Macrophage Apoptosis Exerts Divergent Effects on Atherogenesis as a Function of Lesion Stage

被引:209
作者
Gautier, Emmanuel L. [2 ]
Huby, Thierry [2 ,3 ]
Witztum, Joseph L. [5 ]
Ouzilleau, Betty [2 ]
Miller, Elizabeth R. [5 ]
Saint-Charles, Flora [2 ]
Aucouturier, Pierre [2 ,4 ]
Chapman, M. John [2 ,3 ]
Lesnik, Philippe [1 ,2 ,3 ]
机构
[1] Hop Pitie, INSERM, U939, UMR S939, F-75651 Paris 13, France
[2] UPMC Univ Paris, Paris, France
[3] Grp Hosp Pitie Salpetriere, AP HP, Serv Endocrinol Metab, F-75634 Paris, France
[4] Hop St Antoine, INSERM, UMR S 938, F-75571 Paris, France
[5] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
关键词
atherosclerosis; cholesterol; inflammation; leukocytes; macrophages; pathology; survival; E-DEFICIENT MICE; ACCELERATED ATHEROSCLEROSIS; OXIDIZED LDL; T-CELLS; INFLAMMATION; EXPRESSION; PLAQUE; PHAGOCYTOSIS; PROGRESSION; ACTIVATION;
D O I
10.1161/CIRCULATIONAHA.108.806158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Because apoptotic cell clearance appears to be defective in advanced compared with early atherosclerotic plaques, macrophage apoptosis may differentially affect plaque progression as a function of lesion stage. Methods and Results-We first evaluated the impact of targeted protection of macrophages against apoptosis at both early and advanced stages of atherosclerosis. Increased resistance of macrophages to apoptosis in early atherosclerotic lesions was associated with increased plaque burden; in contrast, it afforded protection against progression to advanced lesions. Conversely, sustained induction of apoptosis in lesional macrophages of advanced lesions resulted in a significant increase in lesion size. Such enhanced lesion size occurred as a result not only of apoptotic cell accumulation but also of elevated chemokine expression and subsequent intimal recruitment of circulating monocytes. Conclusions-Considered together, our data suggest that macrophage apoptosis is atheroprotective in fatty streak lesions, but in contrast, defective clearance of apoptotic debris in advanced lesions favors arterial wall inflammation and enhanced recruitment of monocytes, leading to enhanced atherogenesis. (Circulation. 2009; 119: 1795-1804.)
引用
收藏
页码:1795 / U186
页数:23
相关论文
共 30 条
[1]   Lactadherin deficiency leads to apoptotic cell accumulation and accelerated atherosclerosis in mice [J].
Ait-Oufella, Hafid ;
Kinugawa, Kiyoka ;
Zoll, Joffrey ;
Simon, Tabassome ;
Boddaert, Jacques ;
Heeneman, Silvia ;
Blanc-Brude, Olivier ;
Barateau, Veronique ;
Potteaux, Stephane ;
Merval, Regine ;
Esposito, Bruno ;
Teissier, Elisabeth ;
Daemen, Mat J. ;
Leseche, Guy ;
Boulanger, Chantal ;
Tedgui, Alain ;
Mallat, Ziad .
CIRCULATION, 2007, 115 (16) :2168-2177
[2]   A role for the apoptosis inhibitory factor AIM/Spα/Api6 in atherosclerosis development [J].
Arai, S ;
Shelton, JM ;
Chen, MY ;
Bradley, MN ;
Castrillo, A ;
Bookout, AL ;
Mak, PA ;
Edwards, PA ;
Mangelsdorf, DJ ;
Tontonoz, P ;
Miyazaki, T .
CELL METABOLISM, 2005, 1 (03) :201-213
[3]   Endothelial cell regulation by phospholipid oxidation products [J].
Berliner, Judith A. ;
Gharavi, Nima M. .
FREE RADICAL BIOLOGY AND MEDICINE, 2008, 45 (02) :119-123
[4]   IL-5 links adaptive and natural immunity specific for epitopes of oxidized LDL and protects from atherosclerosis [J].
Binder, CJ ;
Hartvigsen, K ;
Chang, MK ;
Miller, M ;
Broide, D ;
Palinski, W ;
Curtiss, LK ;
Corr, M ;
Witztum, JL .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (03) :427-437
[5]   Pneumococcal vaccination decreases atherosclerotic lesion formation:: molecular mimicry between Streptococcus pneumoniae and oxidized LDL [J].
Binder, CJ ;
Hörkkö, S ;
Dewan, A ;
Chang, MK ;
Kieu, EP ;
Goodyear, CS ;
Shaw, PX ;
Palinski, W ;
Witztum, JL ;
Silverman, GJ .
NATURE MEDICINE, 2003, 9 (06) :736-743
[6]   Apoptotic cells with oxidation-specific epitopes are immunogenic and proinflammatory [J].
Chang, MK ;
Binder, CJ ;
Miller, YI ;
Subbanagounder, G ;
Silverman, GJ ;
Berliner, JA ;
Witztum, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (11) :1359-1370
[7]  
Farhadi HF, 2003, J NEUROSCI, V23, P10214
[8]   The endoplasmic reticulum is the site of cholesterol-induced cytotoxicity in macrophages [J].
Feng, B ;
Yao, PM ;
Li, YK ;
Devlin, CM ;
Zhang, DJ ;
Harding, HP ;
Sweeney, M ;
Rong, JX ;
Kuriakose, G ;
Fisher, EA ;
Marks, AR ;
Ron, D ;
Tabas, I .
NATURE CELL BIOLOGY, 2003, 5 (09) :781-792
[9]   Oxidized phospholipids trigger atherogenic inflammation in murine arteries [J].
Furnkranz, A ;
Schober, A ;
Bochkov, VN ;
Bashtrykov, P ;
Kronke, G ;
Kadl, A ;
Binder, BR ;
Weber, C ;
Leitinger, N .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (03) :633-638
[10]   Enhanced dendritic cell survival attenuates lipopolysaccharide-induced immunosuppression and increases resistance to lethal endotoxic shock [J].
Gautier, Emmanuel L. ;
Huby, Thierry ;
Saint-Charles, Flora ;
Ouzilleau, Betty ;
Chapman, M. John ;
Lesnik, Philippe .
JOURNAL OF IMMUNOLOGY, 2008, 180 (10) :6941-6946