共 30 条
MicroRNA-27 promotes the differentiation of odontoblastic cell by targeting APC and activating Wnt/β-catenin signaling
被引:46
作者:
Park, Min-Gyeong
[1
]
Kim, Jae-Sung
[1
]
Park, Sun-Young
[1
]
Lee, Seul Ah
[1
]
Kim, Heung-Joong
[1
]
Kim, Chun Sung
[1
]
Kim, Jin-Soo
[1
]
Chun, Hong Sung
[2
]
Park, Joo-Cheol
[3
,4
]
Kim, Do Kyung
[1
]
机构:
[1] Chosun Univ, Sch Dent, Oral Biol Res Inst, Kwangju 501759, South Korea
[2] Chosun Univ, Dept Biotechnol, Kwangju 501759, South Korea
[3] Seoul Natl Univ, Sch Dent, Dept Oral Histol Dev Biol, Seoul 110749, South Korea
[4] Seoul Natl Univ, Dent Res Inst, Seoul 110749, South Korea
来源:
基金:
新加坡国家研究基金会;
关键词:
miR-27;
Odontoblasts;
Differentiation;
beta-Catenin;
Adenomatous polyposis coli;
BETA-CATENIN;
CANCER;
WNT;
PROLIFERATION;
ADIPOGENESIS;
EXPRESSION;
DENTIN;
MIR-27;
ROLES;
D O I:
10.1016/j.gene.2014.01.045
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
MicroRNAs (miRNAs) play an essential role in regulating cell differentiation either by inhibiting mRNA translation or by inducing its degradation. However, the role of miRNAs in odontoblastic cell differentaion is largely unknown. In the present study, we demonstrate that the expression of miR-27 was significantly increased during MDPC-23 odontoblastic cell differentiation. Furthermore, the up-regulation of miR-27 promotes the differentiation of MDPC-23 odontoblastic cells and accelerates mineralization without cell proliferation. In addition, our results of target gene prediction revealed that the mRNA of adenomatous polyposis coli (APC) associated with Wnt/beta-catenin signaling pathway has miR-27 binding site in the its 3' UTR and is suppressed by miR-27. Subsequentially, the down-regulated APC by miR-27 triggered the activation of Wnt/beta-catenin signaling through accumulation of beta-catenin in the nucleus. Our data suggest that miR-27 promotes MDPC-23 odontoblastic cell differentiation by targeting APC and activating Wnt/beta-catenin signaling. Therefore, miR-27 might be considered a critical candidate as an odontoblastic differentiation molecular target for the development of miRNA based therapeutic agents in the dental medicine. (C) 2014 Elsevier B.V. All rights reserved.
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页码:266 / 272
页数:7
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