RegIII/胰岛素原双基因质粒的构建及其对1型糖尿病小鼠的治疗作用
Recombination of RegIII-proinsulin-pBudCE4.1 plasmid and its therapeutic effect on STZ-induced type 1 diabetes mellitus
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摘要:
构建含小鼠RegIII和胰岛素原基因的双基因质粒, 观察其对1型糖尿病小鼠的治疗作用, 并初步探 讨其作用机制。采用连续小剂量STZ腹腔注射的方法建立1型糖尿病小鼠模型, 肌内注射给予RegIII/胰岛素原双基因质粒, 治疗4周, 每周给药1次, 动态监测小鼠血糖的变化; 并通过Western blotting、ELISA、MTT、HE病理组织学分析及Tunel检测等方法研究其作用机制。结果表明, 双基因质粒可显著改善1型糖尿病小鼠的高血糖症状 (P < 0.01), 抑制脾淋巴细胞增殖, 恢复1型糖尿病小鼠体内Th1/Th2反应的平衡和胰岛素的正常分泌; HE及Tunel分析表明, 双基因质粒可减少胰岛炎性细胞浸润和胰岛细胞的凋亡。提示RegIII/胰岛素原双基因质粒对1型糖尿病具有明显的治疗作用, 其作用机制与诱导免疫耐受和促进β细胞再生有关。
Abstract:The aim of this study is to investigate the therapeutic effect of RegIII-proinsulin-pBudCE4.1 plasmid on streptozotocin (STZ)-induced type 1 diabetes mellitus and its underlying mechanisms. The model of type 1 diabetes mellitus was established by intraperitoneal injections of STZ (40 mg·kg−1) to Balb/c mice for five consecutive days. Then, ten type 1 diabetic mice were intramuscularly injected with 100 μg RegIII-proinsulin- pBudCE4.1 plasmid for 4 weeks (one time/week) and the blood glucose levels were monitored every week; whereas another ten diabetic mice served as negative control group were injected with pBudCE4.1 vector at the same dose. Normal control and model control mice were treated with normal saline at identical volume under the same way. Western blotting, MTT assay, ELISA, HE staining and Tunel assay were applied to explore the underlying mechanisms. Results showed that RegIII-proinsulin-pBudCE4.1 plasmid ameliorated the hyperglycemia symptoms in diabetic mouse remarkably. It induced an immunological tolerance state in type 1 diabetic mice by inhibiting the proliferation of splenic lymphocytes and recovering Th1/Th2 balance evidenced by MTT and ELISA analysis. Furthermore, it elevated insulin concentration in the serum of type 1 diabetic mice and promoted the regeneration of β cells supported by the results of HE staining and Tunel assay. In conclusion, RegIII-proinsulin-pBudCE4.1 plasmid possesses powerful anti-diabetic ability, which may be involved in the inducing of immunological tolerance and enhancing β cells recovery.
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