Kevorkian Lara, Young David A, Darrah Clare, Donell Simon T, Shepstone Lee, Porter Sarah, Brockbank Sarah M V, Edwards Dylan R, Parker Andrew E, Clark Ian M
University of East Anglia, Norwich, UK.
Arthritis Rheum. 2004 Jan;50(1):131-41. doi: 10.1002/art.11433.
To profile the expression of all known members of the matrix metalloproteinase (MMP), ADAMTS, and tissue inhibitor of metalloproteinases (TIMP) gene families in normal cartilage and cartilage from patients with osteoarthritis (OA).
Human cartilage was obtained from femoral heads at joint replacement for OA or following fracture to the femoral neck. Total RNA was purified, and gene expression was assayed using quantitative real-time polymerase chain reaction.
Several members of the above gene families were regulated in OA. Genes that showed increased expression in OA were MMP13, MMP28, and ADAMTS16 (all at P < 0.001), MMP9, MMP16, ADAMTS2, and ADAMTS14 (all at P < 0.01), and MMP2, TIMP3, and ADAMTS12 (all at P < 0.05). Genes with decreased expression in OA were MMP1, MMP3, and ADAMTS1 (all at P < 0.001), MMP10, TIMP1, and ADAMTS9 (all at P < 0.01), and TIMP4, ADAMTS5, and ADAMTS15 (all at P < 0.05). Correlation analysis revealed that groups of genes across the gene families were coexpressed in cartilage.
This is the first comprehensive expression profile of all known MMP, ADAMTS, and TIMP genes in cartilage. Elucidation of patterns of expression provides a foundation with which to understand mechanisms of gene regulation in OA and potentially to refine the specificity of antiproteolytic therapies.
分析基质金属蛋白酶(MMP)、含血小板反应蛋白基序的解聚素样金属蛋白酶(ADAMTS)和金属蛋白酶组织抑制剂(TIMP)基因家族所有已知成员在正常软骨和骨关节炎(OA)患者软骨中的表达情况。
从因OA行关节置换术的股骨头或股骨颈骨折患者处获取人软骨。纯化总RNA,并使用定量实时聚合酶链反应检测基因表达。
上述基因家族的几个成员在OA中受到调控。在OA中表达增加的基因有MMP13、MMP28和ADAMTS16(均P < 0.001),MMP9、MMP16、ADAMTS2和ADAMTS14(均P < 0.01),以及MMP2、TIMP3和ADAMTS12(均P < 0.05)。在OA中表达降低的基因有MMP1、MMP3和ADAMTS1(均P < 0.001),MMP10、TIMP1和ADAMTS9(均P < 0.01),以及TIMP4、ADAMTS5和ADAMTS15(均P < 0.05)。相关性分析显示,基因家族中的几组基因在软骨中共同表达。
这是软骨中所有已知MMP、ADAMTS和TIMP基因的首个全面表达谱。对表达模式的阐释为理解OA中的基因调控机制以及潜在地优化抗蛋白水解疗法的特异性提供了基础。