Cyclic stretch and compression forces alter microRNA-29 expression of human periodontal ligament cells

被引:60
作者
Chen, Yinghua [1 ]
Mohammed, Arshad [1 ]
Oubaidin, Maysaa [1 ]
Evans, Carla A. [1 ]
Zhou, Xiaofeng [2 ,3 ]
Luan, Xianghong [4 ]
Diekwisch, Thomas G. H. [4 ]
Atsawasuwan, Phimon [1 ]
机构
[1] Univ Illinois, Coll Dent, Dept Orthodont, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Dent, Dept Periodont, Chicago, IL USA
[3] Univ Illinois, Ctr Mol Biol Oral Dis, Chicago, IL USA
[4] Univ Illinois, Coll Dent, Dept Oral Biol, Chicago, IL USA
关键词
MicroRNA; Periodontal ligament; Extracellular matrix; Cyclic stretch; Compression; EXTRACELLULAR-MATRIX; TOOTH MOVEMENT; OSTEOGENIC DIFFERENTIATION; STEM-CELLS; TISSUE; COLLAGEN; STRESS; FIBROBLASTS; SUPPRESSION; ACTIVATION;
D O I
10.1016/j.gene.2015.03.055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNAs (miRs) play an important role in the development and remodeling of tissues through the regulation of large cohorts of extracellular matrix (ECM) genes. The purpose of the present study was to determine the response of miR-29 family expression to loading forces and their effects on ECM gene expression in periodontal ligament cells, the key effector cell population during orthodontic tooth movement. In a comparison between miRs from human periodontal ligament cells (PDLCs) and alveolar bone cells (ABCs) from healthy human subjects, the ABC cohort of miRs was substantially greater than the corresponding PDLC cohort. Cyclic mechanical stretch forces at 12% deformation at 0.1 Hz for 24 h decreased expression of miR-29 family member miRs about 0.5 fold while 2 g/cm(2) compression force for 24 h increased miR-29 family member expression in PDLCs 1.8-4 folds. Cyclic stretch up-regulated major ECM genes in PDLCs, such as COL1A1,COL3A1 and COL5A1, while the compression force resulted in a down-regulation of these ECM genes. Direct interactions of miR-29 and Col1a1, Col3a1 and Col5a1 were confirmed using a dual luciferase reporter gene assay. In addition, transient transfection of a miR-29b mimic in mouse PDLCs down-regulated Col1a1, Col3a1 and Col5a1 while the transfection of miR-29b inhibitor up-regulated these genes compared to control transfection indicating that these target ECM genes directly responded to the altered level of miR-29b. These results provided a possible explanation for the effects of the miR-29 family on loaded PDLCS and their roles in extracellular matrix gene expression. Published by Elsevier B.V.
引用
收藏
页码:13 / 17
页数:5
相关论文
共 32 条
[1]   Diversifying microRNA sequence and function [J].
Ameres, Stefan L. ;
Zamore, Phillip D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2013, 14 (08) :475-488
[2]   Expression and Function of Enamel-related Gene Products in Calvarial Development [J].
Atsawasuwan, P. ;
Lu, X. ;
Ito, Y. ;
Chen, Y. ;
Gopinathan, G. ;
Evans, C. A. ;
Kulkarni, A. B. ;
Gibson, C. W. ;
Luan, X. ;
Diekwisch, T. G. H. .
JOURNAL OF DENTAL RESEARCH, 2013, 92 (07) :622-628
[3]   The Noncoding RNA Revolution-Trashing Old Rules to Forge New Ones [J].
Cech, Thomas R. ;
Steitz, Joan A. .
CELL, 2014, 157 (01) :77-94
[4]  
Dangaria SJ, 2011, TISSUE ENG PT A, V17, P279, DOI 10.1089/ten.TEA.2010.0264
[5]   Successful Periodontal Ligament Regeneration by Periodontal Progenitor Preseeding on Natural Tooth Root Surfaces [J].
Dangaria, Smit Jayant ;
Ito, Yoshihiro ;
Luan, Xianghong ;
Diekwisch, Thomas G. H. .
STEM CELLS AND DEVELOPMENT, 2011, 20 (10) :1659-1668
[6]   Temporal and spatial mRNA expression of bone sialoprotein and type I collagen during rodent tooth movement [J].
Domon, S ;
Shimokawa, H ;
Yamaguchi, S ;
Soma, K .
EUROPEAN JOURNAL OF ORTHODONTICS, 2001, 23 (04) :339-348
[7]   miR-146a Induces Differentiation of Periodontal Ligament Cells [J].
Hung, P. -S. ;
Chen, F. -C. ;
Kuang, S. -H. ;
Kao, S. -Y. ;
Lin, S. -C. ;
Chang, K. -W. .
JOURNAL OF DENTAL RESEARCH, 2010, 89 (03) :252-257
[8]  
Iwasaki LR., 2006, Am J Orthod Dentofacial Orthop, V130, pe691
[9]  
Jin Yi, 2013, Methods Mol Biol, V936, P117
[10]   VEGF and M-CSF levels in periodontal tissue during tooth movement [J].
Kaku, Masato ;
Motokawa, Masahide ;
Tohma, Yuiko ;
Tsuka, Natsumi ;
Koseki, Hiroyuki ;
Sunaganwa, Hiroko ;
Hernandes, Rene Arturo Marquez ;
Ohtani, Junji ;
Fujita, Tadashi ;
Kawata, Toshitsugu ;
Tanne, Kazuo .
BIOMEDICAL RESEARCH-TOKYO, 2008, 29 (04) :181-187