Negligible contribution of coronary adventitial fibroblasts to neointimal formation following balloon angioplasty in swine

被引:13
作者
Fleenor, Bradley S. [1 ,2 ]
Bowles, Douglas K. [1 ,2 ,3 ,4 ]
机构
[1] Univ Missouri, Dept Biomed Sci, Columbia, MO 65211 USA
[2] Univ Missouri, Res Cath Lab, Columbia, MO 65211 USA
[3] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65211 USA
[4] Univ Missouri, Dept Med Pharmacol & Physiol, Columbia, MO 65211 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 296卷 / 05期
关键词
smooth muscle; migration; adventitia; SMOOTH-MUSCLE-CELLS; RAT CAROTID ARTERIES; GENE-TRANSFER; GROWTH-FACTOR; MIGRATION; INJURY; PROLIFERATION; BROMODEOXYURIDINE; ATHEROSCLEROSIS; APOPTOSIS;
D O I
10.1152/ajpheart.00566.2008
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Fleenor BS, Bowles DK. Negligible contribution of coronary adventitial fibroblasts to neointimal formation following balloon angioplasty in swine. Am J Physiol Heart Circ Physiol 296: H1532-H1539, 2009. First published February 27, 2009; doi:10.1152/ajpheart.00566.2008.-Adventitial fibroblasts have previously been proposed to be a major constituent of the neointima following coronary balloon angioplasty. The present study utilized the bromodeoxyuridine (BrdU) pulse-chase technique to track adventitial fibroblast migration early after balloon injury in swine. BrdU (30 mg/kg), a marker of proliferating cells, was given intravenously 1 or 2 days after balloon angioplasty. For each time point, one animal was euthanized 24 h after injection to identify the location of the proliferating cells, while a second animal was euthanized 25 days after angioplasty to determine whether the proliferating cells migrated to form the neointima. Our results demonstrate that BrdU-positive cells were located primarily in the adventitia with all three time points 24 h after balloon angioplasty. Furthermore, when BrdU was injected on day 1 or 2 only 0.65 +/- 0.17% and 1.7 +/- 0.64%, respectively, of neointimal cells were BrdU positive on day 25. In conclusion, these results demonstrate a negligible contribution of coronary adventitial fibroblasts to neointima formation following coronary balloon angioplasty, supporting the concept that the neointima is primarily of smooth muscle cell origin.
引用
收藏
页码:H1532 / H1539
页数:8
相关论文
共 25 条
[1]
Smooth muscle cells in atherosclerosis originate from the local vessel wall and not circulating progenitor cells in ApoE knockout mice [J].
Bentzon, Jacob F. ;
Weile, Charlotte ;
Sondergaard, Claus S. ;
Hindkjaer, Johnny ;
Kassem, Moustapha ;
Falk, Erling .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (12) :2696-2702
[2]
Mechanisms of neointima formation and remodeling in the porcine coronary artery [J].
Christen, T ;
Verin, V ;
Bochaton-Piallat, ML ;
Popowski, Y ;
Ramaekers, F ;
Debruyne, P ;
Camenzind, E ;
van Eys, G ;
Gabbiani, G .
CIRCULATION, 2001, 103 (06) :882-888
[3]
SIGNIFICANCE OF QUIESCENT SMOOTH-MUSCLE MIGRATION IN THE INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
SCHWARTZ, SM .
CIRCULATION RESEARCH, 1985, 56 (01) :139-145
[4]
Adventitial cells do not contribute to neointimal mass after balloon angioplasty of the rat common carotid artery [J].
De Leon, H ;
Ollerenshaw, JD ;
Griendling, KK ;
Wilcox, JN .
CIRCULATION, 2001, 104 (14) :1591-1593
[5]
Smooth muscle-specific SM22 protein is expressed in the adventitial cells of balloon-injured rabbit carotid artery [J].
Faggin, E ;
Puato, M ;
Zardo, L ;
Franch, R ;
Millino, C ;
Sarinella, F ;
Pauletto, P ;
Sartore, S ;
Chiavegato, A .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (06) :1393-1404
[6]
PLATELET-DERIVED GROWTH-FACTOR PROMOTES SMOOTH-MUSCLE MIGRATION AND INTIMAL THICKENING IN A RAT MODEL OF BALLOON ANGIOPLASTY [J].
JAWIEN, A ;
BOWENPOPE, DF ;
LINDNER, V ;
SCHWARTZ, SM ;
CLOWES, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (02) :507-511
[7]
KRISS JP, 1962, CANCER RES, V22, P254
[8]
Direct in vivo evidence demonstrating neointimal migration of adventitial fibroblasts after balloon injury of rat carotid arteries [J].
Li, GH ;
Chen, SJ ;
Oparil, S ;
Chen, YF ;
Thompson, JA .
CIRCULATION, 2000, 101 (12) :1362-1365
[9]
Enhanced proliferation and migration and altered cytoskeletal proteins in early passage smooth muscle cells from young and old rat aortic explants [J].
Li, ZH ;
Cheng, HP ;
Lederer, WJ ;
Froehlich, J ;
Lakatta, EG .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1997, 64 (01) :1-11
[10]
Apoptosis and cell proliferation after porcine coronary angioplasty [J].
Malik, N ;
Francis, SE ;
Holt, CM ;
Gunn, J ;
Thomas, GL ;
Shepherd, L ;
Chamberlain, J ;
Newman, CMH ;
Cumberland, DC ;
Crossman, DC .
CIRCULATION, 1998, 98 (16) :1657-1665