Zhang Lei, He Qing-nan, Zhu Min, Zhou Gang, Ding Juan-juan, Zhou Pin, Wu Xiao-chuan, Yi Zhu-wen
Laboratory of Pediatric Nephrology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Dec;32(6):941-8.
To construct mesangial cell lines over- or under- expressing glucocorticoid receptor beta (GRbeta), to investigate the effect of GRbeta on glucocorticoid biological function, and to determine whether the overexpression of GRbeta explains the glucocorticoid-resistant in glomerular mesangial cells (GMCs).
The recombinant human sense or anti-sense gene of GRbeta was transferred into the rat GMCs by retrovirus-mediated stable transfection technique. Expression of hGRbeta mRNA in GMCs was determined by reverse transcription of total RNA followed by quantitative reverse transcription-polymerase chain reaction (RT-PCR), and the product of RT-PCR was then analyzed by gene sequencing. The expression of hGRbeta protein in GMCs was tested by Western blot. The inhibitory rate of dexamethasone-mediated cells on lipopolysaccharide (LPS)-stimulated GMC proliferation was detected to assess the effect of GRbeta at different expression levels on the glucocorticoid action. The cell proliferative activity in different cells with different levels of GRbeta was tested by MTT chromatometry. The change of cell cycle was analyzed by flow cytometry.
RT-PCR and gene sequencing showed that the recombinant sense and anti-sense genes were correctly integrated into genomic DNA of mesangial cells. The protein expression tested by Western blot showed that GRbeta in cells inserted with the sense hGRbeta gene was higher than those cells inserted with the anti-sense hGRbeta gene (109.74+/-10.63 vs. 19.08+/-1.01, P<0.05). The inhibitory rate of cell proliferation induced by dexamethasone was lower in GMCs transfected with sense hGRbeta gene than those transfected with anti-sense hGRbeta gene (18.47%+/-2.12% vs. 60.33%+/- 5.29%,P<0.05). Under the inhibition of dexamethasone, the decreased cell number of S-stage cells was significantly lower, and the increased cell number of G1- stage cells was significantly higher in GMCs transfected with sense hGRbeta gene than those of non-transfected cells.
The overexpression of GRbeta may inhibit the glucocorticoid action in GMCs. The GRbeta level in mesangial cells may be an important factor in determining whether they are sensitive or resistant to glucocorticoid.
构建过表达或低表达糖皮质激素受体β(GRβ)的系膜细胞系,研究GRβ对糖皮质激素生物学功能的影响,并确定GRβ的过表达是否可解释肾小球系膜细胞(GMCs)中的糖皮质激素抵抗。
采用逆转录病毒介导的稳定转染技术,将重组人GRβ正义或反义基因导入大鼠GMCs。通过总RNA逆转录后进行定量逆转录聚合酶链反应(RT-PCR)测定GMCs中hGRβ mRNA的表达,然后对RT-PCR产物进行基因测序。通过蛋白质免疫印迹法检测GMCs中hGRβ蛋白的表达。检测地塞米松介导的细胞对脂多糖(LPS)刺激的GMC增殖的抑制率,以评估不同表达水平的GRβ对糖皮质激素作用的影响。采用MTT比色法检测不同GRβ水平的细胞的增殖活性。通过流式细胞术分析细胞周期的变化。
RT-PCR和基因测序显示,重组正义和反义基因正确整合到系膜细胞的基因组DNA中。蛋白质免疫印迹法检测的蛋白表达显示,插入正义hGRβ基因的细胞中的GRβ高于插入反义hGRβ基因的细胞(109.74±10.63对19.08±1.01,P<0.05)。转染正义hGRβ基因的GMCs中,地塞米松诱导的细胞增殖抑制率低于转染反义hGRβ基因的细胞(18.47%±2.12%对60.33%±5.29%,P<0.05)。在地塞米松抑制下,转染正义hGRβ基因的GMCs中S期细胞数量的减少明显更低,G1期细胞数量的增加明显高于未转染细胞。
GRβ的过表达可能抑制GMCs中的糖皮质激素作用。系膜细胞中的GRβ水平可能是决定其对糖皮质激素敏感或抵抗的重要因素。