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

被引:28
|
作者
Watanabe, Kenichi [1 ]
Arumugam, Somasundaram [1 ]
Sreedhar, Remya [1 ]
Thandavarayan, Rajarajan A. [2 ]
Nakamura, Takashi [1 ]
Nakamura, Masahiko [3 ]
Harima, Meilei [1 ]
Yoneyama, Hiroyuki [4 ]
Suzuki, Kenji [5 ]
机构
[1] Niigata Univ Pharm & Appl Life Sci, Fac Pharmaceut Sci, Dept Clin Pharmacol, Niigata 9568603, Japan
[2] Houston Methodist Res Inst, Dept Cardiovasc Sci, Houston, TX 77030 USA
[3] Yamanashi Prefectural Cent Hosp, Dept Cardiol, Kofu, Yamanashi, Japan
[4] Stelic Inst & Co Inc, Minato City, Tokyo, Japan
[5] Niigata Univ, Grad Sch Med & Dent Sci, Dept Gastroenterol & Hepatol, Niigata, Japan
基金
日本科学技术振兴机构;
关键词
Experimental autoimmune myocarditis; Chronic heart failure; Cardiac remodeling; CHST15; siRNA; ACETYLGALACTOSAMINE; 4-SULFATE; 6-O-SULFOTRANSFERASE; CHONDROITIN SULFATE; HEART-FAILURE; PROTEOGLYCANS; MYOCARDITIS; COLLAGEN; DECORIN; EXPRESSION; CELLS; IDENTIFICATION;
D O I
10.1016/j.cellsig.2015.03.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1517 / 1524
页数:8
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