Novel role of zonula occludens-1: A tight junction protein closely associated with the odontoblast differentiation of human dental pulp cells

被引:11
|
作者
Xu, Jue [1 ]
Shao, Meiying [2 ]
Pan, Hongying [3 ]
Wang, Huning [3 ]
Cheng, Li [1 ]
Yang, Hui [4 ]
Hu, Tao [1 ,3 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Dept Prevent Dent, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
[2] Sichuan Univ, Coll Life Sci, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
[3] Sichuan Univ, West China Hosp Stomatol, Dept Operat Dent & Endodont, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
[4] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
cell-cell junctions; human dental pulp cells; odontoblast differentiation; ZO-1; LYSOPHOSPHATIDIC ACID; RHO; ZO-1; ORGANIZATION; COMPLEXES; MINERALIZATION; LOCALIZATION; AMELOBLASTS; ACTIVATION; ADHERENS;
D O I
10.1002/cbin.10617
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zonula occludens-1 (ZO-1), a tight junction protein, contributes to the maintenance of the polarity of odontoblasts and junctional complex formation in odontoblast layer during tooth development. However, expression and possible role of ZO-1 in human dental pulp cells (hDPCs) during repair process remains unknown. Here, we investigated the expression of ZO-1 in hDPCs and the relationship with odontoblast differentiation. We found the processes of two adjacent cells were fused and formed junction-like structure using scanning electron microscopy. Fluorescence immunoassay and Western blot confirmed ZO-1 expression in hDPCs. Especially, ZO-1 was high expressed at the cell-cell junction sites. More interestingly, ZO-1 accumulated at the leading edge of lamellipodia in migrating cells when a scratch assay was performed. Furthermore, ZO-1 gradual increased during odontoblast differentiation and ZO-1 silencing greatly inhibited the differentiation. ZO-1 binds directly to actin filaments and RhoA/ROCK signaling mainly regulates cell cytoskeleton, thus RhoA/ROCK might play a role in regulating ZO-1. Lysophosphatidic acid (LPA) and Y-27632 were used to activate and inhibit RhoA/ROCK signaling, respectively, with or without mineralizing medium. In normal cultured hDPCs, RhoA activation increased ZO-1 expression and especially in intercellular contacts, whereas ROCK inhibition attenuated the effects induced by LPA. However, expression of ZO-1 was upregulated by Y-27632 but not significantly affected by LPA after odontoblast differentiation. Hence, ZO-1 highly expresses in cell-cell junctions and is related to odontoblast differentiation, which may contribute to dental pulp repair or even the formation of an odontoblast layer. RhoA/ROCK signaling is involved in the regulation of ZO-1.
引用
收藏
页码:787 / 795
页数:9
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