摘要
目的:研究大鼠胰腺发育不同阶段Munc131基因及蛋白表达的变化及Munc131在胰岛素释放过程中的作用方法:应用显微分离及提取技术获得大鼠胚胎发育12.5d(E12.5),E15.5,E18.5,新生大鼠,出生后21d(P21)及成年大鼠胰腺组织;另外,从大鼠胚胎发育15d开始给予孕鼠半量饮食,造成宫内发育迟缓动物模型,提取其新生大鼠胰腺组织.采用RTPCR,RealtimePCR和Westernblot技术确定Munc131的表达情况,并测定不同发育时期血中胰岛素浓度.结果:胰岛素基因从E12.5开始出现,Munc131基因从E15.5开始表达,随着胎龄的增长,二者表达量皆增多.E15.5和E18.5时munc131蛋白表达量较少,以后明显增多.自E18.5即检测到血中胰岛素的存在,随着胚胎的发育,血胰岛素浓度逐渐升高.宫内发育迟缓新生大鼠比正常新生大鼠血胰岛素浓度低,同时Munc131基因及蛋白表达量亦比正常对照组明显减少.结论:Munc131在胰岛素释放过程中的作用,随着胚胎发育期胰岛素分泌的增多表达也增加,宫内发育迟缓新生大鼠胰岛素分泌减少时,Munc131的表达亦减少.
AIM： To investigate the expression of Munc13-1 during various stages of embryonic pancreatic development in rats and define the effect of Munc13-1 on insulin secretion. METHODS： Pancreata of rat embryonic day 12.5 （ El2.5 ）, El5.5, El8.5, new-born, 21 d after birth （P21） and adult rats were dissected under microscope respectively. In addition, the animal models of intrauterine growth retardation （ IUGR ） in rats were made by 50% calorie restriction in pregnant rats from gestational day 15 until term. After abstraction of totle RNA and protein, the techniques of RT-PCR, real-time PCR, Western blot and ELISA were used to study the expression of Munc13-1 and insulin secretion. RESULTS： The genes of insulin and Munc13- 1 began to be expressed from E12.5 and E15.5 respectively and their expressions were increased as the fetus grew. The result of Western blot showed that the expression of Munc13-1 was low at E15.5 and E18.5 and increased later. Blood insulin level was detected at El8.5 and increased rapidly thereafter. The blood insulin level and the expression of Munc13-1 were reduced simultaneously in IUGR models compared with normal newborn rats. CONCLUSION： The expression of Munc13-1 is accordant to blood insulin level and plays an essential role in insulin exocytosis.
出处
《第四军医大学学报》
北大核心
2006年第9期832-834,共3页
Journal of the Fourth Military Medical University
基金
江苏省科委应用基础项目(BK20011119)
