首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Dipeptidyl peptidase-IV in synovial fluid and in synovial fluid mononuclear cells of patients with rheumatoid arthritis.
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Dipeptidyl peptidase-IV in synovial fluid and in synovial fluid mononuclear cells of patients with rheumatoid arthritis.

机译:类风湿关节炎患者滑液和滑液单核细胞中的二肽基肽酶-IV。

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摘要

BACKGROUND: Dipeptidyl peptidase-IV (DPP-IV) enzymatic activity controls biological halftime of multiple local mediators. Its deregulation is associated with pathogenesis of several autoimmune diseases, including rheumatoid arthritis (RA). Although DPP-IV is the canonical representative of the group, a number of other proteins have been shown to have similar enzymatic activity. This study was aimed to identify the molecular source of DPP-IV activity in synovial fluid (SF) and fluid mononuclear cells (FMNC) in patients with RA and osteoarthritis (OA). In addition, the association of DPP-IV and the concentration of stromal cell-derived factor-1alpha (SDF), DPP-IV substrate, were evaluated. METHODS: DPP-IV activity was measured by the kinetic fluorimetric method. The expression of studied molecules in FMNC and their concentrations in SF were assayed using flow cytometry and ELISA respectively. RESULTS: DPP-IV activity in SF, dominantly derived from the canonical DPP-IV, does not significantly differ between RA and OA. However, a significantly lower DPP-IV activity and expression in FMNC was found in RA as opposed to OA patients. Negative correlation between SDF concentration in SF and the relative amount of CD3+CD26+ cells was observed. CONCLUSIONS: We report decreased presence of DPP-IV/CD26 in CD3+ FMNC in RA, which also may participate on impaired balance of SDF concentration in SF.
机译:背景:二肽基肽酶-IV(DPP-IV)的酶活性控制着多个局部介体的生物学半衰期。它的失调与多种自身免疫性疾病的发病机理有关,包括类风湿性关节炎(RA)。尽管DPP-IV是该组的典型代表,但许多其他蛋白质已显示具有相似的酶促活性。本研究旨在确定RA和骨关节炎(OA)患者滑液(SF)和液体单核细胞(FMNC)中DPP-IV活性的分子来源。此外,评估了DPP-IV与基质细胞衍生因子-1α(SDF),DPP-IV底物的浓度之间的关系。方法:采用动力学荧光法测定DPP-IV的活性。分别使用流式细胞仪和ELISA法检测了FMNC中所研究分子的表达及其在SF中的浓度。结果:SF中的DPP-IV活性主要来自规范DPP-IV,RA和OA之间无显着差异。然而,与OA患者相反,RA中发现FMNC中的DPP-IV活性和表达明显降低。观察到SF中SDF浓度与CD3 + CD26 +细胞相对量之间呈负相关。结论:我们报道RA中CD3 + FMNC中DPP-IV / CD26的存在减少,这也可能参与了SF中SDF浓度平衡的损害。

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