Carotid plaque instability and ischemic symptoms are linked to immaturity of microvessels within plaques

被引:189
作者
Dunmore, Benjamin J.
McCarthy, Mark J.
Naylor, A. Ross
Brindle, Nicholas P. J.
机构
[1] Univ Leicester, Dept Cardiovasc Sci, Vasc Surg Grp, Leicester LE2 7LX, Leics, England
[2] Univ Cambridge, Dept Obstet & Gynaecol, Cambridge CB2 1TN, England
关键词
D O I
10.1016/j.jvs.2006.08.072
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Instability and rupture of carotid atherosclerotic plaques leads to thromboemboli and ischemic symptoms. Angiogenesis occurs within atherosclerotic plaques, and plaque vulnerability and symptomatic carotid disease have been associated with increased numbers of microvessels. In addition to microvessel number, it is possible that the phenotypes of intraplaque vessels could influence plaque stability. To test this, the morphology and maturity of vessels within plaques from symptomatic and asymptomatic patients was determined. Methods: Carotid plaques were collected after endarterectomy from a cohort of 13 asymptomatic patients and 30 symptomatic patients. Plaques were sectioned and immunostained for the presence of endothelial cells, vascular smooth muscle cells, macrophages, and vascular endothelial growth factor. Sections were assessed for microvessel morphology, maturity as judged by smooth muscle cell cover, and the presence of vascular endothelial growth factor and macrophages. Results: Two types of vascular structure were observed within plaques, microvessels and dilated, highly irregular multilobular vessels. These irregular dysmorphic vessels were found almost exclusively in plaques from symptomatic patients. The dysmorphic vessels lacked smooth muscle cells and were highly immature. Plaques also contained vascular endothelial growth factor, and this was observed adjacent to the dysmorphic vessels. This growth factor was found colocalized with macrophages. Conclusions. Symptomatic carotid plaques contain abnormal, immature microvessels similar to those found in tumors and healing wounds. Such vessels could contribute to plaque instability by acting as sites of vascular leakage by inflammatory cell recruitment. The immature vessels within plaques may be therapeutic targets for promoting plaque stabilization.
引用
收藏
页码:155 / 159
页数:5
相关论文
共 30 条
[21]   Inhibition of plaque neovascularization reduces macrophage accumulation and progression of advanced atherosclerosis [J].
Moulton, KS ;
Vakili, K ;
Zurakowski, D ;
Soliman, M ;
Butterfield, C ;
Sylvin, E ;
Lo, KM ;
Gillies, S ;
Javaherian, K ;
Folkman, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) :4736-4741
[22]  
OBRIEN ER, 1994, AM J PATHOL, V145, P883
[23]  
PAKU S, 1991, LAB INVEST, V65, P334
[24]   Heterogeneity of the angiogenic response induced in different normal adult tissues by vascular permeability factor/vascular endothelial growth factor [J].
Pettersson, A ;
Nagy, JA ;
Brown, LF ;
Sundberg, C ;
Morgan, E ;
Jungles, S ;
Carter, R ;
Krieger, JE ;
Manseau, EJ ;
Harvey, VS ;
Eckelhoefer, IA ;
Feng, D ;
Dvorak, AM ;
Mulligan, RC ;
Dvorak, HF .
LABORATORY INVESTIGATION, 2000, 80 (01) :99-115
[25]   Morphological characteristics of the microvasculature in healing myocardial infarcts [J].
Ren, GF ;
Michael, LH ;
Entman, ML ;
Frangogiannis, NG .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2002, 50 (01) :71-79
[26]   Patterns of brain angiogenesis after vascular endothelial growth factor administration in vitro and in vivo [J].
Rosenstein, JM ;
Mani, N ;
Silverman, WF ;
Krum, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :7086-7091
[27]   PLAQUE ULCERATION AND LUMEN THROMBUS ARE THE MAIN SOURCES OF CEREBRAL MICROEMBOLI IN HIGH-GRADE INTERNAL CAROTID-ARTERY STENOSIS [J].
SITZER, M ;
MULLER, W ;
SIEBLER, M ;
HORT, W ;
KNIEMEYER, HW ;
JANCKE, L ;
STEINMETZ, H .
STROKE, 1995, 26 (07) :1231-1233
[28]  
TAYLOR DW, 1991, NEW ENGL J MED, V325, P445
[29]   Atherosclerotic plaque progression and vulnerability to rupture - Angiogenesis as a source of intraplaque hemorrhage [J].
Virmani, R ;
Kolodgie, FD ;
Burke, AP ;
Finn, AV ;
Gold, HK ;
Tulenko, TN ;
Wrenn, SP ;
Narula, J .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2054-2061
[30]  
ZHANG Y, 1993, AM J PATHOL, V143, P164