Ejtehadi H D, Freimanis G L, Ali H A, Bowman S, Alavi A, Axford J, Callaghan R, Nelson P N
Molecular Immunology Research Group, Research Institute in Healthcare Sciences, University of Wolverhampton, Wulfruna Street, Wolverhampton WV1 1SB, UK.
Ann Rheum Dis. 2006 May;65(5):612-6. doi: 10.1136/ard.2004.031146. Epub 2005 Sep 28.
To examine whether human endogenous retrovirus K10 is associated with autoimmune rheumatic disease.
A novel multiplex reverse transcription polymerase chain reaction (RT-PCR) system was developed to investigate HERV-K10 mRNA expression in patients with rheumatoid arthritis.
40 patients with rheumatoid arthritis, 17 with osteoarthritis, and 27 healthy individuals were recruited and total RNA was extracted from peripheral blood mononuclear cells (PBMCs) and analysed using multiplex RT-PCR for the level of HERV-K10 gag mRNA expression. Southern blot and DNA sequencing confirmed the authenticity of the PCR products.
Using the histidyl tRNA synthetase (HtRNAS) gene as a housekeeping gene in the optimised multiplex RT-PCR, a significantly higher level of HERV-K10 gag mRNA expression was found in rheumatoid arthritis than in osteoarthritis (p = 0.01) or in the healthy controls (p = 0.02).
There is enhanced mRNA expression of the HERV-K10 gag region in rheumatoid arthritis compared with osteoarthritis or healthy controls. This could contribute to the pathogenesis of rheumatoid arthritis.
研究人类内源性逆转录病毒K10是否与自身免疫性风湿性疾病相关。
开发了一种新型多重逆转录聚合酶链反应(RT-PCR)系统,以研究类风湿性关节炎患者中人类内源性逆转录病毒K10(HERV-K10)mRNA的表达情况。
招募了40例类风湿性关节炎患者、17例骨关节炎患者和27名健康个体,从外周血单个核细胞(PBMCs)中提取总RNA,并使用多重RT-PCR分析HERV-K10 gag mRNA的表达水平。Southern印迹和DNA测序证实了PCR产物的真实性。
在优化的多重RT-PCR中,使用组氨酰tRNA合成酶(HtRNAS)基因作为管家基因,发现类风湿性关节炎患者中HERV-K10 gag mRNA的表达水平明显高于骨关节炎患者(p = 0.01)或健康对照者(p = 0.02)。
与骨关节炎或健康对照相比,类风湿性关节炎患者中HERV-K10 gag区域的mRNA表达增强。这可能有助于类风湿性关节炎的发病机制。