Role of LOX-1 (Lectin-Like Oxidized Low-Density Lipoprotein Receptor 1) as a Cardiovascular Risk Predictor: Mechanistic Insight and Potential Clinical Use

被引:115
作者
Barreto, Joaquim [1 ]
Karathanasis, Sotirios K. [2 ,3 ]
Remaley, Alan [2 ]
Sposito, Andrei C. [1 ]
机构
[1] State Univ Campinas UNICAMP, Fac Med Sci, Clin Res Ctr, Atherosclerosis & Vasc Biol Lab Atherolab, Campinas, Brazil
[2] NHLBI, NIH, Bldg 10, Bethesda, MD 20892 USA
[3] NeoProgen, Baltimore, MD USA
关键词
acute coronary syndrome; atherosclerosis; cardiovascular disease; myocardial infarction; platelet activation; ARTERY ENDOTHELIAL-CELLS; LDL RECEPTOR-1; OX-LDL; UP-REGULATION; MYOCARDIAL-INFARCTION; ISCHEMIA-REPERFUSION; CRYSTAL-STRUCTURE; LIGAND-BINDING; OLR1; GENE; ATHEROSCLEROSIS;
D O I
10.1161/ATVBAHA.120.315421
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis, the underlying cause of cardiovascular disease (CVD), is a worldwide cause of morbidity and mortality. Reducing ApoB-containing lipoproteins-chiefly, LDL (low-density lipoprotein)-has been the main strategy for reducing CVD risk. Although supported by large randomized clinical trials, the persistence of residual cardiovascular risk after effective LDL reduction has sparked an intense search for other novel CVD biomarkers and therapeutic targets. Recently, Lox-1 (lectin-type oxidized LDL receptor 1), an innate immune scavenger receptor, has emerged as a promising target for early diagnosis and cardiovascular risk prediction and is also being considered as a treatment target. Lox-1 was first described as a 50 kDa transmembrane protein in endothelial cells responsible for oxLDL (oxidized LDL) recognition, triggering downstream pathways that intensify atherosclerosis via endothelial dysfunction, oxLDL uptake, and apoptosis. Lox-1 is also expressed in platelets, where it enhances platelet activation, adhesion to endothelial cells, and ADP-mediated aggregation, thereby favoring thrombus formation. Lox-1 was also identified in cardiomyocytes, where it was implicated in the development of cardiac fibrosis and myocyte apoptosis, the main determinants of cardiac recovery following an ischemic insult. Together, these findings have revealed that Lox-1 is implicated in all the main steps of atherosclerosis and has encouraged the development of immunoassays for measurement of sLox-1 (serum levels of soluble Lox-1) to be used as a potential CVD biomarker. Finally, the recent development of synthetic Lox-1 inhibitors and neutralizing antibodies with promising results in animal models has made Lox-1 a target for drug development. In this review, we discuss the main findings regarding the role of Lox-1 in the development, diagnosis, and therapeutic strategies for CVD prevention and treatment.
引用
收藏
页码:153 / 166
页数:14
相关论文
共 115 条
[91]   Ox-LDL-induced LOX-1 expression in vascular smooth muscle cells: role of reactive oxygen species [J].
Sun, Yiyi ;
Chen, Xiuping .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2011, 25 (05) :572-579
[92]   Subendothelial lipoprotein retention as the initiating process in atherosclerosis -: Update and therapeutic implications [J].
Tabas, Ira ;
Williams, Kevin Jon ;
Boren, Jan .
CIRCULATION, 2007, 116 (16) :1832-1844
[93]   Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction [J].
Tatsuguchi, M ;
Furutani, M ;
Hinagata, J ;
Tanaka, T ;
Furutani, Y ;
Imamura, S ;
Kawana, M ;
Masaki, T ;
Kasanuki, H ;
Sawamura, T ;
Matsuoka, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (01) :247-250
[94]  
Thygesen K, 2012, CIRCULATION, V126, P2020, DOI [10.1093/eurheartj/ehs184, 10.1161/CIR.0b013e31826e1058, 10.1016/j.jacc.2012.08.001, 10.1016/j.gheart.2018.08.004, 10.1016/j.clinbiochem.2012.10.036, 10.1016/j.gheart.2012.08.001, 10.5603/KP.2018.0203]
[95]   Targeting LOX-1 in atherosclerosis and vasculopathy: current knowledge and future perspectives [J].
Tian, Kunming ;
Ogura, Sayoko ;
Little, Peter J. ;
Xu, Suo-wen ;
Sawamura, Tatsuya .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 2019, 1443 (01) :34-53
[96]   On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease [J].
Trabetti, E ;
Biscuola, M ;
Cavallari, U ;
Malerba, G ;
Girelli, D ;
Olivieri, O ;
Martinelli, N ;
Corrocher, R ;
Pignatti, PF .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (01) :127-130
[97]   Transcytosis: Crossing cellular barriers [J].
Tuma, PL ;
Hubbard, AL .
PHYSIOLOGICAL REVIEWS, 2003, 83 (03) :871-932
[98]   Overexpression of LOXIN Protects Endothelial Progenitor Cells From Apoptosis Induced by Oxidized Low Density Lipoprotein [J].
Veas, Carlos ;
Jara, Casandra ;
Willis, Naomi D. ;
Perez-Contreras, Karen ;
Gutierrez, Nicolas ;
Toledo, Jorge ;
Fernandez, Paulina ;
Radojkovic, Claudia ;
Zuniga, Felipe A. ;
Escudero, Carlos ;
Aguayo, Claudio .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2016, 67 (04) :326-335
[99]  
Vecchione Lucia, 2007, Recent Pat Cardiovasc Drug Discov, V2, P147
[100]   Pro-fibrotic effect of oxidized LDL in cardiac myofibroblasts [J].
Villa, Monica ;
Cerda-Opazo, Paulina ;
Jimenez-Gallegos, Danica ;
Garrido-Moreno, Valeria ;
Chiong, Mario ;
Quest, Andrew Fg ;
Toledo, Jorge ;
Garcia, Lorena .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2020, 524 (03) :696-701