4.6 Article

Nerve Growth Factor Promotes Differentiation of Odontoblast-Like Cells

期刊

JOURNAL OF CELLULAR BIOCHEMISTRY
卷 106, 期 4, 页码 539-545

出版社

WILEY-LISS
DOI: 10.1002/jcb.22006

关键词

ODONTOBLAST; NERVE GROWTH FACTOR; TM14; MINERALIZATION

资金

  1. Japan Society for the Promotion of Science
  2. Ministry of Education, Vulture, Spoils, Science and 'Fechnology of Japan [18300159]
  3. Grants-in-Aid for Scientific Research [18300159] Funding Source: KAKEN

向作者/读者索取更多资源

Contemporary strategies in tooth repair markedly rely on the newest findings on the cellular and biological components of dental development. Among several identified bioactive molecules, neurotrophins were recently proposed to affect tooth germ cell proliferation, differentiation, and cell-extracellular matrix interactions. The present study attempted to explore the effect of nerve growth factor (NGF) on a spontaneously immortalized dental papilla mesenchymal cell line. NGF induced differentiation of odontoblast-lineage cells with subsequent biomineralization in vitro. Here we showed that normalized transcript levels of tissue-specific markers such as DSPP and DMP I were elevated significantly, indicating cell differentiation and maturation processes. We performed innovative gene expression analysis or TM14, a matricellular protein and novel member of the fibulin family. TM14 expression followed a pattern similar to that of DMP 1, which suggests its important role in cell-matrix and intercellular interactions during dentin calcification. Alkaline phosphatase enzyme assay confirmed the extracellular matrix calcifications in NGF-supplemented groups. Thus, NGF was characterized as a potent promoter of mineralization during dentin formation. For the first time, we included TM14 in odontoblast genotype analysis and proved that NGF also promotes in vitro odontoblast differentiation. Collectively, these results highlight the importance of NGF during tooth morphogenesis, as well as urge the elaboration of complex epithelial-mesenchymal tissue cultures, where further elucidation of the signaling factor network could be completed. J. Cell. Biochem. 106: 539-545, 2009. (C) 2009 Wiley-Liss, Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据