Inflammation in atherosclerosis: pathophysiology and mechanisms

被引:53
作者
Ajoolabady, Amir [1 ]
Pratico, Domenico [2 ]
Lin, Ling [3 ,4 ]
Mantzoros, Christos S. [5 ]
Bahijri, Suhad [6 ]
Tuomilehto, Jaakko [6 ,7 ,8 ]
Ren, Jun [3 ,4 ]
机构
[1] Univ Alabama Birmingham, Dept Biomed Engn, Birmingham, AL 35294 USA
[2] Temple Univ, Alzheimers Ctr Temple, Lewis Katz Sch Med, Philadelphia, PA 19140 USA
[3] Fudan Univ, Shanghai Inst Cardiovasc Dis, Zhongshan Hosp, Dept Cardiol, Shanghai 200032, Peoples R China
[4] Natl Clin Res Ctr Intervent Med, Shanghai 200032, Peoples R China
[5] Harvard Univ, Harvard Med Sch, Boston, MA 02115 USA
[6] King Abdulaziz Univ, Diabet Res Grp, Jeddah, Saudi Arabia
[7] Univ Helsinki, Dept Publ Hlth, Helsinki, Finland
[8] Finnish Inst Hlth & Welf, Hlth Promot Unit, Helsinki, Finland
关键词
REVERSE CHOLESTEROL TRANSPORT; RESOLVING LIPID MEDIATORS; MACROPHAGE POLARIZATION; MYOCARDIAL-INFARCTION; VASCULAR ENDOTHELIUM; SCAVENGER RECEPTORS; NLRP3; INFLAMMASOME; PPAR-GAMMA; INHIBITION; LDL;
D O I
10.1038/s41419-024-07166-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Atherosclerosis imposes a heavy burden on cardiovascular health due to its indispensable role in the pathogenesis of cardiovascular disease (CVD) such as coronary artery disease and heart failure. Ample clinical and experimental evidence has corroborated the vital role of inflammation in the pathophysiology of atherosclerosis. Hence, the demand for preclinical research into atherosclerotic inflammation is on the horizon. Indeed, the acquisition of an in-depth knowledge of the molecular and cellular mechanisms of inflammation in atherosclerosis should allow us to identify novel therapeutic targets with translational merits. In this review, we aimed to critically discuss and speculate on the recently identified molecular and cellular mechanisms of inflammation in atherosclerosis. Moreover, we delineated various signaling cascades and proinflammatory responses in macrophages and other leukocytes that promote plaque inflammation and atherosclerosis. In the end, we highlighted potential therapeutic targets, the pros and cons of current interventions, as well as anti-inflammatory and atheroprotective mechanisms.
引用
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页数:16
相关论文
共 178 条
[51]   TRAIL promotes the polarization of human macrophages toward a proinflammatory M1 phenotype and is associated with increased survival in cancer patients with high tumor macrophage content [J].
Gunalp, Sinem ;
Helvaci, Derya Goksu ;
Oner, Aysenur ;
Bursali, Ahmet ;
Conforte, Alessandra ;
Guener, Hueseyin ;
Karakulah, Gokhan ;
Szegezdi, Eva ;
Sag, Duygu .
FRONTIERS IN IMMUNOLOGY, 2023, 14
[52]  
Guo FX, 2020, AM J CANCER RES, V10, P3285
[53]   CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis [J].
Guo, Liang ;
Akahori, Hirokuni ;
Harari, Emanuel ;
Smith, Samantha L. ;
Polavarapu, Rohini ;
Karmali, Vinit ;
Otsuka, Fumiyuki ;
Gannon, Rachel L. ;
Braumann, Ryan E. ;
Dickinson, Megan H. ;
Gupta, Anuj ;
Jenkins, Audrey L. ;
Lipinski, Michael J. ;
Kim, Johoon ;
Chhour, Peter ;
de Vries, Paul S. ;
Jinnouchi, Hiroyuki ;
Kutys, Robert ;
Mori, Hiroyoshi ;
Kutyna, Matthew D. ;
Torii, Sho ;
Sakamoto, Atsushi ;
Choi, Cheol Ung ;
Cheng, Qi ;
Grove, Megan L. ;
Sawan, Mariem A. ;
Zhang, Yin ;
Cao, Yihai ;
Kolodgie, Frank D. ;
Cormode, David P. ;
Arking, Dan E. ;
Boerwinkle, Eric ;
Morrison, Alanna C. ;
Erdmann, Jeanette ;
Sotoodehnia, Nona ;
Virmani, Renu ;
Finn, Aloke V. .
JOURNAL OF CLINICAL INVESTIGATION, 2018, 128 (03) :1106-1124
[54]   The Dendritic Cell Receptor DNGR-1 Promotes the Development of Atherosclerosis in Mice [J].
Haddad, Yacine ;
Lahoute, Charlotte ;
Clement, Marc ;
Laurans, Ludivine ;
Metghalchi, Sarvenaz ;
Zeboudj, Lynda ;
Giraud, Andreas ;
Loyer, Xavier ;
Vandestienne, Marie ;
Wain-Hobson, Julien ;
Esposito, Bruno ;
Potteaux, Stephane ;
Ait-Oufella, Hafid ;
Tedgui, Alain ;
Mallat, Ziad ;
Taleb, Soraya .
CIRCULATION RESEARCH, 2017, 121 (03) :234-+
[55]   Follicle-Stimulating Hormone Provokes Macrophages to Secrete IL-1b Contributing to Atherosclerosis Progression [J].
Han, Jing-li ;
Song, Yu-xuan ;
Yao, Wei-juan ;
Zhou, Jing ;
Du, Yiqing ;
Xu, Tao .
JOURNAL OF IMMUNOLOGY, 2023, 210 (01) :25-32
[56]   Atherosclerosis-prone hemodynamics differentially regulates endothelial and smooth muscle cell phenotypes and promotes pro-inflammatory priming [J].
Hastings, Nicole E. ;
Simmers, Michael B. ;
McDonald, Oliver G. ;
Wamhoff, Brian R. ;
Blackman, Brett R. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2007, 293 (06) :C1824-C1833
[57]   PPARgamma in Metabolism, Immunity, and Cancer: Unified and Diverse Mechanisms of Action [J].
Hernandez-Quiles, Miguel ;
Broekema, Marjoleine F. ;
Kalkhoven, Eric .
FRONTIERS IN ENDOCRINOLOGY, 2021, 12
[58]   Coronary Atherosclerosis Is Associated With Macrophage Polarization in Epicardial Adipose Tissue [J].
Hirata, Yoichiro ;
Tabata, Minoru ;
Kurobe, Hirotsugu ;
Motoki, Tatsuo ;
Akaike, Masashi ;
Nishio, Chika ;
Higashida, Mayuko ;
Mikasa, Hiroaki ;
Nakaya, Yutaka ;
Takanashi, Shuichiro ;
Igarashi, Takashi ;
Kitagawa, Tetsuya ;
Sata, Masataka .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2011, 58 (03) :248-255
[59]   Atherosclerotic intracranial arterial stenosis: risk factors, diagnosis, and treatment [J].
Holmstedt, Christine A. ;
Turan, Tanya N. ;
Chimowitz, Marc I. .
LANCET NEUROLOGY, 2013, 12 (11) :1106-1114
[60]   Thrombosis and atherosclerosis [J].
Holvoet, P ;
Collen, D .
CURRENT OPINION IN LIPIDOLOGY, 1997, 8 (05) :320-328