Literature DB >> 16691493

Ameloblastin fusion protein enhances pulpal healing and dentin formation in porcine teeth.

Y Nakamura1, I Slaby, A Spahr, G Pezeshki, K Matsumoto, S P Lyngstadaas.   

Abstract

Ameloblastin (Ambn, also named "amelin" or "sheathlin") is a protein participating in enamel formation and mesenchymal-ectodermal interaction during early dentin formation in developing teeth. Experiments have demonstrated an association between Ambn expression and healing of acute pulp wounds. The purpose of this study was to investigate if local application of recombinant fusion Ambn (rAmbn) could influence reparative dentin formation in pulpotomized teeth. In this randomized, double-blinded study, pulpotomy was performed in 28 lower central incisors in 17 adult miniature pigs. Following the surgical procedure, the exposed pulp tissue was covered either with rAmbn or with calcium hydroxide. After 2, 4, or 8 weeks, the teeth were extracted and examined by histomorphometry and immunohistochemistry using antibodies against porcine ameloblastin, collagen type I, and dentin sialoprotein (DSP). In rAmbn-treated teeth, a substantial amount of newly formed reparative dentin was observed at the application site, completely bridging the pulpal wound. Dentin formation was also observed in calcium hydroxide-treated teeth; however, the amount of reparative dentin was significantly smaller (P < 0.001) than after rAmbn treatment. Immunohistochemistry confirmed that the new hard tissue formed was similar to dentin. This is the first time a direct link between ameloblastin and dentin formation has been made in vivo. The results suggest potential for rAmbn as a biologically active pulp-dressing agent for enhanced pulpal wound healing and reparative dentin formation after pulpotomy procedures.

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Year:  2006        PMID: 16691493     DOI: 10.1007/s00223-005-0144-2

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  13 in total

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Authors:  Margareth V Tamburstuen; Malcolm L Snead; Janne E Reseland; Michael L Paine; Staale P Lyngstadaas
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4.  Ameloblastin expression and putative autoregulation in mesenchymal cells suggest a role in early bone formation and repair.

Authors:  Margareth V Tamburstuen; Janne E Reseland; Axel Spahr; Steven J Brookes; Gunnar Kvalheim; Ivan Slaby; Malcolm L Snead; S Petter Lyngstadaas
Journal:  Bone       Date:  2010-09-18       Impact factor: 4.398

5.  Critical role of heparin binding domains of ameloblastin for dental epithelium cell adhesion and ameloblastoma proliferation.

Authors:  Akira Sonoda; Tsutomu Iwamoto; Takashi Nakamura; Emiko Fukumoto; Keigo Yoshizaki; Aya Yamada; Makiko Arakaki; Hidemitsu Harada; Kazuaki Nonaka; Seiji Nakamura; Yoshihiko Yamada; Satoshi Fukumoto
Journal:  J Biol Chem       Date:  2009-07-31       Impact factor: 5.157

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7.  Enamel matrix derivative promote primary human pulp cell differentiation and mineralization.

Authors:  Elisabeth Aurstad Riksen; Maria A Landin; Sjur Reppe; Yukio Nakamura; Ståle Petter Lyngstadaas; Janne E Reseland
Journal:  Int J Mol Sci       Date:  2014-05-05       Impact factor: 5.923

8.  Ameloblastin Peptides Modulates the Osteogenic Capacity of Human Mesenchymal Stem Cells.

Authors:  Øystein Stakkestad; Ståle P Lyngstadaas; Jiri Vondrasek; Jan O Gordeladze; Janne Elin Reseland
Journal:  Front Physiol       Date:  2017-02-07       Impact factor: 4.566

9.  Molecular decay of enamel matrix protein genes in turtles and other edentulous amniotes.

Authors:  Robert W Meredith; John Gatesy; Mark S Springer
Journal:  BMC Evol Biol       Date:  2013-01-23       Impact factor: 3.260

10.  Evolutionary analysis of selective constraints identifies ameloblastin (AMBN) as a potential candidate for amelogenesis imperfecta.

Authors:  Frédéric Delsuc; Barbara Gasse; Jean-Yves Sire
Journal:  BMC Evol Biol       Date:  2015-07-30       Impact factor: 3.260

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