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作 者:陈杰[1] 赵立子[1] 邓颖[1] 王雪丁[1] 关溯[1] 黄民[1]
机构地区:[1]中山大学临床药理研究所,广东省广州510080
出 处:《中国基层医药》2006年第4期543-545,共3页Chinese Journal of Primary Medicine and Pharmacy
摘 要:目的研究质粒表达型短发夹RNA(smallhairpinRNA,shRNA)对CHL-3A4转基因细胞的细胞色素P4503A4(cytochromeP4503A4,CYP3A4)基因表达的影响。方法设计并构建3条shRNA真核表达载体(CYP3A4Ⅰ、CYP3A4Ⅱ、CYP3A4Ⅲ),脂质体转染CHL-3A4转基因细胞。转染48h后,TR-PCR和WesternBlotting分别观察3条shRNA对CYP3A4mRNA和蛋白表达的影响;噻唑蓝(MTT)观察shRNA抑制环磷酰胺对CHL-3A4转基因细胞毒性作用。结果CYP3A4Ⅲ表达载体的shRNA分别能抑制CHL-3A4细胞的CYP3A4mRNA表达(70%)及蛋白表达(75%),抑制环磷酰胺对CHL-3A4细胞(75%)细胞毒作用。结论RNA干扰能显著抑制CYP3A4基因的表达,RNA干扰技术为肝细胞色素P450的研究提供了新的方法。Objective To investigate the inhibitory effect of the eytoehrome P450 3A4(CYP3A4) gene expression and function in CHL-3A4 cells lines by vector-eepressed small hairpin interfering RNA(shRNA). Methods The shRNA expression vectors targeting CYP 3A4 gene( CYP3A4 Ⅰ , CYP3A4 Ⅱ , CYP3A4 Ⅲ ) were designed and constructed. The inhibitory effect of shRNA was detected by Western blot and RT-PCR analysis. The inhibitory effect of cytotoxie of cyclophosphamide using shRNA was measured by MTT assay. Results CYP3A4 Ⅲ shRNA expressing vector significantly reduced the CYP3A4 mRNA (70%) and protein expression levels (75 % ) of the CYP3A4 gene in CHL3A4 cells suppression of CYP3A4 gene expression by CYP3A4 Ⅲ largely reversed cyclophosphamide cytotoxieity(75 % ) in CHL-3A4 cells. Conclusion Vector-based RNAi could suppress CYP3A4 gene expression and function,and the use of RNAi to inhibit CYP3A4 gene expression in mammalian cells was a promising new tool for the study of cytoehrome P450 gene function.
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