Musculoskeletal Research Group, Institute of Cellular Medicine, 4th Floor, Cookson Building, Medical School, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Osteoarthritis Cartilage. 2012 Sep;20(9):1029-38. doi: 10.1016/j.joca.2012.05.006. Epub 2012 May 31.
To define for the first time the transcriptomes of normal and end-stage osteoarthritis (OA) hip cartilage.
RNA was isolated from cartilage within 2h of joint replacement surgery. Gene expression was analyzed using Agilent GeneSpring GX 11 following hybridization to Illumina Human HT-12 V3 microarrays. Real-time reverse-transcription polymerase chain reaction (RT-PCR) was used to validate the expression of six genes identified by microarray as differentially expressed. Gene Set Enrichment Analysis (GSEA) and Ingenuity Pathway Analysis (IPA) were used to investigate enriched functions or canonical pathways amongst differentially expressed genes respectively.
In total we identified 998 differentially expressed genes (fold change ≥ ±1.5, P-value ≤ 0.01) between neck of femur fracture (NOF) (n = 10) and OA hip (n = 9) patient cartilage. These differentially expressed genes were enriched within 71 canonical pathways. A comparison between a comparable knee dataset(20) only identified 229 genes similarly differentially expressed although remarkably 34 canonical pathways overlapped between experiments.
This study is the first to report a comprehensive gene expression analysis of human hip OA cartilage compared to control (NOF) cartilage at the whole-genome level. Our differential gene expression dataset shows excellent correlation with similar defined studies using comparable tissue but reveals discord between hip and knee OA at the individual gene status but with commonality with regards the molecular pathways involved.
首次定义正常和终末期骨关节炎(OA)髋软骨的转录组。
从关节置换手术后 2 小时内的软骨中分离 RNA。使用 Agilent GeneSpring GX 11 对 Illumina Human HT-12 V3 微阵列进行杂交后,分析基因表达。使用实时逆转录聚合酶链反应(RT-PCR)验证微阵列鉴定为差异表达的六个基因的表达。基因集富集分析(GSEA)和 IPA 分别用于研究差异表达基因中富集的功能或经典途径。
总共在股骨颈骨折(NOF)(n = 10)和 OA 髋(n = 9)患者软骨之间鉴定出 998 个差异表达基因(倍数变化≥±1.5,P 值≤0.01)。这些差异表达的基因在 71 个经典途径中富集。与类似的膝关节数据集(20)的比较仅鉴定出 229 个类似差异表达的基因,尽管在实验之间有 34 个经典途径重叠。
这项研究是首次在全基因组水平上比较正常(NOF)软骨与人类髋 OA 软骨的人类髋 OA 软骨的全面基因表达分析。我们的差异基因表达数据集与使用类似组织的类似定义研究具有极好的相关性,但在个体基因状态上显示髋和膝 OA 之间存在差异,但在涉及的分子途径上具有共性。