CORONARY-ARTERY ULTRASTRUCTURAL-CHANGES IN CARDIAC TRANSPLANT ATHEROSCLEROSIS IN THE RABBIT

被引:41
作者
KUWAHARA, M
JACOBSSON, J
KUWAHARA, M
KAGAN, E
RAMWELL, PW
FOEGH, ML
机构
[1] GEORGETOWN UNIV,MED CTR,DEPT SURG,DIV CARDIOVASC SURG,4 S HOSP 4402,3800 RESERVOIR RD NW,WASHINGTON,DC 20007
[2] GEORGETOWN UNIV,MED CTR,DEPT PATHOL,WASHINGTON,DC 20007
[3] GEORGETOWN UNIV,MED CTR,DEPT PHYSIOL & BIOPHYS,WASHINGTON,DC 20007
关键词
D O I
10.1097/00007890-199111000-00001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Accelerated coronary atherosclerosis is the limiting factor for long-term survival of cardiac transplant recipients, but its pathogenesis is poorly understood. Morphologic and ultrastructural changes in suitable models may help explain the underlying mechanisms. In this study, early (3, 7, 14, and 21 days) and late (42 days) ultrastructural changes of the coronary artery were characterized in rabbit cardiac allografts. Thirty-four New Zealand white male rabbits (3.0-4.0 kg) served as donors and recipients. All recipients received cyclosporine (10 mg/kg/day i.m.) as immunosuppressant. In order to increase the normally very low cholesterol levels in rabbits, both the donor and recipient animals were fed a 0.5% cholesterol diet. Recipient animals were sacrificed between 3 days and 6 weeks after transplantation. The specimens from both donor and recipient were examined by transmission electron microscopy, immunohistochemistry, and morphometry. Our data indicate that intimal thickening was initiated with smooth muscle cell migration within 1 week after transplantation, and occurrence of macrophage-derived foam cells and vacuolized smooth muscle cells 3 weeks after transplantation. These changes occurred in the presence of an ultrastructurally intact endothelium. Platelets were only seldom seen adhering to the endothelium. In contrast, lymphocytes and monocytes were frequently found adhering to the endothelium at 2 and 3 weeks posttransplantation. From 3 weeks posttransplantation, lymphocytes were seen only occasionally in the intima but not in the media. This study suggests that early events elicit a change in the smooth muscle cells in the media to the secretory phenotype that migrates to the intima and proliferate. Lymphocyte and monocyte adhesion to the endothelium may enhance smooth muscle migration and proliferation. The large macrophage involvement may relate to the high serum cholesterol levels induced by the cholesterol diet. All these changes occurred in the presence of a structurally normal endothelium and without apparent platelet involvement.
引用
收藏
页码:759 / 765
页数:7
相关论文
共 23 条
[1]  
ALONSO DR, 1977, AM J PATHOL, V87, P415
[2]  
ASOTRA S, 1989, TRANSPLANT P, V21, P3695
[3]  
Barnhart G R, 1987, Transplant Rev (Orlando), V1, P31
[4]  
BILLINGHAM ME, 1987, TRANSPLANT P, V19, P19
[5]   RECENT ADVANCES IN MOLECULAR PATHOLOGY - SMOOTH-MUSCLE PHENOTYPIC CHANGES IN ARTERIAL-WALL HOMEOSTASIS - IMPLICATIONS FOR THE PATHOGENESIS OF ATHEROSCLEROSIS [J].
CAMPBELL, GR ;
CAMPBELL, JH .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1985, 42 (02) :139-162
[6]   SIGNIFICANCE OF QUIESCENT SMOOTH-MUSCLE MIGRATION IN THE INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
SCHWARTZ, SM .
CIRCULATION RESEARCH, 1985, 56 (01) :139-145
[7]  
FERNS G, 1990, AM J PATHOL, V137, P403
[8]   INHIBITION OF CORONARY-ARTERY TRANSPLANT ATHEROSCLEROSIS IN RABBITS WITH ANGIOPEPTIN, AN OCTAPEPTIDE [J].
FOEGH, ML ;
KHIRABADI, BS ;
CHAMBERS, E ;
AMAMOO, S ;
RAMWELL, PW .
ATHEROSCLEROSIS, 1989, 78 (2-3) :229-236
[9]  
FOEGH ML, 1987, TRANSPLANT P, V19, P90
[10]  
JORIS I, 1983, AM J PATHOL, V113, P341