Macrophage Phenotype and Function in Different Stages of Atherosclerosis

被引:968
作者
Tabas, Ira [1 ,2 ,3 ]
Bornfeldt, Karin E. [4 ,5 ]
机构
[1] Columbia Univ, Dept Med, New York, NY USA
[2] Columbia Univ, Dept Anat & Cell Biol, New York, NY USA
[3] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY USA
[4] Univ Washington, UW Diabet Inst, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA 98109 USA
[5] Univ Washington, UW Diabet Inst, Dept Pathol, Seattle, WA 98109 USA
基金
美国国家卫生研究院;
关键词
macrophage; phenotype; atherosclerosis; foam cells; cholesterol; LOW-DENSITY-LIPOPROTEIN; FOAM CELL-FORMATION; SMOOTH-MUSCLE-CELLS; BINDING CASSETTE TRANSPORTERS; ENDOPLASMIC-RETICULUM STRESS; ACTIVATED RECEPTOR-GAMMA; TOLL-LIKE RECEPTORS; PROMOTES ATHEROSCLEROSIS; CHOLESTEROL ACCUMULATION; ACCELERATES ATHEROSCLEROSIS;
D O I
10.1161/CIRCRESAHA.115.306256
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The remarkable plasticity and plethora of biological functions performed by macrophages have enticed scientists to study these cells in relation to atherosclerosis for > 50 years, and major discoveries continue to be made today. It is now understood that macrophages play important roles in all stages of atherosclerosis, from initiation of lesions and lesion expansion, to necrosis leading to rupture and the clinical manifestations of atherosclerosis, to resolution and regression of atherosclerotic lesions. Lesional macrophages are derived primarily from blood monocytes, although recent research has shown that lesional macrophage-like cells can also be derived from smooth muscle cells. Lesional macrophages take on different phenotypes depending on their environment and which intracellular signaling pathways are activated. Rather than a few distinct populations of macrophages, the phenotype of the lesional macrophage is more complex and likely changes during the different phases of atherosclerosis and with the extent of lipid and cholesterol loading, activation by a plethora of receptors, and metabolic state of the cells. These different phenotypes allow the macrophage to engulf lipids, dead cells, and other substances perceived as danger signals; efflux cholesterol to high-density lipoprotein; proliferate and migrate; undergo apoptosis and death; and secrete a large number of inflammatory and proresolving molecules. This review article, part of the Compendium on Atherosclerosis, discusses recent advances in our understanding of lesional macrophage phenotype and function in different stages of atherosclerosis. With the increasing understanding of the roles of lesional macrophages, new research areas and treatment strategies are beginning to emerge.
引用
收藏
页码:653 / 667
页数:15
相关论文
共 141 条
[1]   Massive xanthomatosis and altered composition of atherosclerotic lesions in hyperlipidemic mice lacking acyl CoA:cholesterol acyltransferase 1 [J].
Accad, M ;
Smith, SJ ;
Newland, DL ;
Sanan, DA ;
King, LE ;
Linton, MF ;
Fazio, S ;
Farese, RV .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (06) :711-719
[2]   Signal transducer and activator of transcription 1 is required for optimal foam cell formation and atherosclerotic lesion development [J].
Agrawal, Sudesh ;
Febbraio, Maria ;
Podrez, Eugene ;
Cathcart, Martha K. ;
Stark, George R. ;
Chisolm, Guy M. .
CIRCULATION, 2007, 115 (23) :2939-2947
[3]   Contribution of Intimal Smooth Muscle Cells to Cholesterol Accumulation and Macrophage-Like Cells in Human Atherosclerosis [J].
Allahverdian, Sima ;
Chehroudi, Ali Cyrus ;
McManus, Bruce M. ;
Abraham, Thomas ;
Francis, Gordon A. .
CIRCULATION, 2014, 129 (15) :1551-1559
[4]   Macrophage expression of peroxisome proliferator-activated receptor-α reduces atherosclerosis in low-density lipoprotein receptor-deficient mice [J].
Babaev, Vladimir R. ;
Ishiguro, Hiroyuki ;
Ding, Lei ;
Yancey, Patricia G. ;
Dove, Dwayne E. ;
Kovacs, William J. ;
Semenkovich, Clay F. ;
Fazio, Sergio ;
Linton, MacRae F. .
CIRCULATION, 2007, 116 (12) :1404-1412
[5]   Macrophage Mal1 Deficiency Suppresses Atherosclerosis in Low-Density Lipoprotein Receptor-Null Mice by Activating Peroxisome Proliferator-Activated Receptor-γ-Regulated Genes [J].
Babaev, Vladimir R. ;
Runner, Robert P. ;
Fan, Daping ;
Ding, Lei ;
Zhang, Youmin ;
Tao, Huan ;
Erbay, Ebru ;
Goerguen, Cem Z. ;
Fazio, Sergio ;
Hotamisligil, Goekhan S. ;
Linton, MacRae F. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2011, 31 (06) :1283-U83
[6]   PPARδ regulates multiple proinflammatory pathways to suppress atherosclerosis [J].
Barish, Grant D. ;
Atkins, Annette R. ;
Downes, Michael ;
Olson, Peter ;
Chong, Ling-Wa ;
Nelson, Mike ;
Zou, Yuhua ;
Hwang, Hoosang ;
Kang, Heonjoong ;
Curtiss, Linda ;
Evans, Ronald M. ;
Lee, Chih-Hao .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (11) :4271-4276
[7]   Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2010, 11 (10) :889-896
[8]   A leukocyte homologue of the IL-8 receptor CXCR-2 mediates the accumulation of macrophages in atherosclerotic lesions of LDL receptor-deficient mice [J].
Boisvert, WA ;
Santiago, R ;
Curtiss, LK ;
Terkeltaub, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :353-363
[9]   Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis [J].
Boring, L ;
Gosling, J ;
Cleary, M ;
Charo, IF .
NATURE, 1998, 394 (6696) :894-897
[10]   Coronary Intraplaque Hemorrhage Evokes a Novel Atheroprotective Macrophage Phenotype [J].
Boyle, Joseph J. ;
Harrington, Heather A. ;
Piper, Emma ;
Elderfield, Kay ;
Stark, Jaroslav ;
Landis, Robert C. ;
Haskard, Dorian O. .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (03) :1097-1108