Quoix Nicolas, Cheng-Xue Rui, Guiot Yves, Herrera Pedro L, Henquin Jean-Claude, Gilon Patrick
Unit of Endocrinology and Metabolism UCL 55.30, Faculty of Medicine, Université Catholique de Louvain, Avenue Hippocrate 55, B-1200 Brussels, Belgium.
FEBS Lett. 2007 Sep 4;581(22):4235-40. doi: 10.1016/j.febslet.2007.07.068. Epub 2007 Aug 7.
The control of glucagon secretion by pancreatic alpha-cells is poorly understood, largely because of the difficulty to recognize living alpha-cells. We describe a new mouse model, referred to as GluCre-ROSA26EYFP (or GYY), allowing easy alpha-cell identification because of specific expression of EYFP. GYY mice displayed normal glycemic control during a fasting/refeeding test or intraperitoneal insulin injection. Glucagon secretion by isolated islets was normally inhibited by glucose and stimulated by adrenaline. Ca(2+) responses to arginine, adrenaline, diazoxide and tolbutamide, were similar in GYY and control mice. Hence, this new mouse model is a reliable and powerful tool to specifically study alpha-cells.
胰腺α细胞对胰高血糖素分泌的控制机制目前尚不清楚,主要原因是难以识别活的α细胞。我们描述了一种新的小鼠模型,称为GluCre-ROSA26EYFP(或GYY),由于EYFP的特异性表达,使得α细胞易于识别。在禁食/再喂食试验或腹腔注射胰岛素期间,GYY小鼠的血糖控制正常。分离的胰岛分泌的胰高血糖素通常受到葡萄糖的抑制,并受到肾上腺素的刺激。GYY小鼠和对照小鼠对精氨酸、肾上腺素、二氮嗪和甲苯磺丁脲的Ca(2+)反应相似。因此,这种新的小鼠模型是专门研究α细胞的可靠且强大的工具。