靶向沉默HDAC6对乳鼠心房肌成纤维细胞活化增殖的作用 |
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引用本文: | 曹炜,石开虎,陶辉,施鹏,吴超,宣海洋,沙纪名,占红英. 靶向沉默HDAC6对乳鼠心房肌成纤维细胞活化增殖的作用[J]. 安徽医科大学学报, 2017, 52(3). DOI: 10.19405/j.cnki.issn1000-1492.2017.03.011 |
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作者姓名: | 曹炜 石开虎 陶辉 施鹏 吴超 宣海洋 沙纪名 占红英 |
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作者单位: | 安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601;安徽医科大学第二附属医院心胸外科,安徽医科大学心血管病研究中心,合肥 230601 |
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基金项目: | 安徽省高校自然科学研究项目,安徽省科技攻关项目 |
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摘 要: | 目的 探究组蛋白去乙酰化酶(HDAC6)对乳鼠心房肌成纤维细胞活化增殖的影响作用.方法 将50只乳鼠(雄性)分别提取心房肌成纤维细胞,应用Western blot法测定HDAC6和α-平滑肌肌动蛋白(α-SMA)的表达情况;运用qRT-PCR技术检测HDAC6和α-SMA mRNA的表达情况;MTT法检测心房肌成纤维细胞的细胞增殖活性;使用LipofectamineTM 2000 Reagent向心房肌成纤维细胞中转染小干扰RNA HDAC6(siRNA-HDAC6)后观察对心房肌成纤维细胞增殖的影响.结果 转染心房肌成纤维细胞siRNA-HDAC6组HDAC6和α-SMA的蛋白表达明显下降;qRT-PCR技术检测siRNA-HDAC6组中HDAC6和α-SMA的mRNA表达明显下降;转染siRNA-HDAC6明显抑制心房肌成纤维细胞的增殖活性.结论 靶向沉默HDAC6可抑制心房肌成纤维细胞活化增殖,提示其在心房纤维化中可能发挥调控作用.
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关 键 词: | 心房肌成纤维细胞 HDAC6 α-SMA |
The effect of HDAC6 silencing onproliferation in neonatal rat atrial fibroblasts |
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Abstract: | Objective To explore influence of histone deacetylase 6(HDAC6) on neonatal rat atrial fibroblasts activation and proliferation.Methods Atrial fibroblasts were treated with transforming growth factor-β1(TGF-β1) for 48 hours.qRT-PCR was applied to assess the expression of HDAC6 and α-smooth muscle actin(α-SMA) mRNA levels.The protein expression levels of HDAC6 and α-SMA were detected by Western blot.MTT assay was used to determine the proliferation of atrial fibroblasts.LipofectamineTM 2 000 Reagent was used to transfected atrial fibroblasts with siRNA-HDAC6.Results After cardiac fibroblasts transfected with siRNA-HDAC6, HDAC6 expression was declined and α-SMA expression was decreased.The atrial fibroblasts treated with TGF-β1 that HDAC6 expression was increased and α-SMA expression was increased.The activity of cardiac fibroblasts was decreased after transfected with siRNA-HDAC6.Conclusion HDAC6 can suppress proliferative activity of atrial fibroblasts markedly and could be a new therapeutic target of preventing atrial remodeling.The application of its regulator will provide the new idea and method for the prevention and cure of atrial fibrosis. |
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Keywords: | atrial fibroblasts histone deacetylase 6 α-smooth muscle actin |
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