Sjöberg A, Oscarsson J, Boström K, Innerarity T L, Edén S, Olofsson S O
Department of Medical Biochemistry, University of Göteborg, Sweden.
Endocrinology. 1992 Jun;130(6):3356-64. doi: 10.1210/endo.130.6.1597147.
Apolipoprotein-B 48 (apoB 48) and apoB 100 expression and the editing of apoB mRNA have previously been shown to be hormonally regulated in rat liver. We have investigated the effects of hypophysectomy and replacement therapy with T4, cortisol (C), and GH in vivo on the proportion of edited apoB mRNA in rat liver and cultured rat hepatocytes as well as the synthesis and secretion of apoB 48 and apoB 100 in cultured rat hepatocytes. Hypophysectomy decreased the proportion of edited apoB mRNA in intact liver from 62% in normal rats to 29% in hypophysectomized rats. Treatment of hypophysectomized rats with T4 and C did not influence the proportion of edited apoB mRNA, whereas treatment with GH, either alone or together with T4 and C, increased the proportion of edited apoB mRNA to the levels observed in normal rats. In cultured hepatocytes isolated from normal rats, the proportion of apoB 48 (percentage of total labeled apoB) was 78% and decreased to 40% in cells isolated from hypophysectomized rats. Treatment of hypophysectomized rats with T4 and C had no effect on the proportion of apoB 48 present in isolated cells, whereas it increased to 60% after treatment with GH together with T4 and C. The proportion of apoB 48 in the medium was affected by hypophysectomy and the various hormonal treatments in a similar way to that observed in the cells. Results from in vivo labeling experiments suggested that GH alone had the capacity to increase the percentage of apoB 48 in hypophysectomized rats. On the contrary, T4 and C was needed, in addition to GH, to increase the proportion of apoB 48 in isolated hepatocytes from hypophysectomized rats. Our results suggest that this discrepancy is due to a difference between the effect of GH alone on apoB mRNA editing in the intact liver and that in isolated hepatocytes. The total secretion of apoB into the cell culture medium was not affected by hypophysectomy and hormonal treatments of the rats. In conclusion, these results indicate that GH is involved in the regulation of editing of apoB mRNA and the proportion of apoB 48 synthesized and secreted in rat liver. Thus, our observations emphasize the importance of GH as a regulator of lipoprotein metabolism.
载脂蛋白B48(apoB 48)和apoB 100的表达以及apoB mRNA的编辑此前已被证明在大鼠肝脏中受到激素调节。我们研究了垂体切除及用甲状腺素(T4)、皮质醇(C)和生长激素(GH)进行体内替代治疗对大鼠肝脏及培养的大鼠肝细胞中apoB mRNA编辑比例的影响,以及对培养的大鼠肝细胞中apoB 48和apoB 100合成与分泌的影响。垂体切除使完整肝脏中编辑后的apoB mRNA比例从正常大鼠的62%降至垂体切除大鼠的29%。用T4和C治疗垂体切除的大鼠对编辑后的apoB mRNA比例没有影响,而单独用GH治疗或与T4和C联合治疗,可使编辑后的apoB mRNA比例增加到正常大鼠中观察到的水平。在从正常大鼠分离的培养肝细胞中,apoB 48的比例(占总标记apoB的百分比)为78%,而从垂体切除大鼠分离的细胞中该比例降至40%。用T4和C治疗垂体切除的大鼠对分离细胞中apoB 48的比例没有影响,而在与T4和C联合用GH治疗后该比例增加到60%。培养基中apoB 48的比例受垂体切除及各种激素治疗的影响,其方式与在细胞中观察到的类似。体内标记实验结果表明,单独使用GH有能力增加垂体切除大鼠中apoB 48的百分比。相反,除了GH之外,还需要T4和C来增加从垂体切除大鼠分离的肝细胞中apoB 48的比例。我们的结果表明,这种差异是由于单独使用GH对完整肝脏和分离肝细胞中apoB mRNA编辑的影响不同所致。apoB向细胞培养基中的总分泌不受大鼠垂体切除及激素治疗的影响。总之,这些结果表明GH参与了大鼠肝脏中apoB mRNA编辑以及apoB 48合成与分泌比例的调节。因此,我们的观察结果强调了GH作为脂蛋白代谢调节因子的重要性。