...
首页> 外文期刊>Journal of atherosclerosis and thrombosis. >Insulin Suppresses HDL-Mediated Cholesterol Efflux from Macrophages Through Inhibition of Neutral Cholesteryl Ester Hydrolase and ATP-Binding Cassette Transporter G1 Expressions
【24h】

Insulin Suppresses HDL-Mediated Cholesterol Efflux from Macrophages Through Inhibition of Neutral Cholesteryl Ester Hydrolase and ATP-Binding Cassette Transporter G1 Expressions

机译:胰岛素通过抑制中性胆固醇酯水解酶和ATP结合盒式转运蛋白G1表达抑制巨噬细胞介导的胆固醇外流。

获取原文

摘要

Aims: We studied the effect of insulin on HDL-mediated cholesterol efflux from macrophages. The potential involvement of cholesteryl ester hydrolysis and membrane cholesterol transport was also addressed. Methods: Human monocyte-derived THP-1 cells were developed into macrophages. Cholesterol efflux was measured by incubating macrophages, labeled with [3H]-cholesterol, with HDL for 24 h. The cells were treated with insulin (0-500 nM) for 30 min prior to the addition of HDL. To investigate the molecular mechanisms of the effect of insulin, the expressions of neutral cholesteryl ester hydrolase (nCEH) and ATP-binding cassette transporter (ABC) G1 were analyzed. Results: Insulin inhibited, in a concentration-dependent manner, HDL-mediated cholesterol efflux from macrophages. Insulin also inhibited the enzyme activity of nCEH and its mRNA and protein expression in cells. Insulin also suppressed the expressions of mRNA and protein for ABCG1. Conclusions: Insulin inhibits HDL-mediated cholesterol efflux from macrophages, which may result from the suppression of nCEH and ABCG1 expressions. Our findings show part of the potential molecular mechanism of atherogenesis in type 2 diabetes with hyperinsulinemia.
机译:目的:我们研究了胰岛素对巨噬细胞从高密度脂蛋白介导的胆固醇外流的作用。还讨论了胆固醇酯水解和膜胆固醇转运的潜在作用。方法:将人单核细胞衍生的THP-1细胞发育为巨噬细胞。胆固醇外排通过将标有[ 3 H]-胆固醇的巨噬细胞与HDL孵育24小时来测量。在添加HDL之前,将细胞用胰岛素(0-500 nM)处理30分钟。为了研究胰岛素作用的分子机制,分析了中性胆固醇酯水解酶(nCEH)和ATP结合盒转运蛋白(ABC)G1的表达。结果:胰岛素以浓度依赖的方式抑制了HDL介导的巨噬细胞胆固醇排出。胰岛素还抑制nCEH的酶活性及其在细胞中的mRNA和蛋白质表达。胰岛素还抑制了ABCG1 mRNA和蛋白的表达。结论:胰岛素抑制巨噬细胞介导的HDL介导的胆固醇外流,这可能是由于nCEH和ABCG1表达的抑制所致。我们的发现显示了高胰岛素血症2型糖尿病中动脉粥样硬化的潜在分子机制的一部分。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号