Schmidt Gunther, Sirois Francine, Anini Younes, Kauri Lisa M, Gyamera-Acheampong Charles, Fleck Eckart, Scott Fraser W, Chrétien Michel, Mbikay Majambu
Diseases of Aging Program, Ottawa Health Research Institute, Ottawa Hospital, University of Ottawa, Ontario, Canada.
Diabetes. 2006 Feb;55(2):452-9. doi: 10.2337/diabetes.55.02.06.db05-0733.
C57BL/6 (B6) mice develop glucose intolerance with age, whereas C3H/He (C3H) mice do not. In this study, we examined whether this differential glucose homeostasis was associated with differences of proteolytic activation of pancreatic prohormones. Radioimmunoassays showed comparable levels of fasting plasma insulin between the two strains but a significantly lower glucagon level in B6 mice. Pulse-chase analysis of glucagon biosynthesis in isolated pancreatic islets revealed that proglucagon was less efficiently processed in B6 mice. Because proprotein convertase (PC)2 and its 7B2 helper protein are required for this processing, we quantified islet mRNA levels by RT-PCR and protein levels by immunoblotting. The levels of proPC2 mRNA were similar between the two strains, but B6 protein extracts contained less of the mature PC2. In contrast, 7B2 mRNA and protein levels were both significantly lower in B6 pancreas. Sequencing of the 7B2 gene promoter and cDNA in the two strains revealed seven single nucleotide polymorphisms and one dinucleotide insertion/deletion in the cDNA as well as a single nucleotide polymorphism and two insertions/deletions in the promoter. Differential expression of 7B2 may contribute to the difference between B6 and C3H mice not only in glucagon production and secretion but also in glucose tolerance.
C57BL/6(B6)小鼠会随着年龄增长出现葡萄糖不耐受,而C3H/He(C3H)小鼠则不会。在本研究中,我们探究了这种葡萄糖稳态差异是否与胰腺激素原的蛋白水解激活差异有关。放射免疫分析显示,两品系小鼠的空腹血浆胰岛素水平相当,但B6小鼠的胰高血糖素水平显著较低。对分离的胰岛中胰高血糖素生物合成进行脉冲追踪分析发现,B6小鼠中胰高血糖素原的加工效率较低。由于这种加工过程需要前蛋白转化酶(PC)2及其7B2辅助蛋白,我们通过逆转录聚合酶链反应(RT-PCR)对胰岛mRNA水平进行定量,并通过免疫印迹法对蛋白水平进行定量。两品系小鼠的前PC2 mRNA水平相似,但B6蛋白提取物中成熟PC2的含量较少。相比之下,B6胰腺中7B2的mRNA和蛋白水平均显著较低。对两品系小鼠7B2基因启动子和cDNA进行测序,发现在cDNA中有7个单核苷酸多态性和1个二核苷酸插入/缺失,在启动子中有1个单核苷酸多态性和2个插入/缺失。7B2的差异表达可能不仅导致B6和C3H小鼠在胰高血糖素产生和分泌方面存在差异,还导致它们在葡萄糖耐量方面存在差异。