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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.
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页码:787 / 795
页数:9
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