Evidence for the rapid onset of apoptosis in medial smooth muscle cells after balloon injury

被引:45
作者
Perlman, H
Maillard, L
Krasinski, K
Walsh, K
机构
[1] TUFTS UNIV,QUEEN ELIZABETH MED CTR,DIV CARDIOVASC RES,SCH MED,BOSTON,MA 02135
[2] TUFTS UNIV,SACKLER SCH BIOMED SCI,PROGRAM CELL MOL & DEV BIOL,BOSTON,MA 02111
关键词
balloon; apoptosis; angioplasty; muscle; smooth; remodeling;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background Vascular myocyte apoptotic cell death has been reported in human atherectomy and endarterectomy specimens and for neointimal smooth muscle cells (SMCs) in balloon-injured rat carotid arteries between 7 and 30 days after injury. However, the immediate effect of balloon injury on medial SMC viability has not been examined. Methods and Results Rat carotid arteries were harvested at the time of balloon injury (T=0) and at 0.5, 1, 2, and 4 hours after injury. Uninjured Vessels or Vessels harvested at the time of injury (T=0) did not display evidence of apoptosis. However, as early as 30 minutes after injury, 70% of medial SMCs appeared apoptotic by TdT-mediated dUTP nick end labeling (TUNEL) analysis and by the appearance of condensed chromatin. High frequencies of TUNEL-positive cells were also observed at 1 and 2 hours after injury but not at 4 hours. Transmission electron microscopy revealed many cells with morphological characteristics of apoptosis in the injured sections. A marked decrease in bcl-X expression was detected in the most luminal layers of the media To corroborate these findings in a second animal model, rabbit external iliac arteries were analyzed after balloon angioplasty. Apoptotic cell death was evident in rabbit arteries at 30 minutes and at 4 hours after injuIy. Conclusions As early as 30 minutes after balloon injury, myocytes appear to undergo apoptotic cell death at a high frequency as shown by TUNEL staining, chromatin condensation, and the appearance of morphological features in electron micrographs. The induction of apoptosis coincides with a marked down regulation of bcl-X expression.
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收藏
页码:981 / 987
页数:7
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