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Small interfering RNA therapy against carbohydrate sulfotransferase 15 inhibits cardiac remodeling in rats with dilated cardiomyopathy

机译:小分子干扰RNA疗法抗碳水化合物磺基转移酶15抑制扩张型心肌病大鼠心脏重构

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Carbohydrate sulfotransferase 15 (CHST15) is a sulfotransferase responsible for biosynthesis of chondroitin sulfate E (CS-E), which plays important roles in numerous biological events such as biosynthesis of proinflammatory cytokines. However, the effects of CHST15 siRNA in rats with chronic heart failure (CHF) after experimental autoimmune myocarditis (EAM) have not yet been investigated. CHF was elicited in Lewis rats by immunization with cardiac myosin, and after immunization, the rats were divided into two groups and treated with either CHST15 siRNA (2 mu g/week) or vehicle. Age matched normal rats without immunizations were also included in this study. After 7 weeks of treatment, we investigated the effects of CHST15 siRNA on cardiac function, proinflammatory cytokines, and cardiac remodeling in RAM rats. Myocardial functional parameters measured by hemodynamic and echocardiographic studies were significantly improved by CHST15 siRNA treatment in rats with CHF compared with that of vehicle-treated CHF rats. CHST15 siRNA significantly reduced cardiac fibrosis, and hypertrophy and its marker molecules (left ventricular (LV) mRNA expressions of transforming growth factor betal, collagens land III, and atrial natriuretic peptide) compared with vehicle-treated CHF rats. CHF-induced increased myocardial mRNA expressions of proinflammatory cytokines [interleukin (IL)-6, IL-1 beta], monocyte chemoattractant protein-1, and matrix metalloproteinases (MMP-2 and -9), and CHST15 were also suppressed by the treatment with CHST15 siRNA. Western blotting study has confirmed the results obtained from mRNA analysis as CHST5 siRNA treated rats expressed reduced levels of inflammatory and cardiac remodeling marker proteins. Our results demonstrate for the first time, that CHST15 siRNA treatment significantly improved LV function and ameliorated the progression of cardiac remodeling in rats with CHF after EAM. (C) 2015 Elsevier Inc. All rights reserved.
机译:碳水化合物磺基转移酶15(CHST15)是负责生物合成硫酸软骨素E(CS-E)的磺基转移酶,它在多种生物学事件(例如促炎性细胞因子的生物合成)中发挥重要作用。然而,尚未研究过CHST15 siRNA在实验性自身免疫性心肌炎(EAM)后对慢性心力衰竭(CHF)大鼠的影响。通过心脏肌球蛋白免疫在Lewis大鼠中诱发CHF,免疫后将大鼠分为两组,并用CHST15 siRNA(2μg /周)或溶媒治疗。年龄相匹配的未免疫的正常大鼠也包括在这项研究中。治疗7周后,我们调查了CHST15 siRNA对RAM大鼠心脏功能,促炎细胞因子和心脏重构的影响。通过CHST15 siRNA治疗,与载体治疗的CHF大鼠相比,通过CHST15 siRNA治疗可显着改善通过血液动力学和超声心动图研究测量的心肌功能参数。与载剂治疗的CHF大鼠相比,CHST15 siRNA显着降低了心脏纤维化,肥大及其标志物分子(转化生长因子betal,胶原蛋白III和心钠素的左心室(LV)mRNA表达)。 CHF诱导的促炎性细胞因子[白介素(IL)-6,IL-1β],单核细胞趋化蛋白1和基质金属蛋白酶(MMP-2和-9)和CHST15心肌mRNA表达的增加也受到抑制。 CHST15 siRNA。 Western印迹研究已证实,通过CHST5 siRNA处理的大鼠表达的炎症和心脏重塑标记蛋白水平降低,从而从mRNA分析获得了结果。我们的结果首次证明,CHST15 siRNA治疗可显着改善EAM后CHF大鼠的左室功能,并改善心脏重塑的进程。 (C)2015 Elsevier Inc.保留所有权利。

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