Friedman G, Stein O, Stein Y
Biochim Biophys Acta. 1978 Nov 22;531(2):222-32. doi: 10.1016/0005-2760(78)90146-7.
Lipoprotein lipase activity was studied in mesenchymal cells isolated from rat hearts and cultured for up to 8 days. The enzyme activity increased markedly between day 3 and 5 while the subsequent increase was less pronounced. Addition of hydrocortisone to complete culture medium resulted in an increase in lipoprotein lipase activity at all stages of culture. Lipoprotein lipase activity did not increase after addition of insulin to the complete culture medium. In the presence of serum-poor medium between day 3 and 6, the increase in lipoprotein lipase activity was much lower than in the presence of complete culture medium. Addition of hydrocortisone and insulin to the serum-poor medium resulted in a significant rise in lipoprotein lipase activity while less consistent effects were obtained after addition of each hormone alone. Transfer of cells to serum-poor medium between day 6 and 7 of culture caused a fall in enzyme activity. Addition of hydrocortisone alone and with insulin restored enzyme activity to control values. No effect on lipoprotein lipase was seen with estradiol, growth hormone, or glucagon when added to serum-containing medium, or serum-poor medium. These results indicate that the lipoprotein lipase of heart is controlled by glucocorticoids and that this control might require the presence of insulin for optimal expression.
对从大鼠心脏分离并培养长达8天的间充质细胞中的脂蛋白脂肪酶活性进行了研究。在第3天到第5天之间,该酶活性显著增加,而随后的增加则不太明显。向完全培养基中添加氢化可的松导致在培养的所有阶段脂蛋白脂肪酶活性增加。向完全培养基中添加胰岛素后,脂蛋白脂肪酶活性没有增加。在第3天到第6天存在低血清培养基时,脂蛋白脂肪酶活性的增加远低于存在完全培养基时。向低血清培养基中添加氢化可的松和胰岛素导致脂蛋白脂肪酶活性显著升高,而单独添加每种激素后得到的效果不太一致。在培养的第6天到第7天之间将细胞转移到低血清培养基中会导致酶活性下降。单独添加氢化可的松以及与胰岛素一起添加可使酶活性恢复到对照值。当添加到含血清培养基或低血清培养基中时,雌二醇、生长激素或胰高血糖素对脂蛋白脂肪酶没有影响。这些结果表明,心脏的脂蛋白脂肪酶受糖皮质激素控制,并且这种控制可能需要胰岛素的存在才能实现最佳表达。