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机构地区:[1]华中科技大学同济医学院附属同济医院泌尿外科,武汉430030
出 处:《临床泌尿外科杂志》2007年第2期143-145,共3页Journal of Clinical Urology
基 金:国家自然科学基金资助课题(No.30371423)
摘 要:目的:构建表达产甲酸草酸杆菌(Ox.F)草酸分解基因的人肝细胞系,探索高草酸尿的治疗方法。方法:分离培养人肠道Ox.F并克隆其功能基因oxc和frc,构建同时表达oxc和frc的真核双表达载体质粒pIRES-oxc-frc,将pIRES-oxc-frc转染人正常肝细胞系L-02。用RT-PCR和Western blot技术了解转基因细胞的目的基因表达状况;用离子色谱法测定转基因后细胞培养液中草酸浓度,了解其草酸分解功能。结果:转基因后人肝细胞系L-02在mRNA和蛋白质水平均成功表达oxc和frc基因,其草酸分解功能较转染前明显增强(P<0.01)。结论:Ox.F分解草酸的两个重要功能基因oxc和frc能在体外转入人正常肝细胞(L-02)中,并使后者草酸分解能力明显增强。转草酸分解基因的人肝细胞系的构建,有望用于高草酸尿,尤其是PH的病因治疗,值得进一步研究。Objective: To construct human hepatic cell line with oxalate-degradation genes from Oxalobacter formigenes, and explore the therapeutic method of hyperoxaluria. Methods:The Oxalobacter formigenes (Ox. F) from the human feces were isolated and cultured. The functional genes of the Ox. F-frc gene and oxc gene-were cloned. The dicistronic eukaryotic expression vector pIRES-oxc-frc was constructed. The normal human hepatic cell line(L-02 cells) were transfected with pIRES-oxc-frc. RT-PCR and Western blot were performed to detect the expression of the objective genes. The concentration of the oxalate in the culture medium which was used to culture the transgenic L-02 cells was determined by ion chromatography to explore the oxalate-degradation function of the transgenic L-02 cells. Results: After the gene transference, the oxc gene and frc gene could be expressed at mRNA and protein level in human hepatic cells (L-02 cells) successfully and the oxalate-degradation function of the cells increased( P 〈0.01). Conclusions:The two important functional genes of the Ox. F-frc gene and oxc gene-could be transfected into normal human hepatic cells(L-02 cells) in vitro successfully, and it increased the oxalate-degradation function of the latter. The successful construction of human hepatic cell line with oxalate-degradation genes might be used in the etilogical therapy of hyperoxaluria, especially primary hyperoxaluria , and is worth to be further studied.
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