4.6 Article

Effects of transforming growth factor-131 on odontoblastic differentiation in dental papilla cells is determined by IPO7 expression level

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2021.01.076

关键词

TGF-131; Importin 7; Mouse dental papilla cells (mDPCs); Mouse dental papilla cell line; P-SMAD2; Odontoblastic differentiation

资金

  1. National Natural Science Foundation of China [81570942]

向作者/读者索取更多资源

TGF-131 plays dual roles in odontoblast differentiation in mouse dental papilla cells, which is determined by IPO7.
Transforming growth factor 131 (TGF-131) is one of the broad-spectrum growth-promoting factors that participate in tooth development. The influence of TGF-131 on the odontoblastic differentiation is still controvercy. Mouse primary dental papilla cells (mDPCs) as well as an immortalized mouse dental papilla cell line (mDPC6Ts) were treated with exogenous TGF-131 during odontoblastic differentiation. RTqPCR, Western blot, alizarin red staining and ALP staining were carried out to investigate the influence of TGF-131 on odontoblastic differentiation. IPO7, important for SMAD complex translocation was also detected in mDPCs and mDPC6Ts in response to TGF-131. After silencing IPO7 by transfection, the translocation process of P-SMAD2 was investigated by nuclear and cytoplasmic extraction as well as coimmunoprecipitation assay. The odontogenic markers, mineralization and IPO7 expression were significantly up-regulated in TGF-131-treated mDPCs while down-regulated in mDPC6Ts. The total level of PSMAD2 was not influenced by IPO7 in mDPCs, however, IPO7 could bind to P-SMAD2 and affect the nuclear-cytoplasm-shuttling of P-SMAD2. Our data demonstrated that TGF-131 plays opposite roles in odontoblast differentiation in mDPCs and immortalized mouse dental papilla cell line (mDPC6Ts), which is determined by IPO7. (c) 2021 Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).

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