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膜型基质金属蛋白酶表达促进大鼠血管内膜SMC迁移的研究

Overexpression of Membrane Type Matrix Metalloproteinase in Neointima Facilitate Smooth Muscle Cells Migration During Vascular Intimal Hyperplasia in Rats

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【作者】 李济宇余波张延龄翟为溶

【Author】 LI Ji-yu, YU Bo, ZHANG Yan-ling, et al( Department of Surgery, Xinhua Hospital, Shanghai 200092 , China )

【机构】 上海第二医科大学新华医院外科复旦大学华山医院外科复旦大学病理教研室 上海 200092

【摘要】 目的探讨血管内膜增生(IH)过程中膜型基质金属蛋白酶(MT-MMP)mRNA的表达与平滑肌细胞(SMC)迁移的关系。 方法建立大鼠血管IH模型,以原位杂交法检测术后血管壁中MT-MMP mRNA的表达,并以特殊染色及Desmin免疫组化法对SMC进行半定量测定,观察两者的相关性。 结果IH过程中,MT-MMP mRNA与Desmin表达之间存在一定的相关性。术后前4周呈正相关(r=0.933,P<0.05),而此后表现为负相关(r=-0.42,P=NS)。 结论IH早期(术后1月),MT-MMP mRNA过度表达,激活MMPs,介导SMC由中膜向内膜迁移。

【Abstract】 Objective To explore the relationship between the mRNA expression of membrane type matrix metalloproteinase ( MT - MMP) , an activator of matrix metalloproteinases zymogen (pro - MMPs) , and smooth muscle cells ( SMC) migration in the development of vascular intimal hyperplasia ( IH ). Methods We established a model of rat autologous vein graft in the carotid artery, and investigated the expression of MT - MMP mRNA using ire situ hybridization. SMC was measured using special staining and im-munohistochemical assays. Results Positive correlation was found between the expression of MT - MMP mRNA and SMC migration during the first four weeks of IH (r = 0. 933, P <0. 05) , while negative correlation was found in the rest time of IH ( r = -0. 42, P = NS). Conclusion We suggest that in the early stage of IH , MT - MMP mRNA overexpresses and causes degradation of extracellular matrix ( ECM ) by activating pro -MMPs, which eventually enable the medial SMC migrate to the intima.

【关键词】 内膜增生MT-MMP mRNA平滑肌细胞大鼠
【Key words】 intimal hyperplasiaMT-MMP mRNAsmooth muscle cellsrat
  • 【文献出处】 上海第二医科大学学报 ,Acta Universitatis Medicinalis Secondae Shanghai , 编辑部邮箱 ,2003年01期
  • 【分类号】R654.4
  • 【被引频次】5
  • 【下载频次】71
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