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融合蛋白HSP65-6×P277在NOD鼠中降糖作用的机制研究(英文)

Study on the hypoglycemic mechanism of the fusion protein HSP65-6×P277 in NOD mice

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【作者】 金亮; 王宇; 朱爱华; 刘景晶;

【Author】 JIN Liang1,WANG Yu1,ZHU Ai-hua2,LIU Jing-jing11Minigene Pharmacy Laboratory,School of Life Science & Technology,China Pharmaceutical University,Nanjing 210009,Jiangsu,China;2Key Laboratory of Biotechnology for Medicinal Plants of Jiangsu Province,Xuzhou Normal University,Shanghai Road,Xuzhou 221116,Jiangsu,China

【机构】 中国药科大学生命科学与技术学院; 徐州师范大学江苏省植物药物生物技术重点实验室;

【摘要】 目的:探讨融合蛋白HSP65 -6×P277在NOD鼠中的降糖作用机制。方法:融合蛋白HSP65 -6×P277通过鼻腔给药方式,在不添加任何佐剂的情况下3次免疫4周龄雌性NOD小鼠。观察该融合蛋白对NOD小鼠血糖,细胞因子水平,抗体类型和胰腺炎严重程度的影响。结果:融合蛋白HSP65 -6×P277免疫组动物血清中含有高水平的IL-4和低水平的IL-2 ,P277特异性抗体类型主要为IgGl和IgG2b,IgG2a水平较低;T细胞增殖实验的培养上清中含有较高水平的IL-10和较低水平的IFN-γ;胰腺炎的严重程度和1型糖尿病的发病率显著降低。结论:诱导了Th2免疫反应可能是HSP65-6×P277预防1型糖尿病发生的作用机制之一。

【Abstract】 AIM:To evaluate the hypoglycemic mechanism of the fusion protein HSP65-6×P277 in NOD mice.METHODS:The fusion protein was used to immunize 4-week old female NOD mice with three i.n.inoculations in the absence of adjuvants.The effects of HSP65-6×P277 on NOD mice were investigated by observing the change of blood glucose,cytokine levels,antibody types and degree of insulitis.RESULTS:The sera collected from HSP65-6×P277 treated mice,contained relatively high levels of interleukin IL-4 but low levels of IL-2,and the antibody types were almost exclusively of the IgGl and IgG2b subclass,but at very low levels of IgG2a.T cells from HSP65-6×P277 treated mice when incubated with HSP-peptide conjugate showed an increase in IL-10 secretion and a decrease in interferon (IFN)-γ secretion.HSP65-6×P277 treatment reduced insulitis and T1DM incidence.CONCLUSION:The hypoglycemic mechanism of the fusion protein HSP65-6×P277 is related to its inducing Th2 responses.

【关键词】 热休克蛋白65; p277肽; Th1/Th2细胞; 细胞因子;
【Key words】 heat shock protein 65; P277; Th1/Th2 cells; cytokines;
【基金】 supported by China National Natural Science Fund Commit-tee(Grant No.30701023,30672464 and 30500458)
  • 【文献出处】 中国临床药理学与治疗学 ,Chinese Journal of Clinical Pharmacology and Therapeutics , 编辑部邮箱 ,2009年10期
  • 【分类号】R587.1
  • 【下载频次】112
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