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作 者:孙桦[1] 李光明[1] 虢灿杰[1] 刘博伟[1] 胡俊杰[1] 李定国[1]
机构地区:[1]上海交通大学医学院附属新华医院消化内科,上海200092
出 处:《胃肠病学和肝病学杂志》2008年第9期758-761,共4页Chinese Journal of Gastroenterology and Hepatology
摘 要:目的研究小干扰RNA(shRNA)重组载体介导抑制大鼠肝星状细胞(hepaticstellatecell,HSC)bcl-2基因的表达,初步观察其对HSC生物活性的影响。方法设计有小发夹结构的3条DNA序列构建重组质粒载体pGPU6-GFP,脂质体转染HSC—T6细胞株以荧光定量PCR和Westernblot筛选鉴定,通过CCK-8法及AnnexinV/PI双标记流式细胞术检测、观察其对HSC生长的影响。结果pGPU6-GFP—shRNA1、shRNA2均能抑制bcl-2mRNA和蛋白表达(P〈0.05),pGPU6-GFP—shRNAl转染HSC.T6株72h后对bcl-2基因抑制达80%,且HSC—T6体外生长明碌受到抑制,早期凋亡率为33.34%~44.12%。结论bel-2小发夹RNA重组载体shRNA1能最有效抑制HSC—T6中bcl-2的表达与细胞生长,促进凋亡,为下一步探索肝纤维化基因治疗提供实验依据。Objective To investigate the effect of small hairpin RNA (shRNA) targeting bcl-2 gene on the bcl-2 expression and the biological behaviors of hepatic stellate cells (HSCs). Methods Three designed DNA sequences with small hairpin structure were cloned into the transeripted carrier pGPU6-GFP which was transfected into HSC-T6 by lipofectamine. The expression of bcl-2 was screened by real-time PCR and Western blot. The cell proliferation was assayed by CCK-8 method and the cell apoptosis by flow cytometry. Results pGPU6-GFP-shRNA1 , shRNA2 could inhibit the expression bcl-2 mRNA and protein (P 〈 0.05) , pGPU6-GFP-shRNA1 of which was the most effective one with 80% inhibition rate, significantly decreasing the proliferating activity of HSC ( P 〈 0.05 ) , but increasing the apoptosis rate 33.34% -44.12%. Conclusion The constructed bcl-2 shRNA expressing plasmid of pGPU6-GFP-shRNA1 an reduce the expression of bcl-2 at maximum, inhibit the proliferation of HSC and induce apoptosis. Experimental basis is provided for gene therapy of liver fibrosis.
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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