Luo Wei, Lin Jieyi, Zhang Yi, Ouyang Jingyi, Mao Limei
Department of Nutrition and Food Hygiene, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China.
Wei Sheng Yan Jiu. 2013 Mar;42(2):245-9.
To explore the effects of oleic acid on the gene and protein expression of adiponectin and its PPARgamma mechanism in 3T3-l1 adipocytes.
L1 adipocytes were incubated with different concentration (25, 50, 100, 200, 400 micromol/L) for 24h, and the mRNA expression of adiponectin and PPARgamma was determined by real-time PCR (relative quantity). And then the 3T3-L1 adipocytes were treated for OA at concentration of 100 micromol/L for 24h with/without the affect of PPARgamma inhibitor GW9662, to determine the gene and protein expression of adiponectin. The protein expression changes of adiponectin were detected by immunoblotting.
The mRNA expression of adiponectin and PPARgamma increased at the dosages of 25, 50, and 100micromol /L. With the increase of OA, the mRNA expression of adiponectin and PPARgamma decreased in a dose-dependent manner. Incubating with GW9662 and OA, decreases in the mRNA and protein expression of adiponectin were 77% and 78.01% (P < 0.05), compared with the control respectively.
OA could increase the gene expression of adiponectin and PPARgamma mRNA in dose-dependent manner in 3T3-L1 adipocytes,which could be specifically blocked by GW9662, OA indues the expression of adiponectin mRNA and protein in 3T3-L1 adipocytes, possibly by a mechanism involving PPARgamma.
探讨油酸对3T3 - l1脂肪细胞中脂联素基因和蛋白表达的影响及其PPARγ机制。
将L1脂肪细胞与不同浓度(25、50、100、200、400微摩尔/升)孵育24小时,通过实时PCR(相对定量)测定脂联素和PPARγ的mRNA表达。然后在有或无PPARγ抑制剂GW9662影响的情况下,用100微摩尔/升的油酸处理3T3 - L1脂肪细胞24小时,以测定脂联素的基因和蛋白表达。通过免疫印迹检测脂联素的蛋白表达变化。
在25、50和100微摩尔/升剂量下,脂联素和PPARγ的mRNA表达增加。随着油酸浓度增加,脂联素和PPARγ的mRNA表达呈剂量依赖性下降。与对照组相比,与GW9662和油酸共同孵育时,脂联素的mRNA和蛋白表达分别下降了77%和78.01%(P < 0.05)。
油酸可使3T3 - L1脂肪细胞中脂联素基因表达和PPARγ mRNA呈剂量依赖性增加,但可被GW9662特异性阻断。油酸诱导3T3 - L1脂肪细胞中脂联素mRNA和蛋白表达,可能是通过涉及PPARγ 的机制实现的。