吉林大学学报(医学版) ›› 2019, Vol. 45 ›› Issue (01): 77-82.doi: 10.13481/j.1671-587x.20190115

• 基础研究 • 上一篇    

阿托伐他汀对HepG2细胞中脂代谢相关基因表达的影响

王艳丽, 黄鸣宇, 张鹏   

  1. 西安医学院病理学教研室, 陕西 西安 710021
  • 收稿日期:2018-04-15 发布日期:2019-01-28
  • 通讯作者: 张鹏,副教授(Tel:029-89549602,E-mail:zpeng3201@126.com) E-mail:zpeng3201@126.com
  • 作者简介:王艳丽(1976-),女,陕西省周至县人,主治医师,讲师,医学博士,主要从事动脉粥样硬化和脂代谢的分子病理学方面的研究。

Effects of atorvastatin on expression of lipid metabolism-related genes in HepG2 cells

WANG Yanli, HUANG Mingyu, ZHANG Peng   

  1. Department of Pathology, Xi'an Medical University, Xi'an 710021, China
  • Received:2018-04-15 Published:2019-01-28
  • Contact: 陕西省科技厅基金资助课题(2016SF-107);陕西省科技厅项目配套基金资助课题(2017PT33);西安医学院国家自然科学基金孵育项目资助课题(2017GJFY28);西安医学院博士科研启动基金资助课题(2016DOC25) E-mail:zpeng3201@126.com

摘要: 目的:探讨阿托伐他汀对HepG2细胞中载脂蛋白A1(apoA1)天然反义转录(apoA1-NAT)的作用及对脂代谢相关基因表达的影响。方法:采用不同浓度阿托伐他汀(0、1、10和100 nmol·L-1)干预HepG2细胞,0 nmol·L-1阿托伐他汀组为对照组,在不同时间点(6、12、24和48h)提取各组HepG2细胞总RNA,采用Real-time PCR法检测HepG2细胞中apoA1-NAT和脂代谢相关基因mRNA表达水平。结果:1和10 nmol·L-1阿托伐他汀组HepG2细胞形态正常。与6 h时比较,12、24和48h时10 nmol·L-1阿托伐他汀组HepG2细胞中apoA1-NAT表达水平明显降低(P<0.01),且呈明显的时间依赖性。在相同条件下,48h时HepG2细胞中apoA1 mRNA表达水平较6h时明显升高(P<0.01)。与对照组比较,100 nmol·L-1阿托代他汀组HepG2细胞中低密度脂蛋白受体(LDLR)、10 nmol·L-1阿托代他汀组HepG2细胞中清道夫受体B1(SRB1)及1和10 nmol·L-1阿托伐他汀组HepG2细胞中ATP结合盒式转运体A1(ABCA1)表达水平均有不同程度升高(P<0.01)。结论:阿托伐他汀通过抑制HepG2细胞中apoA1-NAT表达,促进脂代谢相关基因表达,进而促进胆固醇逆转运过程。

关键词: 阿托伐他汀, 载脂蛋白A1, 载脂蛋白A1天然反义转录, 脂代谢, HepG2细胞

Abstract: Objective: To explore the effects of atorvastatin on the natural antisense transcription of apolipoprotein A1 (apoA1-NAT) in the HepG2 cells and its influence in the expressions of lipid metabolism related genes.Methods: The HepG2 cells were intervened with different concentrations(0,1,10 and 100 nmol·L-1) of atorvastatin, and the 0 nmol·L-1 atorvastatin group was used as control group.The total RNA of HepG2 cells in various groups were extracted at different time points(6,12,24, and 48 h). The mRNA expression levels of lipid metabolism-related genes and apoA1-NAT expression levels were detected by Real-Time PCR method.Results: The morphology of HepG2 cells in 1 and 10 nmol·L-1 atorvastain groups was normal.Compared with 6 h, the expression levels of apoA1-NAT in the HepG2 cells in 10 nmol·L-1 atorvastatin group at 12, 24 and 48 h were significantly decreased (P<0.01) in a time-dependent manner. Under the same condition, the expression level of apoA1 mRNA in the HepG2 cells at 48 h was increased significantly compared with 6 h (P<0.01).Compared with control group, the expression levels of low density lipoprotein receptor(LDLR) in the HepG2 cells in 100 nmol·L-1 atorvastatin group,scavenger receptor-class B type 1 (SRB1) in 10 nmol·L-1 atorvastatin group and ATP binding cassette transporter A1(ABCA1) in 1 and 10 nmol·L-1 atorvastatin groups were increased(P<0.01) in different degrees.Conclusion: Atorvastatin can promote the expressions of lipid metabolism-related genes by inhibiting the expression of apoA1-NAT, and promote the process of reverse cholesterol transport.

Key words: atorvastatin, apolipoprotein A1, natural antisense transcription of apolipoprotein A1, lipid metabolism, HepG2 cells

中图分类号: 

  • R543.5