Zheng Yun-cheng
Yao Xue Xue Bao. 2015 Dec;50(12):1668-72.
GLP-1 has a variety of anti-diabetic effects. However, native GLP-1 is not suitable for treatment of diabetes due to its short half-life (t½, 2-5 min). Exendin-4 is a polypeptide isolated from lizard saliva, which can bind to GLP-1 receptor, produce physiological effects similar to GLP-1, t½ up to 2.5 h, therefore, we developed a long-lasting GLP-1 receptor agonists and GLP-1-exendin-4 fusion IgG4 Fc [GLP-1-exendin-4/ IgG4(Fc)]. We constructed the eukaryotic expression vector of human GLP-1-exendin-4/IgG4(Fc)-pOptiVEC- TOPO by gene recombination technique and expressed the fusion protein human GLP-1-IgG4 (Fc) in CHO/DG44 cells. The fusion protein stimulated the INS-1 cells secretion of insulin, GLP-1, exendin-4 and fusion protein in CD1 mice pharmacokinetic experiments, as well as GLP-1, exendin-4 and fusion protein did anti-diabetic effect on streptozotocin induced mice. Results demonstrated that the GLP-1-exendin-4/IgG4(Fc) positive CHO/DG44 clones were chosen and the media from these positive clones. Western blotting showed that one protein band was found to match well with the predicted relative molecular mass of human GLP-1-exendin-4/IgG4(Fc). Insulin RIA showed that GLP-1-exendin-4/IgG4(Fc) dose-dependently stimulated insulin secretion from INS-1 cells. Pharmacokinetic studies in CD1 mice showed that with intraperitoneal injection (ip), the fusion protein peaked at 30 min in circulation and maintained a plateau for 200 h. Natural biological half-life of exendin-4 was (1.39 ± 0.28) h, GLP-1 in vivo t½ 4 min, indicating that fusion protein has long-lasting effects on the modulation of glucose homeostasis. GLP-1-exendin-4/IgG4(Fc) was found to be effective in reducing the incidence of diabetes in multiple-low-dose streptozotocin-induced diabetes in mice, longer duration of the biological activity of the fusion protein. The biological activity was significantly higher than that of GLP-1 and exendin-4. GLP-1-exendin-4/IgG4(Fc) has good anti-diabetic activity. It can be used as a long-acting GLP-1 agonists.
胰高血糖素样肽-1(GLP-1)具有多种抗糖尿病作用。然而,天然GLP-1因其半衰期短(t½,2 - 5分钟)而不适合用于糖尿病治疗。艾塞那肽-4是从蜥蜴唾液中分离出的一种多肽,它能与GLP-1受体结合,产生与GLP-1相似的生理效应,半衰期长达2.5小时。因此,我们开发了一种长效GLP-1受体激动剂和GLP-1 - 艾塞那肽-4融合IgG4 Fc[GLP-1 - 艾塞那肽-4/IgG4(Fc)]。我们通过基因重组技术构建了人GLP-1 - 艾塞那肽-4/IgG4(Fc)-pOptiVEC-TOPO真核表达载体,并在CHO/DG44细胞中表达了融合蛋白人GLP-1 - IgG4(Fc)。在CD1小鼠药代动力学实验中,融合蛋白刺激了INS-1细胞分泌胰岛素、GLP-1、艾塞那肽-4,并且GLP-1、艾塞那肽-4和融合蛋白对链脲佐菌素诱导的小鼠具有抗糖尿病作用。结果表明,选择了GLP-1 - 艾塞那肽-4/IgG4(Fc)阳性的CHO/DG44克隆及其培养基。蛋白质印迹法显示,发现一条蛋白带与预测的人GLP-1 - 艾塞那肽-4/IgG4(Fc)相对分子质量匹配良好。胰岛素放射免疫分析表明,GLP-1 - 艾塞那肽-4/IgG4(Fc)剂量依赖性地刺激INS-1细胞分泌胰岛素。在CD1小鼠中的药代动力学研究表明,腹腔注射(ip)后融合蛋白在循环中30分钟达到峰值,并维持平台期200小时。艾塞那肽-4的天然生物半衰期为(1.39 ± 0.28)小时,GLP-1在体内的t½为4分钟,表明融合蛋白对葡萄糖稳态调节具有长效作用。发现GLP-1 - 艾塞那肽-4/IgG4(Fc)可有效降低多次低剂量链脲佐菌素诱导的小鼠糖尿病发病率,融合蛋白的生物活性持续时间更长。其生物活性显著高于GLP-1和艾塞那肽-4。GLP-1 - 艾塞那肽-4/IgG4(Fc)具有良好的抗糖尿病活性。它可作为一种长效GLP-1激动剂。