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作 者:王瑞涛[1] 宋科瑛[1] 施杰毅 卢列盛[1] 杨静[2] 王庆萍[2] 李克[1]
机构地区:[1]上海交通大学附属第一人民医院普外科,200080 [2]上海市长宁区中心医院病理科
出 处:《中华医学杂志》2009年第20期1426-1429,共4页National Medical Journal of China
基 金:国家教育部留学回国人员启动基金;上海市科学技术委员会启明星基金(05QMX1440);上海交通大学优秀青年教师基金
摘 要:目的探讨Ca^2+-非依赖性磷酸脂酶A2(iPLA2)在人胰岛的表达及在胰岛素分泌功能中的作用。方法正常人胰腺组织切片免疫组织化学染色及人胰岛Western印迹方法检测,观察iPLA2在人胰岛中的表达情况;随机分组对照研究iPLA2选择性抑制剂溴烯醇内酯(BEL)对离体人胰岛的葡萄糖刺激引起胰岛素分泌反应的影响。结果在人胰岛iPLA2高表达,与抗胰岛素染色分布一致,而外分泌腺很少表达;与对照组相比,BEL处理组胰岛素分泌反应明显减弱[(0.8285±0.0803)ng·胰岛^-1·h^-1,P〈0.01],BEL通过抑制iPLA2活性抑制了葡萄糖刺激引起的离体人胰岛胰岛素分泌。结论iPLA2在人胰岛β细胞高表达并在葡萄糖刺激胰岛β细胞胰岛素分泌过程起到重要的作用。Objective To assess the role of calcium-independent phospholipase A2 ( iPLA2 ) in human pancreatic islets. Methods The immunohistochemical analysis and Western blot were employed to examine iPLA2 expression in human pancreatic islets. Bromoenol lactone ( BEL), a selective inhibitor of iPLA2, was used in a randomized controlled trial to compare its influence to glucose-stimulated insulin secretion. Results iPLA2 was expressed predominantly in islet ceils co-stained by insulin but was barely detected in the exocrine acinar cells. Western blot results indicated that islet cells expressed an iPLA2- immunoreactive band at the 80 000 region. Glucose-stimulated insulin secretory response was dramatically reduced in islets pretreated with BEL (0. 8285 ± 0. 0803 ng· islet- 1· h - 1 ) as compared with the control ( 1. 2264 ±0. 0568 ng · islet^-1· h^-1 ) (p 〈0. 01 ). BEL inhibited glucose stimulated insulin secretion from isolated human islets. Conclusion iPLA2 signaling plays an important role in glucose-stimulated insulin secretion under the physiological conditions.
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