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主动脉夹层动脉瘤中纤溶基因与基质金属蛋白酶-9的表达模式

Patterns of expression of fibrinolytic genes and matrix metalloproteinase-9 in dissecting aortic aneurysms.

作者信息

Schneiderman J, Bordin G M, Adar R, Smolinsky A, Seiffert D, Engelberg I, Dilley R B, Thinnes T, Loskutoff D J

机构信息

Department of General and Vascular Surgery, Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Am J Pathol. 1998 Mar;152(3):703-10.

Abstract

Although extensive tissue remodeling occurs during the various phases of aortic dissection, the underlying proteinases remain to be identified. Matrix metalloproteinase-9 (MMP-9) and components of the fibrinolytic system have been implicated in numerous tissue remodeling events and were therefore analyzed in surgical specimens of acute (n = 9), subacute (n = 4), and chronic (n = 7) aortic dissection by in situ hybridization. In the acute phase, intense plasminogen activator inhibitor 1 (PAI-1) gene expression was apparent in areas interfacing the dissecting hematoma, but no tissue-type PA (t-PA), urokinase-type PA (u-PA), or MMP-9 mRNAs were detected. Although PAI-1 mRNA was still present in the subacute phase, t-PA, u-PA, and MMP-9 mRNAs were now obvious, with PA gene expression co-localizing with areas of PAI-1 gene expression. In the chronic phase, PAI-1 mRNA was demonstrated around erythrocyte extravasations and surrounding bands of medial degeneration. However, there was little expression of PAs in these areas, and no MMP-9 was detected. Thus, fibrinolytic genes and MMP-9 are differentially expressed during the progression of aortic dissections. The kinetics of expression are consistent with acute fibrinolytic shutdown in response to the initial injury, a secondary subacute phase with active proteolysis, and finally, a chronic hypofibrinolytic state. Extensive neovascularization in the chronic phase may further reduce the physical stability of the dissected wall.

摘要

尽管在主动脉夹层的各个阶段都会发生广泛的组织重塑,但其潜在的蛋白酶仍有待确定。基质金属蛋白酶-9(MMP-9)和纤维蛋白溶解系统的成分参与了众多组织重塑事件,因此通过原位杂交技术对急性(n = 9)、亚急性(n = 4)和慢性(n = 7)主动脉夹层的手术标本进行了分析。在急性期,纤溶酶原激活物抑制剂1(PAI-1)基因在与夹层血肿相邻的区域有明显的强烈表达,但未检测到组织型纤溶酶原激活物(t-PA)、尿激酶型纤溶酶原激活物(u-PA)或MMP-9的mRNA。虽然PAI-1 mRNA在亚急性期仍然存在,但此时t-PA、u-PA和MMP-9的mRNA明显可见,PA基因表达与PAI-1基因表达区域共定位。在慢性期,PAI-1 mRNA在红细胞外渗周围和中膜退变的周边带被证实。然而,这些区域PA的表达很少,且未检测到MMP-9。因此,在主动脉夹层进展过程中,纤维蛋白溶解基因和MMP-9的表达存在差异。其表达动力学与对初始损伤的急性纤维蛋白溶解关闭、伴有活性蛋白水解的继发性亚急性期以及最终的慢性低纤维蛋白溶解状态一致。慢性期广泛的新生血管形成可能会进一步降低夹层壁的物理稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b43f/1858402/8c6661b5323e/amjpathol00015-0084-a.jpg

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