中华内分泌代谢杂志
中華內分泌代謝雜誌
중화내분비대사잡지
CHINESE JOURNAL OF ENDOCRINOLOGY AND METABOLISM
2011年
4期
328-331
,共4页
林宁%万晓玉%陈雪茹%苏青%董艳
林寧%萬曉玉%陳雪茹%囌青%董豔
림저%만효옥%진설여%소청%동염
糖化终末产物,晚期%氧化应激%基质金属蛋白酶2
糖化終末產物,晚期%氧化應激%基質金屬蛋白酶2
당화종말산물,만기%양화응격%기질금속단백매2
Glycation end-products,advanced%Oxidative stress%Matrix metalloproteinase 2
目的 探讨糖化终末产物(AGEs)对大鼠胰岛细胞株INS-1基质金属蛋白酶2(MMP-2)表达量的影响.方法 培养INS-1细胞,检测MMP-2表达;制备糖化胎牛血清,通过流式细胞仪检测细胞内活性氧簇(ROS)水平,通过逆转录PCR、实时定量PCR和Western印迹方法观察细胞中MMP-2表达量的变化.结果 INS-1细胞中存在MMP-2的表达;AGEs刺激后ROS明显升高(P<0.05),刺激组细胞内MMP-2mRNA表达量和蛋白表达水平均显著高于对照组(P<0.05).结论 提示胰岛β细胞内存在MMP-2表达,AGEs可诱导β细胞MMP-2表达量增高,MMP-2在介导胰岛氧化应激损伤中可能起着重要作用.
目的 探討糖化終末產物(AGEs)對大鼠胰島細胞株INS-1基質金屬蛋白酶2(MMP-2)錶達量的影響.方法 培養INS-1細胞,檢測MMP-2錶達;製備糖化胎牛血清,通過流式細胞儀檢測細胞內活性氧簇(ROS)水平,通過逆轉錄PCR、實時定量PCR和Western印跡方法觀察細胞中MMP-2錶達量的變化.結果 INS-1細胞中存在MMP-2的錶達;AGEs刺激後ROS明顯升高(P<0.05),刺激組細胞內MMP-2mRNA錶達量和蛋白錶達水平均顯著高于對照組(P<0.05).結論 提示胰島β細胞內存在MMP-2錶達,AGEs可誘導β細胞MMP-2錶達量增高,MMP-2在介導胰島氧化應激損傷中可能起著重要作用.
목적 탐토당화종말산물(AGEs)대대서이도세포주INS-1기질금속단백매2(MMP-2)표체량적영향.방법 배양INS-1세포,검측MMP-2표체;제비당화태우혈청,통과류식세포의검측세포내활성양족(ROS)수평,통과역전록PCR、실시정량PCR화Western인적방법관찰세포중MMP-2표체량적변화.결과 INS-1세포중존재MMP-2적표체;AGEs자격후ROS명현승고(P<0.05),자격조세포내MMP-2mRNA표체량화단백표체수평균현저고우대조조(P<0.05).결론 제시이도β세포내존재MMP-2표체,AGEs가유도β세포MMP-2표체량증고,MMP-2재개도이도양화응격손상중가능기착중요작용.
Objective To explore the impact of advanced glycation end-products ( AGEs) on matrix metalloproteinase 2 ( MMP-2) expression in cultivated INS-1 cells. Method INS-1 cells were cultivated and MMP-2 expression was analyzed. Glycated serum was prepared for incubating with INS-1 cell. Reactive oxygen species (ROS) was detected by flow cytometry. The intracelluar MMP-2 expression was analyzed by RT-PCR, realtime PCR and Western blot. The MMP-2 cDNA was expressed in cultivated INS-1 cells. Result The level of ROS treated with AGEs was significantly higher than that in the control( P<0.05 ) , and the levels of MMP-2 and its protein expressions turned out as well( P<0. 05). Conclusion The results suggest that MMP-2 was expressed in INS-1 cells. Increased MMP-2 expression in ?cells may be induced by AGEs, suggesting that MMP-2 might play an important role in oxidative stress-mediated islet injury.