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作 者:徐丽[1] 郭立平[1] 朱淼[1] 高雪[1] 张路培[1] 高会江[1] 李俊雅[1] 许尚忠[1]
机构地区:[1]中国农业科学院北京畜牧兽医研究所,农业畜禽遗传资源与利用重点开放实验室,北京100193
出 处:《中国畜牧兽医》2013年第5期133-139,共7页China Animal Husbandry & Veterinary Medicine
基 金:“十二五”国家科技支撑计划“优质肉牛新品种(系)选育与关键技术研究及示范(2011BAD28B04)”;所基本科研业务费专项资金项目“基于高密度SNP建立中国肉牛群体全基因组选择优化方案(2010jc-2)”;农业部专项“现代农业(肉牛)产业技术体系岗位科学家(CARS-38)”
摘 要:为了研究固醇调节元件结合蛋白(sterol regulatory element binding factor 1,SREBP1)基因的表达与细胞脂肪形成的关系,本研究构建了pEGFP-C1-SREBP1重组质粒,利用脂质体介导法将重组质粒pEGFP-C1-SREBP1及pEGFP-C1空质粒转染至牛胎儿骨骼肌成纤维细胞培养48h,实时荧光定量PCR和Western blotting分析目标基因表达水平的变化,并采用油红O染色检测细胞内脂滴。结果发现,pEGFP-C1-SREBP1重组质粒转染细胞内SREBP1mRNA的表达水平显著高于空白对照组和阴性对照组(P<0.05);SREBP1蛋白也出现明显上调;空白对照组和pEGFP-C1阴性对照组细胞内均未见有红染细胞,而pEGFP-C1-SREBP1重组质粒转染组中出现了清晰的红染细胞。说明SREBP1的表达可促进牛胎儿骨骼肌成纤维细胞脂肪合成,证实牛胎儿成纤维细胞中SREBP1表达和脂滴形成之间存在直接关系。The objective of this study was to investigate the relationship between sterol regulatory element binding factor 1(SREBP1) gene expression and cell fat formation,recombinant plasmid pEGFP-C1-SREBP1 was constructed and transferred into bovine fetal fibroblasts with Lipofectamine 2000,and then the cells were cultured for 48 h.Furthermore,the expressions of SREBP1 mRNA and protein were detected by Real-time PCR and Western blotting.Oil red O staining was used to explore cellular lipid droplet formation.The results showed that an up-regulation of SREBP1 mRNA in recombinant plasmid transfection group compared with normal control group and pEGFP-C1 transfected group,SREBP1 protein also appeared obvious rise.Oil red O found no lipid droplet in normal control group and pEGFP-C1 transfected group,but marked lipid droplets were detected in pEGFP-C1-SREBP1 transfected group.In conclusion,the up-regulation of SREBP1 directly resulteds in cellular lipid droplet formation in bovine fetal fibroblasts.
关 键 词:固醇调节元件结合蛋白 过表达 牛胎儿成纤维细胞 脂滴形成 质粒转染
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