Platelet-Derived MRP-14 Induces Monocyte Activation in Patients With Symptomatic Peripheral Artery Disease

被引:58
作者
Dann, Rebecca [1 ,2 ]
Hadi, Tarik [3 ]
Montenont, Emilie [1 ,2 ]
Boytard, Ludovic [3 ]
Alebrahim, Dornaszadat [3 ]
Feinstein, Jordyn [3 ]
Allen, Nicole [1 ,2 ]
Simon, Russell [3 ]
Barone, Krista [3 ]
Uryu, Kunihiro [4 ]
Guo, Yu [1 ,2 ]
Rockman, Caron [3 ]
Ramkhelawon, Bhama [3 ,5 ]
Berger, Jeffrey S. [1 ,2 ,3 ]
机构
[1] NYU, Sch Med, Dept Med, Div Cardiol, 530 First Ave, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Med, Div Hematol, 530 First Ave, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Surg, Div Vasc Surg, 530 First Ave, New York, NY 10016 USA
[4] Rockefeller Univ, Electron Microscopy Resource Ctr, 1230 York Ave, New York, NY 10021 USA
[5] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
关键词
macrophages; monocytes; peripheral artery disease; platelet-monocyte aggregates; platelets; ATHEROTHROMBOSIS; INFLAMMATION; ATHEROSCLEROSIS; EXPRESSION; ATHEROGENESIS; COAGULATION; PROTEIN-14; THROMBOSIS; EVENTS; MICE;
D O I
10.1016/j.jacc.2017.10.072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Peripheral artery disease (PAD), a diffuse manifestation of atherothrombosis, is a major cardiovascular threat. Although platelets are primary mediators of atherothrombosis, their role in the pathogenesis of PAD remains unclear. OBJECTIVES The authors sought to investigate the role of platelets in a cohort of symptomatic PAD. METHODS The authors profiled platelet activity, mRNA, and effector roles in patients with symptomatic PAD and in healthy controls. Patients with PAD and carotid artery stenosis were recruited into ongoing studies (NCT02106429 and NCT01897103) investigating platelet activity, platelet RNA, and cardiovascular disease. RESULTS Platelet RNA sequence profiling mapped a robust up-regulation of myeloid-related protein (MRP)-14 mRNA, a potent calcium binding protein heterodimer, in PAD. Circulating activated platelets were enriched with MRP-14 protein, which augmented the expression of the adhesion mediator, P-selectin, thereby promoting monocyte-platelet aggregates. Electron microscopy confirmed the firm interaction of platelets with monocytes in vitro and colocalization of macrophages with MRP-14 confirmed their cross talk in atherosclerotic manifestations of PAD in vivo. Platelet-derived MRP-14 was channeled to monocytes, thereby fueling their expression of key PAD lesional hallmarks and increasing their directed locomotion, which were both suppressed in the presence of antibody-mediated blockade. Circulating MRP-14 was heightened in the setting of PAD, significantly correlated with PAD severity, and was associated with incident limb events. CONCLUSIONS The authors identified a heightened platelet activity profile and unraveled a novel immunomodulatory effector role of platelet-derived MRP-14 in reprograming monocyte activation in symptomatic PAD. (Platelet Activity in Vascular Surgery and Cardiovascular Events [PACE]; NCT02106429; and Platelet Activity in Vascular Surgery for Thrombosis and Bleeding [PIVOTAL]; NCT01897103) (c) 2018 by the American College of Cardiology Foundation.
引用
收藏
页码:53 / 65
页数:13
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