A whole-genome transcriptome analysis of articular chondrocytes in secondary osteoarthritis of the hip

被引:24
作者
Aki, Takashi [1 ]
Hashimoto, Ko [1 ]
Ogasawara, Masanori [1 ]
Itoi, Eiji [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Orthopaed Surg, Sendai, Miyagi, Japan
关键词
IGF-BINDING PROTEINS; GENE-EXPRESSION; ACETABULAR DYSPLASIA; EXTRACELLULAR-MATRIX; CPG SITES; IN-VITRO; CARTILAGE; MECHANISMS; BIOLOGY; JAPAN;
D O I
10.1371/journal.pone.0199734
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective To date, exhaustive gene expression analyses of chondrocytes in hip osteoarthritis (OA) have yielded specific gene expression patterns. No study has reported on the exhaustive transcriptome of secondary hip OA based on acetabular dysplasia in a Japanese population, while previous reports have focused on primary or idiopathic hip OA in Caucasian populations. This study aims to search for specific gene expression patterns of secondary hip OA chondrocytes by transcriptome analysis. Design Human articular cartilage was obtained from femoral heads following hemiarthroplasty for femoral neck fracture (N = 8; non-OA) and total hip arthroplasty for secondary hip OA (N = 12). Total RNA was extracted from the articular cartilage and submitted for microarray analysis. The obtained data were used to perform gene expression analysis, GO enrichment analysis and pathway analysis and were compared with data from primary hip OA in Caucasian populations in the literature. Results We identified 888 upregulated (fold change: FC >= 2) and 732 downregulated (FC <= 0.5) genes in hip OA versus non-OA chondrocytes, respectively. Only 10% of upregulated genes were common between the secondary and primary OA. The newly found genes prominently overexpressed in the secondary hip OA chondrocytes were DPT, IGFBP7, and KLF2. Pathway analysis revealed extracellular matrix (ECM)-receptor interaction as an OArelated pathway, which was similar to previous reports in primary hip OA. Conclusions This is the first study to report the genome-wide transcriptome of secondary hip OA chondrocytes and demonstrates new potential OA-related genes. Gene expression patterns were different between secondary and primary hip OA, although the results of pathway and functional analysis were similar.
引用
收藏
页数:17
相关论文
共 46 条
[1]   FoxOs at the crossroads of cellular metabolism, differentiation, and transformation [J].
Accili, D ;
Arden, KC .
CELL, 2004, 117 (04) :421-426
[2]  
Aigner T, 2001, ARTHRITIS RHEUM-US, V44, P2777, DOI 10.1002/1529-0131(200112)44:12<2777::AID-ART465>3.0.CO
[3]  
2-H
[4]   FoxO Transcription Factors Support Oxidative Stress Resistance in Human Chondrocytes [J].
Akasaki, Yukio ;
Alvarez-Garcia, Oscar ;
Saito, Masahiko ;
Carames, Beatriz ;
Iwamoto, Yukihide ;
Lotz, Martin K. .
ARTHRITIS & RHEUMATOLOGY, 2014, 66 (12) :3349-3358
[5]  
[Anonymous], 1971, J JPN ORTHOP ASSOC, V45, P826
[6]  
[Anonymous], OSTEOARTHRITIS CA SA
[7]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[8]   KLF2-induced actin shear fibers control both alignment to flow and JNK signaling in vascular endothelium [J].
Boon, Reinier A. ;
Leyen, Thomas A. ;
Fontijn, Ruud D. ;
Fledderus, Joost O. ;
Baggen, Josefien M. C. ;
Volger, Oscar L. ;
Amerongen, Geerten P. van Nieuw ;
Horrevoets, Anton J. G. .
BLOOD, 2010, 115 (12) :2533-2542
[9]   Molecular mechanisms of osteoarthritis using gene microarrays [J].
Cui, Shuo ;
Zhang, Xinying ;
Hai, Sen ;
Lu, Hong ;
Chen, Yongcai ;
Li, Chao ;
Tong, Pengfei ;
Lu, Fei ;
Yuan, Zhengjiang .
ACTA HISTOCHEMICA, 2015, 117 (01) :62-68
[10]   Cellular and Epigenetic Features of a Young Healthy and a Young Osteoarthritic Cartilage Compared with Aged Control and OA Cartilage [J].
da Silva, Marco A. ;
Yamada, Norikazu ;
Clarke, Nicholas M. P. ;
Roach, Helmtrud I. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2009, 27 (05) :593-601