin) in the developing mouse mandibular condylar cartilage compared with limb bud cartilage.

Authors:  Shunichi Shibata; Kenji Fukada; Shoichi Suzuki; Takuya Ogawa; Yasuo Yamashita
Journal:  J Anat       Date:  2002-03       Impact factor: 2.610

6.  Osteogenic and angiogenic potentials of monocultured and co-cultured human-bone-marrow-derived mesenchymal stem cells and human-umbilical-vein endothelial cells on three-dimensional porous beta-tricalcium phosphate scaffold.

Authors:  Yunqing Kang; Sungwoo Kim; Monica Fahrenholtz; Ali Khademhosseini; Yunzhi Yang
Journal:  Acta Biomater       Date:  2012-08-16       Impact factor: 8.947

7.  Convergent extension movements in growth plate chondrocytes require gpi-anchored cell surface proteins.

Authors:  Molly J Ahrens; Yuwei Li; Hongmei Jiang; Andrew T Dudley
Journal:  Development       Date:  2009-09-17       Impact factor: 6.868

8.  Fate of HERS during tooth root development.

Authors:  Xiaofeng Huang; Pablo Bringas; Harold C Slavkin; Yang Chai
Journal:  Dev Biol       Date:  2009-07-01       Impact factor: 3.582

9.  Responses of bone to titania-hydroxyapatite composite and nacreous implants: a preliminary comparison by in situ hybridization.

Authors:  H Liao; C Brandsten; C Lundmark; T Wurtz; J Li
Journal:  J Mater Sci Mater Med       Date:  1997-12       Impact factor: 3.896

10.  A BAC-bacterial recombination method to generate physically linked multiple gene reporter DNA constructs.

Authors:  Peter Maye; Mary Louise Stover; Yaling Liu; David W Rowe; Shiaochin Gong; Alexander C Lichtler
Journal:  BMC Biotechnol       Date:  2009-03-13       Impact factor: 2.563

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