Macrophage foam cells and atherosclerosis

被引:81
作者
Kruth, HS [1 ]
机构
[1] NHLBI, Sect Expt Atherosclerosis, NIH, Bethesda, MD 20892 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2001年 / 6卷
关键词
atherosclerosis; cholesterol; lipoproteins; macrophage; vessels; lipids; metabolism; review;
D O I
10.2741/Kruth
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Focal buildup of cholesterol in arteries is the process that produces atherosclerotic plaques, the cause of most coronary artery disease and strokes. Monocyte-derived macrophages are central cells that accumulate this cholesterol in atherosclerotic lesions, a manifestation of the scavenging function of the macrophage. Different types of cholesterol-containing lipid particles found in atherosclerotic lesions may enter macrophages by a variety of endocytic pathways. The fate of cholesterol that enters macrophages determines whether macrophages help or hinder cholesterol removal from the vessel wall. Macrophages may function to carry cholesterol out of lesions, or to process the cholesterol for excretion in association with small protein-phospholipid complexes. Alternatively, macrophages that do not efficiently function to remove cholesterol from lesions may ultimately undergo cell death. Some cytokines, hormones, and pharmacologic agents show potential to modulate these processes and may be useful in directing macrophage function in atherosclerotic lesions towards beneficial rather than harmful effects.
引用
收藏
页码:D429 / D455
页数:27
相关论文
共 339 条
[1]  
ACTON SL, 1994, J BIOL CHEM, V269, P21003
[2]  
AIKAWA K, 1994, BBA-LIPID LIPID MET, V1213, P127
[3]   Inhibition of cholesteryl ester formation in macrophages by azole antimycotics [J].
Aikawa, K ;
Sato, Y ;
Furuchi, T ;
Ikemoto, M ;
Fujimoto, Y ;
Arai, H ;
Inoue, K .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (03) :447-453
[4]   CHOLESTEROL AND MORTALITY - 30 YEARS OF FOLLOW-UP FROM THE FRAMINGHAM-STUDY [J].
ANDERSON, KM ;
CASTELLI, WP ;
LEVY, D .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1987, 257 (16) :2176-2180
[5]  
ANGELIN B, 1987, ACTA MED SCAND, P45
[6]  
Anitschkow N, 1913, ZENTRALBL ALLG PATHO, V24, P1
[7]   IDENTIFICATION OF MACROPHAGES AND SMOOTH-MUSCLE CELLS IN HUMAN ATHEROSCLEROSIS USING MONOCLONAL-ANTIBODIES [J].
AQEL, NM ;
BALL, RY ;
WALDMANN, H ;
MITCHINSON, MJ .
JOURNAL OF PATHOLOGY, 1985, 146 (03) :197-204
[8]   AGE-RELATED-CHANGES IN THE METABOLISM OF ACETYLATED LOW-DENSITY LIPOPROTEINS BY PERITONEAL-MACROPHAGES FROM C57BL/6CRSCL MICE [J].
ARAKI, A ;
ITO, H ;
URANO, S ;
IIYAMA, M ;
SHIMADA, Y .
JOURNALS OF GERONTOLOGY, 1994, 49 (03) :B104-B109
[9]   Large variations in human foam cell formation in individuals: a fully autologous in vitro assay based on the quantitative analysis of cellular neutral lipids [J].
Asmis, R ;
Jelk, J .
ATHEROSCLEROSIS, 2000, 148 (02) :243-253
[10]   PHOSPHOLIPASE A2-MODIFIED LDL IS TAKEN UP AT ENHANCED RATE BY MACROPHAGES [J].
AVIRAM, M ;
MAOR, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 185 (01) :465-472