Meng Juanhong, Ma Xuchen, Ma Dalong, Xu Caimin
Center for TMD & Orofacial Pain, School of Stomatology, Peking University, Beijing 100081, PR China.
Osteoarthritis Cartilage. 2005 Dec;13(12):1115-25. doi: 10.1016/j.joca.2005.03.010.
To identify the gene expression profile of mandibular condylar cartilage after experimentally induced osteoarthritis (OA).
We studied the gene expression levels in temporomandibular joint (TMJ) condylar cartilage during different stages of experimentally induced OA. The pathological characteristics of normal, early-stage and late-stage osteoarthritic TMJ cartilage were verified by histological techniques. The gene expression profiles in normal and osteoarthritic cartilage were measured by Affymetrix RAE230A microarrays. Some of the gene transcripts were confirmed by quantitative real-time reverse-transcription PCR analysis.
A comprehensive, differentially expressed, gene profile was obtained in TMJ cartilage during the progression of OA. In total, 138 genes and expressed sequence tags were up- or down-regulated at least 2-fold. Some of these genes have been shown to play a role in OA, including matrix-degrading proteases, protease inhibitors and genes involved in cell growth, apoptosis and bone remodeling. However, some genes that had never been reported to be related with OA, such as AQP3, SPP2, NOV, DKK3 and EGLN3, were consistently observed to be up-regulated in this study, suggesting they may be involved in OA progression.
This study provides a new gene expression profile of the progression of OA. Further study of these OA-related genes may provide new insights into understanding the molecular mechanisms underlying OA.
确定实验性诱导骨关节炎(OA)后下颌髁突软骨的基因表达谱。
我们研究了实验性诱导OA不同阶段颞下颌关节(TMJ)髁突软骨中的基因表达水平。通过组织学技术验证了正常、早期和晚期骨关节炎性TMJ软骨的病理特征。使用Affymetrix RAE230A微阵列测量正常和骨关节炎性软骨中的基因表达谱。通过定量实时逆转录PCR分析确认了一些基因转录本。
在OA进展过程中,TMJ软骨中获得了一个全面的、差异表达的基因谱。总共138个基因和表达序列标签上调或下调至少2倍。其中一些基因已被证明在OA中起作用,包括基质降解蛋白酶、蛋白酶抑制剂以及参与细胞生长、凋亡和骨重塑的基因。然而,一些从未被报道与OA相关的基因,如AQP3、SPP2、NOV、DKK3和EGLN3,在本研究中持续观察到上调,表明它们可能参与OA进展。
本研究提供了OA进展的新基因表达谱。对这些OA相关基因的进一步研究可能为理解OA潜在的分子机制提供新的见解。