首页> 外文期刊>International Journal of Cardiology >Calreticulin overexpression correlates with integrin-α5 and transforming growth factor-β1 expression in the atria of patients with rheumatic valvular disease and atrial fibrillation
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Calreticulin overexpression correlates with integrin-α5 and transforming growth factor-β1 expression in the atria of patients with rheumatic valvular disease and atrial fibrillation

机译:风湿性瓣膜病合并心房颤动患者心房钙网蛋白过表达与整合素α5和转化生长因子β1的表达相关

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Objectives The aim of this study was to determine whether altered calreticulin expression and distribution contribute to the pathogenesis of atrial fibrillation (AF) associated with valvular heart disease (VHD). Background AF affects electrophysiological and structural changes that exacerbate AF. Atrial remodeling reportedly underlies AF generation, but the precise mechanism of atrial remodeling in AF remains unclear. Methods Right and left atrial specimens were obtained from 68 patients undergoing valve replacement surgery. The patients were divided into sinus rhythm (SR; n = 25), paroxysmal AF (PaAF; n = 11), and persistent AF (PeAF; AF lasting > 6 months; n = 32) groups. Calreticulin, integrin-α5, and transforming growth factor-β1 (TGF-β1) mRNA and protein expression were measured. We also performed immunoprecipitation for calreticulin with either calcineurin B or integrin-α5. Results Calreticulin, integrin-α5, and TGF-β1 mRNA and protein expression were increased in the AF groups, especially in the left atrium in patients with mitral valve disease. Calreticulin interacted with both calcineurin B and integrin-α5. Integrin-α5 expression correlated with TGF-β1 expression, while calreticulin expression correlated with integrin-α5 and TGF-β1 expression. Despite similar cardiac function classifications, calreticulin expression was greater in the PeAF group than in the SR group. Conclusions Calreticulin, integrin-α5, and TGF-β1 expression was increased in atrial tissue in patients with AF and was related to AF type, suggesting that calreticulin is involved in the pathogenesis of AF in VHD patients.
机译:目的这项研究的目的是确定钙网蛋白表达和分布的改变是否有助于与瓣膜性心脏病(VHD)相关的房颤(AF)的发病机理。背景房颤会影响加剧房颤的电生理和结构变化。据报道,心房重构是房颤发生的基础,但房颤中房颤重构的确切机制仍不清楚。方法从68例接受瓣膜置换手术的患者获得左右心房标本。将患者分为窦律(SR; n = 25),阵发性AF(PaAF; n = 11)和持续性AF(PeAF; AF持续> 6个月; n = 32)组。测量了钙网蛋白,整联蛋白-α5和转化生长因子-β1(TGF-β1)mRNA和蛋白质表达。我们还用钙调神经磷酸酶B或整联蛋白-α5对钙网蛋白进行了免疫沉淀。结果房颤组,尤其是二尖瓣病变患者左心房中钙网蛋白,整联蛋白-α5和TGF-β1的mRNA和蛋白表达增加。钙网蛋白与钙调神经磷酸酶B和整联蛋白-α5相互作用。整联蛋白-α5表达与TGF-β1表达相关,而钙网蛋白表达与整联蛋白-α5和TGF-β1表达相关。尽管有相似的心脏功能分类,但PeAF组的钙网蛋白表达高于SR组。结论房颤患者心房组织中钙网蛋白,整联蛋白-α5和TGF-β1的表达升高,且与房颤类型有关,提示钙网蛋白参与了VHD患者房颤的发病机制。

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