Direct evidence for the importance of p130 in injury response and arterial remodeling following carotid artery ligation

被引:17
作者
Sindermann, JR
Smith, J
Köbbert, C
Plenz, G
Skaletz-Rorowski, A
Solomon, JL
Fan, L
March, KL
机构
[1] Univ Munster, Inst Arteriosclerosis Res, D-48149 Munster, Germany
[2] Univ Munster, Dept Med, D-48149 Munster, Germany
[3] Indiana Univ, Med Ctr, Krannert Inst Cardiol, Indianapolis, IN 46202 USA
[4] Indiana Univ, Med Ctr, Indiana Ctr Vasc Biol & Med, Indianapolis, IN 46202 USA
关键词
arteries; gene expression; remodeling; restenosis; smooth muscle;
D O I
10.1016/S0008-6363(02)00272-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Remodeling of arterial morphology in atherosclerosis, hypertension, and restenosis following angioplasty involves controlled alterations in total vascular circumference which critically modulate sequelae Of change, in vessel wall mass. Despite the clinical relevance of this process little is known about the pathophysiology, especially the correlation between smooth muscle cell proliferation and remodeling. Methods: Carotid artery ligation was applied to mice with targeted disruption of the p130 gene (p130 -/-). Mice were allowed to recover for 3 weeks after ligation and then perfusion fixed for histologic and morphometric analysis, Results: P130 -/- mice were indistinguishable from control littermates concerning, size and As for the aorta, carotid arteries and femoral arteries, no significant difference,, were found between the groups with regard to vessel size and cellular density of the vessel wall of non-instrumented vessels. In contrast. following carotid artery ligation we found p130 -/- mice (n = 8) to develop a significant increase in vessel wall area compared to controls (n = 9). Mean values ranged from 3.07 x 10(-2) +/- 0.20 x 10(-2) -3.56 x 10(-2) +/- 0.62 x 10(-2) mm(2) for p130 -/- mice versus 2.26 x 10(-2) +/- 0.13 x 10(-2) -2.57 x 10(-2) +/- 0.26 x 10(-2) mm(2) for controls (p = 0.02) along the lesion studied. This increase in vessel wall area was primarily due to a sevenfold mean increase in neointima in p130 -/- mice yielding mean values of 0.43+/-0.18 - 1.19+/-0.70 x 10(-2) mm(2). Remarkably, despite vessel all increase. the lumen area v as not statistically different for both groups. Conclusions: The data indicate that the toss of the cell cycle inhibitor p130 leads to an enhanced injury response, implicating a central rote of p130 in cell cycle control during response to injury in the vessel wall. The enhanced injury response in the context of p130 preserves the ability to perform perfect remodeling. thus the remodeling, capacity is preserved even in the context of this injury model. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:676 / 683
页数:8
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