Delineation of the evolution of compositional changes in atheroma

被引:16
作者
Wadsworth, MP
Sobel, BE
Schneider, DJ
Taatjes, DJ
机构
[1] Univ Vermont, Coll Med, Dept Pathol, Burlington, VT 05405 USA
[2] Univ Vermont, Coll Med, Dept Med, Burlington, VT 05405 USA
[3] Univ Vermont, Coll Med, Microscopy Imaging Ctr, Burlington, VT 05405 USA
关键词
atherosclerosis; plaque composition; quantitation; computer-assisted microscopy;
D O I
10.1007/s00418-002-0419-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In a previous manuscript, we described a method combining immunohistochemistry, confocal scanning laser microscopy, and computer-assisted image analysis for the determination of the composition of atherosclerotic plaques [Taatjes et al. (2000) Histochemistry and Cell Biology 113:161-173). We now present an enhanced technique, and its use for age- and gender-related comparative analysis of lesion composition in ApoE knockout mice. Cryosections from aorta were stained with oil red 0 to detect lipid, SYTOX Green to detect cellularity, and Picrosirius red to delineate collagen fibers. The stained sections were imaged by brightfield light microscopy, epifluorescence microscopy, and polarized light microscopy. Digital images were collected, processed to isolate the lesions, and subjected to computer-assisted image analysis. The average percentage of the vessel wall occupied by lesion increased 1.5-fold in animals from 10 to 20 weeks. Although the amount of lipid in the lesions increased in animals from 10 to 20 weeks, the percentage composition in the lesion remained constant because of the increase in lesion size. Average cellularity showed a modest decrease over the same interval. However, the percentage composition of plaque attributable to collagen increased 2.5-fold in 20-week-old female animals compared with that in males or females of 10 weeks of age and males of 20 weeks of a, e.
引用
收藏
页码:59 / 68
页数:10
相关论文
共 17 条
[1]  
DAVIES MJ, 1988, BRIT HEART J, V60, P459
[2]   CONVENTIONAL AND CONFOCAL FLUORESCENCE MICROSCOPY OF COLLAGEN-FIBERS IN THE HEART [J].
DOLBER, PC ;
SPACH, MS .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (03) :465-469
[3]   MORPHOLOGIC FEATURES OF UNSTABLE ATHEROTHROMBOTIC PLAQUES UNDERLYING ACUTE CORONARY SYNDROMES [J].
FALK, E .
AMERICAN JOURNAL OF CARDIOLOGY, 1989, 63 (10) :E114-E120
[4]   UNSTABLE ANGINA WITH FATAL OUTCOME - DYNAMIC CORONARY THROMBOSIS LEADING TO INFARCTION AND OR SUDDEN-DEATH - AUTOPSY EVIDENCE OF RECURRENT MURAL THROMBOSIS WITH PERIPHERAL EMBOLIZATION CULMINATING IN TOTAL VASCULAR OCCLUSION [J].
FALK, E .
CIRCULATION, 1985, 71 (04) :699-708
[5]   PICROSIRIUS STAINING PLUS POLARIZATION MICROSCOPY, A SPECIFIC METHOD FOR COLLAGEN DETECTION IN TISSUE-SECTIONS [J].
JUNQUEIRA, LCU ;
BIGNOLAS, G ;
BRENTANI, RR .
HISTOCHEMICAL JOURNAL, 1979, 11 (04) :447-455
[6]   Effects of troglitazone on blood concentrations of plasminogen activator inhibitor 1 in patients with type 2 diabetes and in lean and obese normal subjects [J].
Kruszynska, YT ;
Yu, JG ;
Olefsky, JM ;
Sobel, BE .
DIABETES, 2000, 49 (04) :633-639
[7]   FACTORS RESPONSIBLE FOR IMPAIRED FIBRINOLYSIS IN OBESE SUBJECTS AND NIDDM PATIENTS [J].
MCGILL, JB ;
SCHNEIDER, DJ ;
ARFKEN, CL ;
LUCORE, CL ;
SOBEL, BE .
DIABETES, 1994, 43 (01) :104-109
[8]   Sirius red and acid fuchsin staining mechanisms [J].
Nielsen, LF ;
Moe, D ;
Kirkeby, S ;
Garbarsch, C .
BIOTECHNIC & HISTOCHEMISTRY, 1998, 73 (02) :71-77
[9]   INDUCTION OF PLASMINOGEN-ACTIVATOR INHIBITOR TYPE-1 (PAI-1) BY PROINSULIN AND INSULIN IN-VIVO [J].
NORDT, TK ;
SAWA, H ;
FUJII, S ;
SOBEL, BE .
CIRCULATION, 1995, 91 (03) :764-770
[10]   QUANTITATIVE ASSESSMENT OF ATHEROSCLEROTIC LESIONS IN MICE [J].
PAIGEN, B ;
MORROW, A ;
HOLMES, PA ;
MITCHELL, D ;
WILLIAMS, RA .
ATHEROSCLEROSIS, 1987, 68 (03) :231-240