AKT from dental epithelium to papilla promotes odontoblast differentiation

被引:1
|
作者
Wang, Jiangyi [1 ,2 ]
Lin, Xiaoyu [1 ,2 ]
Shen, Zongshan [1 ,2 ]
Li, Guoqing [1 ,2 ]
Hu, Lei [1 ,2 ,3 ]
Li, Qiong [1 ,2 ]
Li, Yang [1 ,2 ]
Wang, Jinsong [4 ]
Zhang, Chunmei [1 ,2 ]
Wang, Songlin [1 ,2 ,4 ,5 ,7 ]
Wu, Xiaoshan [5 ,6 ]
机构
[1] Capital Med Univ, Beijing Key Lab Tooth Regenerat & Funct Reconstruc, Beijing Lab Oral Hlth, Beijing 100050, Peoples R China
[2] Capital Med Univ, Beijing Stomatol Hosp, Beijing 100050, Peoples R China
[3] Capital Med Univ, Sch Stomatol, Dept Prosthodont, Beijing 100050, Peoples R China
[4] Capital Med Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Beijing 100069, Peoples R China
[5] Cent South Univ, Academician Workstat Oral Maxillofacial Regenerat, Changsha 410008, Peoples R China
[6] Cent South Univ, Xiangya Hosp, Dept Oral & Maxillofacial Surg, Xiangya Rd 87, Changsha 410008, Peoples R China
[7] Capital Med Univ, Beijing Stomatol Hosp, Beijing Key Lab Tooth Regenerat & Funct Reconstruc, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
Tooth; Development; Dental papilla; Cell interaction; Cell differentiation; Coculture; STEM-CELLS; EXPRESSION; MORPHOGENESIS; SUPPRESSES; PI3K;
D O I
10.1016/j.diff.2023.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial-mesenchymal interactions occur during tooth development. The dental epithelium (DE) is regarded as the signal center that regulates tooth morphology. However, the mechanism by which DE regulates the differentiation of mesenchyme-derived dental papilla (DP) into odontoblasts remains unclear. Using miniature pigs as a model, we analyzed the expression profiles of the DE and DP during odontoblast differentiation using highthroughput RNA sequencing. The phosphatidylinositol-3-kinase (PI3K)/AKT pathway is one of the most enriched pathways in both DE and DP. The PI3K/AKT pathway was first activated in the inner enamel epithelium but not in the DP on embryonic day 50. This pathway was then activated in the odontoblast layer on embryonic day 60. We showed that AKT activation promoted odontoblast differentiation of DP cells. We further demonstrated that activation of PI3K/AKT signaling in the DE effectively increased the expression levels of AKT and dentin sialophosphoprotein in DP cells. Additionally, we found that DE cells secreted collagen type IV alpha 6 chain (COL4A6) downstream of epithelial AKT signaling to positively regulate mesenchymal AKT levels. Therefore, our data suggest that PI3K/AKT signaling from the DE to the DP promotes odontoblast differentiation via COL4A6 secretion.
引用
收藏
页码:52 / 60
页数:9
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