中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2013年
31期
2511-2515
,共5页
叶洁梅%吴原%黄金山%李偲俊%刘云
葉潔梅%吳原%黃金山%李偲俊%劉雲
협길매%오원%황금산%리시준%류운
RNA干扰%整合素β1%海马神经元%癫痫
RNA榦擾%整閤素β1%海馬神經元%癲癇
RNA간우%정합소β1%해마신경원%전간
RNA Interference%Integrin β1%Hippocampal neurons%Epilepsy
目的 构建大鼠整合素β1(integrin β1)基因RNA干扰慢病毒载体,为研究Sombati癫痫细胞模型integrin β1的作用机制提供载体.方法 构建integrin β1基因的4个shRNA慢病毒干扰载体,利用HEK 293T细胞进行慢病毒包装,感染靶细胞PC12,采用Western印迹验证干扰效果,筛选出沉默效果最好的慢病毒shRNA,感染新生大鼠海马神经元细胞和Sombati癫痫细胞,通过Western印迹检测其对海马神经元和Sombati癫痫细胞integrin β1的基因沉默效果.结果 经测序证实RNAi慢病毒载体构建成功,病毒达到有效滴度,PC12细胞病毒转染率达95%以上;Western印迹证实,重组慢病毒integrin β1 shRNA感染海马神经元细胞和Sombati癫痫细胞后integrin β1蛋白表达下降,integrinβ1 shRNA2重组慢病毒载体对海马神经元和Sombati癫痫细胞的沉默效率分别为70%和90%.结论 成功构建integrin β1 RNA干扰慢病毒载体,并在新生大鼠海马神经元和Sombati癫痫细胞中实现有效的基因沉默效应.
目的 構建大鼠整閤素β1(integrin β1)基因RNA榦擾慢病毒載體,為研究Sombati癲癇細胞模型integrin β1的作用機製提供載體.方法 構建integrin β1基因的4箇shRNA慢病毒榦擾載體,利用HEK 293T細胞進行慢病毒包裝,感染靶細胞PC12,採用Western印跡驗證榦擾效果,篩選齣沉默效果最好的慢病毒shRNA,感染新生大鼠海馬神經元細胞和Sombati癲癇細胞,通過Western印跡檢測其對海馬神經元和Sombati癲癇細胞integrin β1的基因沉默效果.結果 經測序證實RNAi慢病毒載體構建成功,病毒達到有效滴度,PC12細胞病毒轉染率達95%以上;Western印跡證實,重組慢病毒integrin β1 shRNA感染海馬神經元細胞和Sombati癲癇細胞後integrin β1蛋白錶達下降,integrinβ1 shRNA2重組慢病毒載體對海馬神經元和Sombati癲癇細胞的沉默效率分彆為70%和90%.結論 成功構建integrin β1 RNA榦擾慢病毒載體,併在新生大鼠海馬神經元和Sombati癲癇細胞中實現有效的基因沉默效應.
목적 구건대서정합소β1(integrin β1)기인RNA간우만병독재체,위연구Sombati전간세포모형integrin β1적작용궤제제공재체.방법 구건integrin β1기인적4개shRNA만병독간우재체,이용HEK 293T세포진행만병독포장,감염파세포PC12,채용Western인적험증간우효과,사선출침묵효과최호적만병독shRNA,감염신생대서해마신경원세포화Sombati전간세포,통과Western인적검측기대해마신경원화Sombati전간세포integrin β1적기인침묵효과.결과 경측서증실RNAi만병독재체구건성공,병독체도유효적도,PC12세포병독전염솔체95%이상;Western인적증실,중조만병독integrin β1 shRNA감염해마신경원세포화Sombati전간세포후integrin β1단백표체하강,integrinβ1 shRNA2중조만병독재체대해마신경원화Sombati전간세포적침묵효솔분별위70%화90%.결론 성공구건integrin β1 RNA간우만병독재체,병재신생대서해마신경원화Sombati전간세포중실현유효적기인침묵효응.
Objective To construct a recombinant lentiviral vector containing integrin β1 shRNA to provide an effective tool for integrin β1 gene effect and a possible mechanism of Sombati cell of clinical refractory epilepsy.Methods Four lentiviral vectors containing integrin β1 shRNA were constructed and transfected into 293T cells.PC12 cells were infected by concentrated lentivirus and the gene-silencing efficiency was verified.And the most effective lentivirus containing shRNA was selected with Western blot.Then neonatal rat hippocampal neurons and Sombati cells were infected by lentivirus containing shRNA and the gene-silencing efficiency was also monitored by Western blot.Results RNAi lentivirus expression vectors targeting rat integrin β1 gene were successfully constructed and confirmed by DNA sequencing.The recombinant lentivirus particles were packaged successfully to produce a sufficient titer for subsequent experiments.The expression of protein significantly decreased in rat hippocampal neurons and rat Sombati cells after vector transfection.Conclusion The recombinant lentiviral vector containing integrin β1 shRNA is constructed successfully.And the gene-silencing effects are effective and stable in neonatal rat hippocampal neurons and Sombati cells.