Mutant GDF5 enhances ameloblast differentiation via accelerated BMP2-induced Smad1/5/8 phosphorylation

• Liu, Jia

• Saito, Kan

• Maruya, Yuriko

• Nakamura, Takashi

• Yamada, Aya

• Fukumoto, Emiko

• Ishikawa, Momoko

• Iwamoto, Tsutomu

• Miyazaki, Kanako

• Yoshizaki, Keigo

• Ge, Lihong

• Fukumoto, Satoshi

抄録

Bone morphogenetic proteins (BMPs) regulate hard tissue formation, including bone and tooth. Growth differentiation factor 5 (GDF5), a known BMP, is expressed in cartilage and regulates chondrogenesis, and mutations have been shown to cause osteoarthritis. Notably, GDF5 is also expressed in periodontal ligament tissue; however, its role during tooth development is unclear. Here, we used cell culture and in vivo analyses to determine the role of GDF5 during tooth development. GDF5 and its associated BMP receptors are expressed at the protein and mRNA levels during postnatal tooth development, particularly at a stage associated with enamel formation. Furthermore, whereas BMP2 was observed to induce evidently the differentiation of enamel-forming ameloblasts, excess GDF5 induce mildly this differentiation. A mouse model harbouring a mutation in GDF5 (W408R) showed enhanced enamel formation in both the incisors and molars, but not in the tooth roots. Overexpression of the W408R GDF5 mutant protein was shown to induce BMP2-mediated mRNA expression of enamel matrix proteins and downstream phosphorylation of Smad1/5/8. These results suggest that mutant GDF5 enhances ameloblast differentiation via accelerated BMP2-signalling.

収録刊行物

• Scientific Reports

  Scientific Reports 6 23670-, 2016-03-31

  Springer Nature

詳細情報

• CRID: 1050282812738701568
• NII論文ID: 120006534957
• ISSN: 20452322
• Web Site: http://repo.lib.tokushima-u.ac.jp/112314
• 本文言語コード: en
• 資料種別: journal article
• データソース種別:
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  • CiNii Articles