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缺氧诱导因子-1α小干扰RNA对HaCaT细胞VEGF表达的影响
引用本文:李勇坚,祖旭宇,张桂英,肖嵘,文海泉. 缺氧诱导因子-1α小干扰RNA对HaCaT细胞VEGF表达的影响[J]. 中华皮肤科杂志, 2011, 44(9). DOI: 10.3760/cma.j.issn.0412-4030.2011.09.017
作者姓名:李勇坚  祖旭宇  张桂英  肖嵘  文海泉
作者单位:1. 南华大学附属第一医院皮肤科, 湖南衡阳,421001
2. 临床研究所
3. 中南大学湘雅二医院皮肤科
基金项目:湖南省卫生厅科研基会项目,衡阳市2010年科学技术发展计划项目
摘    要:目的 探讨缺氧诱导因子-1α( HIF-1α )RNA干扰对低氧条件下HaCaT细胞HIF -1α和血管内皮细胞生长因子(VEGF)表达的影响。方法 将HaCaT细胞分为4组:常氧对照组(无干预因素)、低氧组(缺氧培养24h)、脂质体对照组(转染空载脂质体后缺氧培养24h)、RNA干扰组(转染脂质体介导的RNA干扰序列后缺氧培养24 h)。荧光实时定量PCR法检测各组HaCaT细胞HIF-1α和VEGF mRNA表达水平,Western印迹检测各组HaCaT细胞HIF-1α和VEGF蛋白表达水平。结果 低氧组和常氧对照组HIF-1α mRNA的表达水平分别为0.907±0.032和0.878±0.034,两者比较差异无统计学意义(F=1.108,P>0.05),而低氧组VEGF mRNA和HIF-1α及VEGF蛋白的表达水平分别为0.935±0.032和0.813±0.047,0.791±0.030,均较常氧对照组(分别为0.652±0.053、0.236±0.014和0.316±0.013)明显增高(P值均< 0.05);RNA干扰组HIF-1α mRNA及蛋白的表达水平为0.230±0.044和0.213±0.026,VEGF为0.497±0.033和0.249±0.028,均较脂质体对照组(分别为0.978±0.030、0.817±0.049和0.806±0.040、0.833±0.052)显著降低(P值均<0.05)。结论 低氧可以使HaCaT细胞HIF-1α和VEGF的表达增加,而抑制HIF-1α的表达可以使低氧条件下HaCaT细胞VEGF的表达减少。

关 键 词:角蛋白细胞  缺氧诱导因子1,α亚基  RNA干扰  血管内皮生长因子类

Effects of hypoxia inducible factor-1 alpha-targeting small interfering RNA on vascular endothelial growth factor gene expression in HaCaT cells
LI Yong-jian,ZU Xu-yu,ZHANG Gui-ying,XIAO Rong,WEN Hai-quan. Effects of hypoxia inducible factor-1 alpha-targeting small interfering RNA on vascular endothelial growth factor gene expression in HaCaT cells[J]. Chinese Journal of Dermatology, 2011, 44(9). DOI: 10.3760/cma.j.issn.0412-4030.2011.09.017
Authors:LI Yong-jian  ZU Xu-yu  ZHANG Gui-ying  XIAO Rong  WEN Hai-quan
Abstract:Objective To observe the effects of hypoxia inducible factor-1 alpha (HIF-1α)-targeting small interfering RNA (siRNA) on the expression of HIF-1α and vascular endothelial growth factor (VEGF) in HaCaT ceils under hypoxic conditions. Methods HaCaT cells were cultured and divided into four groups, normal control group (without any treatment), hypoxia group (cultured under hypoxic conditions for 24 hours),liposome control group (transfected with liposome followed by hypoxic culture for 24 hours), RNA interference group (transfected with HIF-1α-targeting siRNA/liposome complexes followed by hypoxic culture for 24 hours). Fluorescence real-time quantitative PCR was utilized to determine HIF-1oα and VEGF mRNA expression in HaCaT cells, and Western blot to detect HIF-1α and VEGF protein expression. Results No significant difference was observed in the mRNA expression of HIF-1α between the hypoxia group and normal control group (0.907 ± 0.032 vs. 0.878 ± 0.034, F =1.108, P > 0.05), while the expression levels of VEGF mRNA,HIF-1α and VEGF proteins were significantly higher in the hypoxia group than in the normal control group (0.935 ± 0.032 vs. 0.652 ± 0.053, 0.813 ± 0.047 vs. 0.236 ± 0.014, 0.791 ± 0.030 vs. 0.316 ± 0.013, all P <0.05). A significant decline was noted in the mRNA and protein expression levels of VEGF (0.230 ± 0.044 vs.0.978 ± 0.030, 0.213 ± 0.026 vs. 0.817 ± 0.049, both P < 0.05) and HIF-1α (0.497 ± 0.033 vs. 0.806 ±0.040, 0.249 ± 0.028 vs. 0.833 ± 0.052, both P < 0.05) in the RNA interference group than in the liposome control group. Conclusions Hypoxia may enhance the expression of HIF-1α and VEGF in HaCaT cells, and to inhibit the HIF-1α expression may suppress the expression of VEGF in HaCaT cells under hypoxia.
Keywords:Keratinocytes  Hypoxia-inducible factor,alpha subunit  RNA interference  Vascular endothelial growth factors
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