福建医科大学学报
福建醫科大學學報
복건의과대학학보
JOURNAL OF FUJIAN MEDICAL UNIVERSITY
2013年
5期
271-273
,共3页
陈运新%黄月红%张莉娟%陈治新%王小众
陳運新%黃月紅%張莉娟%陳治新%王小衆
진운신%황월홍%장리연%진치신%왕소음
白细胞介素10%肝细胞%基因%基因表达%基因疗法%细胞因子类%血管内皮生长因子类
白細胞介素10%肝細胞%基因%基因錶達%基因療法%細胞因子類%血管內皮生長因子類
백세포개소10%간세포%기인%기인표체%기인요법%세포인자류%혈관내피생장인자류
interleukin-10%hepatocytes%genes%gene expression%gene therapy%cytokines%vas-cular endothelial grow th factors
目的:观察白细胞介素-10(IL-10)基因修饰对大鼠肝细胞增殖、凋亡的影响,并筛选出表达可能受影响的细胞因子。方法体外培养大鼠肝细胞系BRL ,分为对照组(C组),转染 pcDNA3.0空质粒(P组),转染pcDNA3.0-rIL-10重组质粒(I组)。M T T法检测其增殖,流式细胞法检测其凋亡,抗体芯片法检测其细胞因子的表达。结果转染48 h后,P组较C组增殖减少( P=0.000),凋亡增加( P=0.000);I组较P组增殖差别无统计学意义( P=0.279),但凋亡明显减少( P=0.000)。抗体芯片显示I组较P组除IL-10表达增加之外,血管表皮生长因子(VEGF)的表达下调。结论 IL-10基因治疗肝纤维化中,将肝细胞做为IL-10基因的表达细胞具有可行性。IL-10基因修饰后,肝细胞除了高表达IL-10之外,还通过下调VEGF的表达间接作用。
目的:觀察白細胞介素-10(IL-10)基因脩飾對大鼠肝細胞增殖、凋亡的影響,併篩選齣錶達可能受影響的細胞因子。方法體外培養大鼠肝細胞繫BRL ,分為對照組(C組),轉染 pcDNA3.0空質粒(P組),轉染pcDNA3.0-rIL-10重組質粒(I組)。M T T法檢測其增殖,流式細胞法檢測其凋亡,抗體芯片法檢測其細胞因子的錶達。結果轉染48 h後,P組較C組增殖減少( P=0.000),凋亡增加( P=0.000);I組較P組增殖差彆無統計學意義( P=0.279),但凋亡明顯減少( P=0.000)。抗體芯片顯示I組較P組除IL-10錶達增加之外,血管錶皮生長因子(VEGF)的錶達下調。結論 IL-10基因治療肝纖維化中,將肝細胞做為IL-10基因的錶達細胞具有可行性。IL-10基因脩飾後,肝細胞除瞭高錶達IL-10之外,還通過下調VEGF的錶達間接作用。
목적:관찰백세포개소-10(IL-10)기인수식대대서간세포증식、조망적영향,병사선출표체가능수영향적세포인자。방법체외배양대서간세포계BRL ,분위대조조(C조),전염 pcDNA3.0공질립(P조),전염pcDNA3.0-rIL-10중조질립(I조)。M T T법검측기증식,류식세포법검측기조망,항체심편법검측기세포인자적표체。결과전염48 h후,P조교C조증식감소( P=0.000),조망증가( P=0.000);I조교P조증식차별무통계학의의( P=0.279),단조망명현감소( P=0.000)。항체심편현시I조교P조제IL-10표체증가지외,혈관표피생장인자(VEGF)적표체하조。결론 IL-10기인치료간섬유화중,장간세포주위IL-10기인적표체세포구유가행성。IL-10기인수식후,간세포제료고표체IL-10지외,환통과하조VEGF적표체간접작용。
Objective To observe the effect of interleukin-10 gene modification on the prolifera-tion ,apoptosis and cytokine expression of rat hepatocye in vitro . Method BRL cells ,a normal rat hepa-tocyte line cultured in vitro , were divided into three groups ,group Cwas control group ,group Pwere transfected with plasmid pcDNA 3 .0 and group I with plasmid pcDNA 3 .0-rIL-10 .MTT assay ,flow cyto-metric analysis and cytokine antibody arrays were used to detect on the proliferation ,apoptosis and cyto-kine differential expression of BRL cells . Results Transfected with plasmid pcDNA3 .0 ,proliferation of BRL cells was inhibited ,and apoptosis was increased . This increase of apoptosis was attenuated in BRL cells of group I . Compare with group P ,BRL cells of group I showed a lower expression of vascular en-dothelial growth factor ,in addition to higher expression of IL-10 . Conclusion Hepatocytes are possible to be the ideal target cells of IL-10 gene transfer in the IL-10 gene therapy of liver fibrosis . T ransfected with IL-10 gene ,hepatocytes played an inhibitory role on liver fibrogenesis not only by high IL-10 produc-tion ,but also by low regulation on expression of vascular endothelial growth factor probably .