Song Dong-Yan, Huang Qiu-Hong, Zhou Bing-Rong, Xu Yang, Yin Zhi-Qiang, Permatasari Felicia, Luo Dan
Department of Dermatology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029; ; Department of Dermatology, The Affiliated Jiangyin Hospital of Southeast University Medical College, Jiangyin 214400, P.R. China.
Exp Ther Med. 2012 Aug;4(2):339-343. doi: 10.3892/etm.2012.586. Epub 2012 May 22.
To study the effects and mechanisms of Tanshinone IIA (Tan IIA) on the dihydrotestosterone (DHT)-induced expression of sterol regulatory element binding protein-1 (SREBP-1), the synthesis and secretion of lipids in HaCaT cells were examined. HaCaT cells were treated with DHT and Tan IIA at different concentrations. Real-time PCR was used to detect the expression of SREBP-1c, fatty acid synthase (FAS), acyl-CoA synthetase (ACS), stearoyl-CoA desaturase (SCD) and HMG-CoA reductase (HMGCR) mRNA in HaCaT cells. Western blotting was used to analyze the protein expression of SREBP-1 and phosphorylation of Akt. Flow cytometry and Nile red staining were used to detect the synthesis and secretion of lipids in HaCaT cells. We observed that Tan IIA inhibited the DHT-induced expression of SREBP-1 and p-AKT in HaCaT cells, which produced an effect similar to that of LY294002. Tan IIA significantly inhibited the transcription of lipid synthesis-related genes and decreased lipid secretion in HaCaT cells. In conclusion, Tan IIA downregulates the expression of lipid synthesis-related genes and decreases lipid secretion in HaCaT cells, which is correlated with the inhibitory effect on the DHT-induced mRNA and protein expression of SREBP-1 in HaCaT cells.
为研究丹参酮IIA(Tan IIA)对二氢睾酮(DHT)诱导的固醇调节元件结合蛋白-1(SREBP-1)表达的影响及其机制,检测了Tan IIA对HaCaT细胞脂质合成和分泌的影响。将HaCaT细胞用不同浓度的DHT和Tan IIA处理。采用实时定量PCR检测HaCaT细胞中SREBP-1c、脂肪酸合酶(FAS)、酰基辅酶A合成酶(ACS)、硬脂酰辅酶A去饱和酶(SCD)和3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)mRNA的表达。采用蛋白质免疫印迹法分析SREBP-1的蛋白表达及Akt的磷酸化水平。采用流式细胞术和尼罗红染色检测HaCaT细胞中脂质的合成和分泌。我们观察到Tan IIA抑制了DHT诱导的HaCaT细胞中SREBP-1和p-AKT的表达,其作用与LY294002相似。Tan IIA显著抑制HaCaT细胞中脂质合成相关基因的转录并减少脂质分泌。总之,Tan IIA下调HaCaT细胞中脂质合成相关基因的表达并减少脂质分泌,这与对DHT诱导的HaCaT细胞中SREBP-1的mRNA和蛋白表达的抑制作用相关。