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基质金属蛋白酶3在实验性大鼠腹主动脉瘤模型中的表达
引用本文:赵新,景在平,熊江,江少杰. 基质金属蛋白酶3在实验性大鼠腹主动脉瘤模型中的表达[J]. 第二军医大学学报, 2002, 23(8): 877-879
作者姓名:赵新  景在平  熊江  江少杰
作者单位:第二军医大学长海医院血管外科,全军血管外科研究所,上海,200433
基金项目:军队杰出人才基金资助项目 (98J0 0 5 ),上海市卫生系统百名跨世纪优秀学科带头人培养计划基金(97BR0 4 7),上海市科技发展基金攻关计划项目(0 0 4 4 190 2 9),长海医院学科攀登计划基金资助课题
摘    要:目的:检测基质金属蛋白酶3(MMP-3)在大鼠正常动脉及腹动脉瘤模型组织中的表达,以探讨其在腹主动脉瘤发病机制中的作用。方法:建立大鼠腹主动脉瘤灌注模型,应用免疫组织化学和分子原位杂交技术检测MMP-3的表达。结果:正常动脉壁组织MMP-3蛋白表达为弱阳性或阴性,而动脉瘤组织中MMP-3蛋白表达显著增高,阳性率为8/8/MMP-3阳性染色主要位于中膜的平滑肌细胞和外膜的炎症细胞,其中炎症细胞浸润的区域染色明显增强,MMP-3 mRNA在动脉瘤组织中呈阳性表达,在动脉外膜炎症细胞浸润的区域和小血管聚集区呈强阳性;对照组动脉组织未见MMP-3 mRNA阳性表达。结论:腹主动脉瘤组织中MMP-3蛋白及mRNA较正常动脉组织表达显著增高,尤其在炎症细胞浸润的区域表达明显增强;提示MMP-3可能在腹主动脉瘤发生发展过程中起到关键的起始因子的作用。

关 键 词:基质金属蛋白酶3 大鼠 腹主动脉瘤 免疫组织化学 原位杂交
文章编号:0258-879X(2002)08-0877-03
修稿时间:2002-03-01

Expression of matrix metalloproteinase-3 in experimental abdominal aortic aneurysm rat model
ZHAO Xin,JING Zai Ping,XIONG Jiang,JIANG Shao Jie. Expression of matrix metalloproteinase-3 in experimental abdominal aortic aneurysm rat model[J]. Former Academic Journal of Second Military Medical University, 2002, 23(8): 877-879
Authors:ZHAO Xin  JING Zai Ping  XIONG Jiang  JIANG Shao Jie
Abstract:Objective:To investigate matrix metalloproteinase 3 (MMP 3) expression in experimental abdominal aortic aneurysms (AAA) rat model. Methods:The expression of MMP 3 were observed in 8 rat AAA models and 8 normal control aortic tissues using immunohistochemistry and molecular in situ hybridization technique. Results:The positive rate of MMP 3 protein expression was 8/8 in AAA and it was markedly increased compared with that of control samples( P <0.01). The positive expression of MMP 3 protein, mostly in adventitia inflammatory infiltration areas and media vascular smooth muscle cells in AAA model tissues, was much stronger than that of control aortic tissues. The expression of MMP 3 mRNA in AAA group was much stronger than that in control group. The expression pattern of MMP 3 mRNA in AAA was consistent with expression of MMP 3 protein. Conclusion:The protein and mRNA expression of MMP 3 is markedly increased in experimental AAA than in control abdominal aortic tissues. MMP 3 may be a key initial factor in experimental AAA formation and progression.
Keywords:aortic aneurysm  abdominal  metalloproteinases  immunohistochemistry  in situ hybridization  model  cardiovascular
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