Alteration of MicroRNA Expression of Human Dental Pulp Cells during Odontogenic Differentiation

被引:53
作者
Gong, Qimei
Wang, Runfu
Jiang, Hongwei
Lin, Zhengmei [1 ]
Ling, Junqi [1 ]
机构
[1] Sun Yat Sen Univ, Guanghua Sch Stomatol, Dept Operat Dent & Endodont, Guangzhou 510055, Guangdong, Peoples R China
关键词
Differentiation; gene ontology; human dental pulp cells; microRNAs; odontoblasts; pathway analysis; ACTIVATED PROTEIN-KINASE; MESENCHYMAL STEM-CELLS; OSTEOGENIC DIFFERENTIATION; MINERALIZATION; COLLAGEN; TISSUES; COL5A1;
D O I
10.1016/j.joen.2012.06.016
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: MicroRNAs (miRNAs) play momentous roles in various biological processes including cell differentiation. However, little is known about the role of miRNAs in human dental pulp cells (hDPCs) during odontogenic differentiation. The aims of this study were to investigate the expression of miRNAs in the primary culture of hDPCs when incubated in odontogenic medium. Methods: The potential characteristics of hDPCs were investigated by miRNA microarray and real-time reverse transcriptase polymerase chain reaction. Bioinformatics (ie, target prediction, Gene Ontology analysis, and Kyoto Encyclopedia of Genes and Genomes mapping tools) were applied for predicting the complementary target genes of miRNAs and their biological functions. Results: A total of 22 miRNAs were differentially expressed in which 12 miRNAs up-regulated and 10 miRNAs down-regulated in differentiated hDPCs compared with the control. The target genes of differential miRNAs were predicted to associate with several biological functions and signaling pathways including the mitogen-activated protein kinase (MAPK) and the Wnt signaling pathway. Conclusions: The differential expression miRNAs may be involved in governing hDPC odontogenic differentiation, thus contributing to the future investigations of regulatory mechanisms in reparative dentin formation and dental pulp regeneration. (J Endod 2012;38:1348-1354)
引用
收藏
页码:1348 / 1354
页数:7
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