Literature DB >> 26927967

MEPE Localization in the Craniofacial Complex and Function in Tooth Dentin Formation.

Angela Gullard1,2, Jelica Gluhak-Heinrich3, Silvana Papagerakis4, Philip Sohn1, Aaron Unterbrink5, Shuo Chen6, Mary MacDougall1.   

Abstract

Matrix extracellular phosphoglycoprotein (MEPE) is an extracellular matrix protein found in dental and skeletal tissues. Although information regarding the role of MEPE in bone and disorders of phosphate metabolism is emerging, the role of MEPE in dental tissues remains unclear. We performed RNA in situ hybridization and immunohistochemistry analyses to delineate the expression pattern of MEPE during embryonic and postnatal development in craniofacial mineralizing tissues. Mepe RNA expression was seen within teeth from cap through root formation in association with odontoblasts and cellular cementoblasts. More intense expression was seen in the alveolar bone within the osteoblasts and osteocytes. MEPE immunohistochemistry showed biphasic dentin staining in incisors and more intense staining in alveolar bone matrix and in forming cartilage. Analysis of Mepe null mouse molars showed overall mineralized tooth volume and density of enamel and dentin comparable with that of wild-type samples. However, Mepe(-/-) molars exhibited increased thickness of predentin, dentin, and enamel over controls and decreased gene expression of Enam, Bsp, Dmp1, Dspp, and Opnby RT-PCR. In vitro Mepe overexpression in odontoblasts led to significant reductions in Dspp reporter activity. These data suggest MEPE may be instrumental in craniofacial and dental matrix maturation, potentially functioning in the maintenance of non-mineralized matrix.
© 2016 The Histochemical Society.

Entities:  

Keywords:  MEPE; alveolar bone; dentin; immunohistochemistry; in situ hybridization; matrix mineralization

Mesh:

Substances:

Year:  2016        PMID: 26927967      PMCID: PMC4817730          DOI: 10.1369/0022155416635569

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  34 in total

1.  MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21.

Authors:  Mary MacDougall; Darrin Simmons; Ting Ting Gu; Juan Dong
Journal:  Connect Tissue Res       Date:  2002       Impact factor: 3.417

2.  Mepe, the gene encoding a tumor-secreted protein in oncogenic hypophosphatemic osteomalacia, is expressed in bone.

Authors:  L Argiro; M Desbarats; F H Glorieux; B Ecarot
Journal:  Genomics       Date:  2001-06-15       Impact factor: 5.736

3.  Targeted disruption of the osteoblast/osteocyte factor 45 gene (OF45) results in increased bone formation and bone mass.

Authors:  Lori C Gowen; Donna N Petersen; Amy L Mansolf; Hong Qi; Jeffrey L Stock; George T Tkalcevic; Hollis A Simmons; David T Crawford; Kristen L Chidsey-Frink; Hua Zhu Ke; John D McNeish; Thomas A Brown
Journal:  J Biol Chem       Date:  2002-11-05       Impact factor: 5.157

4.  Identification of osteoblast/osteocyte factor 45 (OF45), a bone-specific cDNA encoding an RGD-containing protein that is highly expressed in osteoblasts and osteocytes.

Authors:  D N Petersen; G T Tkalcevic; A L Mansolf; R Rivera-Gonzalez; T A Brown
Journal:  J Biol Chem       Date:  2000-11-17       Impact factor: 5.157

5.  MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia.

Authors:  P S Rowe; P A de Zoysa; R Dong; H R Wang; K E White; M J Econs; C L Oudet
Journal:  Genomics       Date:  2000-07-01       Impact factor: 5.736

6.  MEPE has the properties of an osteoblastic phosphatonin and minhibin.

Authors:  P S N Rowe; Y Kumagai; G Gutierrez; I R Garrett; R Blacher; D Rosen; J Cundy; S Navvab; D Chen; M K Drezner; L D Quarles; G R Mundy
Journal:  Bone       Date:  2004-02       Impact factor: 4.398

7.  Dentonin, a fragment of MEPE, enhanced dental pulp stem cell proliferation.

Authors:  H Liu; W Li; C Gao; Y Kumagai; R W Blacher; P K DenBesten
Journal:  J Dent Res       Date:  2004-06       Impact factor: 6.116

8.  Six genes expressed in bones and teeth encode the current members of the SIBLING family of proteins.

Authors:  Larry W Fisher; Neal S Fedarko
Journal:  Connect Tissue Res       Date:  2003       Impact factor: 3.417

Review 9.  Dental structural diseases mapping to human chromosome 4q21.

Authors:  Mary MacDougall
Journal:  Connect Tissue Res       Date:  2003       Impact factor: 3.417

10.  MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia.

Authors:  Benjamin Salmon; Claire Bardet; Mayssam Khaddam; Jiar Naji; Benjamin R Coyac; Brigitte Baroukh; Franck Letourneur; Julie Lesieur; Franck Decup; Dominique Le Denmat; Antonino Nicoletti; Anne Poliard; Peter S Rowe; Eric Huet; Sibylle Opsahl Vital; Agnès Linglart; Marc D McKee; Catherine Chaussain
Journal:  PLoS One       Date:  2013-02-22       Impact factor: 3.240

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  3 in total

1.  Photobiomodulation therapy does not depend on the differentiation of dental pulp cells to enhance functional activity associated with angiogenesis and mineralization.

Authors:  Daniela Thomazatti Chimello-Sousa; Geovane Praxedes Lavez; Roger Rodrigo Fernandes; Milla Sprone Tavares; Adalberto Luiz Rosa; Selma Siessere; Simone Cecílio Hallak Regalo; Karina Fittipaldi Bombonato-Prado
Journal:  Lasers Med Sci       Date:  2021-08-10       Impact factor: 3.161

2.  Overlapping functions of bone sialoprotein and pyrophosphate regulators in directing cementogenesis.

Authors:  M Ao; M B Chavez; E Y Chu; K C Hemstreet; Y Yin; M C Yadav; J L Millán; L W Fisher; H A Goldberg; M J Somerman; B L Foster
Journal:  Bone       Date:  2017-09-01       Impact factor: 4.398

3.  The Genes Involved in Dentinogenesis.

Authors:  Shuang Chen; Han Xie; Shouliang Zhao; Shuai Wang; Xiaoling Wei; Shangfeng Liu
Journal:  Organogenesis       Date:  2022-01-13       Impact factor: 2.500

  3 in total

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