Philippe J
Department of Microbiology, Centre Médical Universitaire, Geneva, Switzerland.
J Clin Invest. 1989 Aug;84(2):672-7. doi: 10.1172/JCI114214.
Complex interrelationships exist between the four pancreatic islet cell types and their respective secretory products, insulin, glucagon, somatostatin, and pancreatic polypeptide. These hormones are known to interact with the different islet cells and modulate their functions. Insulin inhibits glucagon secretion from the A cell both in vivo and in vitro and, in states of insulin deficiency, high glucagon levels are observed that are normalized by insulin replacement. To determine if insulin also regulates glucagon biosynthesis, we studied its effects on glucagon gene expression. Our studies indicate that insulin, in a dose-dependent fashion decreases steady-state glucagon mRNA levels in a clonal hamster islet cell line, In-R1-G9; this decrease is secondary to an inhibition of glucagon gene transcription as assessed by transcriptional run-on assays and does not involve detectable changes in mRNA stability. Inhibition of glucagon gene transcription is accompanied by corresponding decreases in glucagon immunoreactivity in both cell extracts and medium. We conclude that insulin may not only regulate glucagon secretion but also glucagon gene expression.
四种胰岛细胞类型与其各自的分泌产物胰岛素、胰高血糖素、生长抑素和胰多肽之间存在复杂的相互关系。已知这些激素会与不同的胰岛细胞相互作用并调节其功能。胰岛素在体内和体外均抑制A细胞分泌胰高血糖素,在胰岛素缺乏的状态下,会观察到高胰高血糖素水平,而补充胰岛素后该水平会恢复正常。为了确定胰岛素是否也调节胰高血糖素的生物合成,我们研究了其对胰高血糖素基因表达的影响。我们的研究表明,胰岛素以剂量依赖的方式降低克隆仓鼠胰岛细胞系In-R1-G9中胰高血糖素mRNA的稳态水平;通过转录延伸分析评估,这种降低是由于胰高血糖素基因转录受到抑制所致,并且不涉及mRNA稳定性的可检测变化。胰高血糖素基因转录的抑制伴随着细胞提取物和培养基中胰高血糖素免疫反应性的相应降低。我们得出结论,胰岛素不仅可能调节胰高血糖素的分泌,还可能调节胰高血糖素的基因表达。