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miRNA-33对Hcy干预RAW264.7巨噬细胞衍生的泡沫细胞表达ABCA1/ABCG1的影响
引用本文:代佩,高奋,高宏伟,王远,冯高洁,张秦风,白瑞,秦卫伟,李虹,宋晓苏.miRNA-33对Hcy干预RAW264.7巨噬细胞衍生的泡沫细胞表达ABCA1/ABCG1的影响[J].中国病理生理杂志,2019,35(2):212-217.
作者姓名:代佩  高奋  高宏伟  王远  冯高洁  张秦风  白瑞  秦卫伟  李虹  宋晓苏
作者单位:山西医科大学第二医院心内科, 山西 太原 030001
基金项目:山西省自然科学基金资助项目(No.2014011040-3)
摘    要:目的:研究同型半胱氨酸(Hcy)是否通过微小RNA-33 (miRNA-33)抑制三磷酸腺苷结合盒转运体A1(ABCA1)和三磷酸腺苷结合盒转运体G1(ABCG1)的表达,从而降低胆固醇逆转运(RCT)效率。方法:复制RAW264.7巨噬细胞经氧化型低密度脂蛋白(ox-LDL)诱导为泡沫细胞的模型,油红O染色确定模型是否复制成功,用LipofectamineTM2000将miRNA-33 mimics和miRNA-33 inhibitor分别转染入细胞内,再给予5 mmol/L的Hcy干预24 h后进行实验;用油红O染色观察细胞内脂滴情况;real-time PCR和Western blot检测ABCA1和ABCG1的mRNA和蛋白表达水平;液体闪烁计数法检测细胞内胆固醇流出率;高效液相色谱分析细胞内胆固醇含量。结果:(1)与空白对照组相比,miRNA-33 mimics组细胞内脂滴含量增加,ABCA1和ABCG1的mRNA和蛋白表达量降低(P <0.05),细胞内胆固醇含量逐渐增加(P <0.05),细胞内胆固醇流出率逐渐减少(P <0.05);(2)与空白对照组相比,miRNA-33 inhibitor组检测结果与miRNA-33 mimics组的结果相反,差异具有统计学意义(P <0.05);(3)空白对照组、miRNA-33 mimics-NC组和miRNA-33 inhibitor-NC组3组间相比,所有检测结果的差异均无统计学显著性。结论:Hcy可间接通过诱导miRNA-33表达而抑制ABCA1和ABCG1的蛋白表达,降低RCT效率。

关 键 词:微小RNA-33  同型半胱氨酸  胆固醇逆转运  三磷酸腺苷结合盒转运体A1  三磷酸腺苷结合盒转运体G1
收稿时间:2018-02-26

Effect of miRNA-33 on ABCA1/ABCG1 expression in RAW264.7 macrophage-derived foam cells after Hcy treatment
DAI Pei,GAO Fen,GAO Hong-wei,WANG Yuan,FENG Gao-jie,ZHANG Qin-feng,BAI Rui,QIN Wei-wei,LI Hong,SONG Xiao-su.Effect of miRNA-33 on ABCA1/ABCG1 expression in RAW264.7 macrophage-derived foam cells after Hcy treatment[J].Chinese Journal of Pathophysiology,2019,35(2):212-217.
Authors:DAI Pei  GAO Fen  GAO Hong-wei  WANG Yuan  FENG Gao-jie  ZHANG Qin-feng  BAI Rui  QIN Wei-wei  LI Hong  SONG Xiao-su
Institution:Department of Cardiology, Second Hospital of Shanxi Medical University, Taiyuan 030001, China
Abstract:AIM:To study whether homocysteine (Hcy) inhibits the expression of ATP-binding cassette transporter A1 (ABCA1) and ATP-binding cassette transporter G1 (ABCG1) by microRNA-33 (miRNA-33) signaling, and reduces the efficiency of reverse cholesterol transport (RCT).METHODS:RAW264.7 macrophages were induced by oxidized low-density lipoprotein (ox-LDL) to establish foam cell model. Oil red O staining was used to determine whether the model was established successfully. miRNA-33 mimics and miRNA-33 inhibitor were transfected into the cells by Lipofectamine 2000, and the cells were exposed to Hcy at concentration of 5 mmol/L for 24 h. The intracellular lipid droplets were observed by Oil red O staining. The expression of ABCA1 and ABCG1 at mRNA and protein levels was determined by real-time PCR and Western blot. The cellular cholesterol content was analyzed by HPLC, and effluent rate of cholesterol was detected by the method of liquid scintillation counting.RESULTS:Compared with blank control group, the lipid content in miRNA-33 mimics group was increased, and the expression of ABCA1 and ABCG1 at mRNA and protein levels was decreased (P<0.05). The intracellular cholesterol content was increased gradually (P<0.05), and the cellular cholesterol efflux rate was gradually decreased (P<0.05) in miRNA-33 mimics group. Compared with blank control group, the testing results in miRNA-33 inhibitor group were the opposition of those in miRNA-33 mimics group (P<0.05). No diffe-rence of the above indexes among blank control group, miRNA-33 mimics-NC group and miRNA-33 inhibitor-NC group was observed.CONCLUSION:Hcy inhibits the mRNA and protein expression of ABCA1 and ABCG1 through miRNA-33 signaling, and reduces the efficiency of RCT in RAW264.7 macrophage-derived foam cells.
Keywords:MicroRNA-33  Homocysteine  Cholesterol reverse transport  ATP binding cassette transporter A1  ATP binding cassette transporter G1
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