Mateescu Raluca G, Todhunter Rory J, Lust George, Burton-Wurster Nancy
Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, NY 14853, USA.
Biochem Biophys Res Commun. 2005 Jul 1;332(2):482-6. doi: 10.1016/j.bbrc.2005.04.144.
The biochemical mechanism for initiation of cartilage destruction in osteoarthritis (OA) is unknown but may involve as yet unidentified cartilage genes. The first evidence that MIG-6, a protein involved in signal transduction, is expressed in articular cartilage came from our recent in vitro microarray experiments using the Affymetrix canine GeneChip. Quantitative RT-PCR (q RT-PCR) confirmed a fourfold increase in MIG-6 mRNA in cartilage in response to mechanical impact in vitro. Our goal is to determine if MIG-6, which responds to mechanical impact, could have a role in the initiation of OA. We determined that mRNA transcript levels of MIG-6 were fourfold higher in degenerated cartilage from dogs with hip osteoarthritis than in disease-free cartilage from unaffected dogs and twofold higher than in the cartilage surrounding the lesion. This is the first report associating MIG-6 with OA. Additional studies will determine what role MIG-6 has in the origin of cartilage degeneration.
骨关节炎(OA)中软骨破坏起始的生化机制尚不清楚,但可能涉及尚未确定的软骨基因。有证据表明,参与信号转导的蛋白质MIG-6在关节软骨中表达,这一证据首次来自我们最近使用Affymetrix犬类基因芯片进行的体外微阵列实验。定量逆转录聚合酶链反应(q RT-PCR)证实,体外机械冲击后软骨中MIG-6 mRNA增加了四倍。我们的目标是确定对机械冲击有反应的MIG-6是否在OA的起始过程中发挥作用。我们确定,患有髋骨关节炎的犬类退化软骨中MIG-6的mRNA转录水平比未受影响犬类的无病软骨高四倍,比病变周围的软骨高两倍。这是第一份将MIG-6与OA相关联的报告。进一步的研究将确定MIG-6在软骨退变起源中所起的作用。