Alejandre Maria José, Perales Sonia, Carazo Angel, Palomino-Morales Rogelio, Linares Ana
Department of Biochemistry and Molecular Biology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Lipids. 2006 Dec;41(12):1089-99. doi: 10.1007/s11745-006-5058-x.
The cyclic fluctuations of HMG-CoA reductase activity and mRNA are reportedly related to feeding the cells in culture or to variations in food consumption by the animals over a 24-h cycle. In this work, we demonstrate cyclic increments in HMG-CoA reductase activity in smooth muscle cells (SMC) not associated with the culture feeding. Since reductase activity also shows a marked rise preceding the S phase, one of the major goals of the present work was to evaluate this dual role of reductase activity and mRNA fluctuations related to the cell cycle and to food intake in the SMC-C/SMC-Ch cultures derived from control-fed (SMC-C) and cholesterol-fed (SMC-Ch) chicks. The period and amplitude oscillations in HMG-CoA reductase activity varied depending on culture conditions: lipoprotein-deficient serum vs. FBS, young vs. senescent cells, or confluent vs. nonconfluent cultures. The HMG-CoA reductase mRNA concentration showed a marked rise after feeding not correlated to the fluctuation activity, suggesting posttranscriptional modulation. Reductase activity and mRNA were down-regulated in SMC-Ch. Since the nutritional culture conditions were the same in both cell lines, these findings indicate that consumption of a high-cholesterol diet by the animals prior to the establishment of the SMC cultures induced changes in the HMG-CoA reductase gene expression in-aortic SMC.
据报道,HMG-CoA还原酶活性和mRNA的周期性波动与培养细胞的喂食情况或动物在24小时周期内食物摄入量的变化有关。在这项研究中,我们证明了平滑肌细胞(SMC)中HMG-CoA还原酶活性的周期性增加与培养物喂食无关。由于还原酶活性在S期之前也有显著升高,本研究的主要目标之一是评估还原酶活性和mRNA波动在与细胞周期以及来自对照喂养(SMC-C)和胆固醇喂养(SMC-Ch)小鸡的SMC-C/SMC-Ch培养物中的食物摄入相关的双重作用。HMG-CoA还原酶活性的周期和幅度振荡因培养条件而异:无脂蛋白血清与胎牛血清、年轻细胞与衰老细胞,或汇合培养与非汇合培养。喂食后HMG-CoA还原酶mRNA浓度显著升高,与波动活性无关,提示存在转录后调控。SMC-Ch中的还原酶活性和mRNA下调。由于两种细胞系的营养培养条件相同,这些发现表明在建立SMC培养物之前动物食用高胆固醇饮食会诱导主动脉SMC中HMG-CoA还原酶基因表达的变化。