Angiogenic microRNA-210 is present in cells surrounding osteonecrosis

被引:54
作者
Yamasaki, Keiichiro [1 ]
Nakasa, Tomoyuki [1 ]
Miyaki, Shigeru [1 ]
Yamasaki, Takuma [1 ]
Yasunaga, Yuji [1 ]
Ochi, Mitsuo [1 ]
机构
[1] Hiroshima Univ, Dept Orthopaed Surg, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348551, Japan
关键词
microRNA-210; osteonecrosis; angiogenesis; femoral head; GENE-EXPRESSION; FEMORAL-HEAD; AVASCULAR NECROSIS; HYPOXIA; DISEASE; GROWTH; IDENTIFICATION; INDUCTION; MECHANISM; SURVIVAL;
D O I
10.1002/jor.22079
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
A role of microRNAs (miRNAs), which are similar to 22-nucleotide non-coding RNAs, has recently been recognized in human diseases. The objective of this study was to identify the expression pattern of miRNA (miR)-210, known to be associated with angiogenesis, in bone from patients with osteonecrosis (ON) of the femoral head. The expression of miR-210 in bone from 10 patients with osteoarthritis (OA) of the hip and ten with ON was analyzed by quantitative reverse transcription-polymerase chain reaction (RT-PCR) and by in situ hybridization. In addition, immunohistochemical staining for von Willebrand factor (vWF) and vascular endothelial growth factor (VEGF) was performed to identify the miR-210 expressing cells. We found that in ON samples, the expression of mature, primary miR-210, VEGF, matrix metalloproteinase (MMP)-2, and MMP-7 was significantly higher than that of OA samples. Section in situ hybridization of mature miR-210 revealed that mature miR-210 is expressed around the necrotic area. vWF and VEGF were also strongly expressed in the miR-210 expressing cells. This study shows that miR-210 is intensely expressed in ON, and might play a role in ON pathogenesis. The present study provides a solid basis for further functional analyses of miRNAs in ON. (C) 2012 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 30:12631270, 2012
引用
收藏
页码:1263 / 1270
页数:8
相关论文
共 62 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   SKELETAL MANIFESTATIONS AND TREATMENT OF GAUCHERS DISEASE - REVIEW OF 20 CASES [J].
AMSTUTZ, HC ;
CAREY, EJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1966, A 48 (04) :670-&
[3]  
ARLET J, 1992, CLIN ORTHOP RELAT R, P12
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   hsa-miR-210 is induced by hypoxia and is an independent prognostic factor in breast cancer [J].
Camps, Carme ;
Buffa, Francesca M. ;
Colella, Stefano ;
Moore, John ;
Sotiriou, Christos ;
Sheldon, Helen ;
Harris, Adrian L. ;
Gleadle, Jonathan M. ;
Ragoussis, Jiannis .
CLINICAL CANCER RESEARCH, 2008, 14 (05) :1340-1348
[6]  
Casey B H, 1972, J Bone Joint Surg Br, V54, P607
[7]  
CHANDLER F A, 1948, J Int Coll Surg, V11, P34
[8]   In-vitro effects of dexamethasone on cellular proliferation, apoptosis, and Na+-K+-ATPase activity of bovine corneal endothelial cells [J].
Chen, Wei-Li ;
Lin, Chung-Tien ;
Yao, Chung-Chen ;
Huang, Yu-Hua ;
Chou, Yu-Bin ;
Yin, Hsiang-Shu ;
Hu, Fung-Rong .
OCULAR IMMUNOLOGY AND INFLAMMATION, 2006, 14 (04) :215-223
[9]   Regulation of angiogenesis through a microRNA (miR-130a) that down-regulates antiangiogenic homeobox genes GAX and HOXA5 [J].
Chen, Yun ;
Gorski, David H. .
BLOOD, 2008, 111 (03) :1217-1226
[10]   MicroRNA Regulation of DNA Repair Gene Expression in Hypoxic Stress [J].
Crosby, Meredith E. ;
Kulshreshtha, Ritu ;
Ivan, Mircea ;
Glazer, Peter M. .
CANCER RESEARCH, 2009, 69 (03) :1221-1229