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Platelet-Derived MRP-14 Induces Monocyte Activation in Patients With Symptomatic Peripheral Artery Disease
Authors:Rebecca Dann  Tarik Hadi  Emilie Montenont  Ludovic Boytard  Dornaszadat Alebrahim  Jordyn Feinstein  Nicole Allen  Russell Simon  Krista Barone  Kunihiro Uryu  Yu Guo  Caron Rockman  Bhama Ramkhelawon  Jeffrey S. Berger
Affiliation:1. Divisions of Cardiology and Hematology, Department Medicine, New York University School of Medicine, New York, New York;2. Division of Vascular Surgery, Department of Surgery, New York University School of Medicine, New York, New York;3. Electron Microscopy Resource Center, The Rockefeller University, New York, New York;4. Department of Cell Biology, New York University School of Medicine, New York, New York
Abstract:

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)
Keywords:macrophages  monocytes  peripheral artery disease  platelet–monocyte aggregates  platelets  CAS  carotid artery stenosis  CLI  critical limb ischemia  LPA  leukocyte–platelet aggregate(s)  MACLE  major adverse cardiovascular and limb events  MPA  monocyte–platelet aggregate(s)  MRP  myeloid-related protein  PAD  peripheral artery disease  PR  platelet releasate
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