Changes in the pattern of plasma extracellular vesicles after severe trauma

被引:37
作者
Kuravi, Sahithi J. [1 ,2 ]
Yates, Clara M. [1 ,2 ]
Foster, Mark [2 ]
Harrison, Paul [3 ]
Hazeldine, Jon [2 ,3 ]
Hampson, Peter [3 ]
Watson, Chris [4 ]
Belli, Antonio [2 ,3 ]
Midwinter, Mark [2 ,5 ]
Nash, Gerard B. [1 ,2 ]
机构
[1] Univ Birmingham, Inst Cardiovasc Sci, Coll Med & Dent Sci, Birmingham, W Midlands, England
[2] Univ Hosp Birmingham NHS Fdn Trust, NIHR Surg Reconstruct & Microbiol Res Ctr, Birmingham, W Midlands, England
[3] Univ Birmingham, Coll Med & Dent Sci, Inst Inflammat & Ageing, Birmingham, W Midlands, England
[4] Queen Elizabeth Hosp, Dept Haematol, Birmingham, W Midlands, England
[5] Univ Queensland, Fac Med, Rural Clin Sch Bundaberg, Bundaberg, Qld, Australia
关键词
CELL-DERIVED MICROPARTICLES; PROCOAGULANT MICROPARTICLES; CIRCULATING MICROPARTICLES; PLATELET MICROPARTICLES; ORGAN DYSFUNCTION; GLYCOPROTEIN IB; FLOW-CYTOMETRY; MICROVESICLES; BLOOD; STANDARDIZATION;
D O I
10.1371/journal.pone.0183640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Extracellular vesicles (EV) released into the circulation after traumatic injury may influence complications. We thus evaluated the numbers of EV in plasma over 28 days after trauma and evaluated their pro-coagulant and inflammatory effects. Methods and findings 37 patients suffering trauma with an injury severity score > 15 were studied along with 24 healthy controls. Plasma samples were isolated by double centrifugation (2000g 20min; 13000g 2min) from blood collected from within an hour up to 28 days after injury. Plasma EV were counted and sized using nanoparticle tracking analysis (NTA); counts and cellular origins were also determined by flow cytometry (FC) using cell-specific markers. Functional effects were tested in a procoagulant phospholipid assay and in flow-based, leukocyte adhesion assay after endothelial cells (EC) were treated with EV. We found that EV concentrations measured by NTA were significantly increased in trauma patients compared to healthy controls, and remained elevated over days. In addition, or FC showed that patients with trauma had higher numbers of EV derived from platelets (CD41+), leukocytes (CD45+) and endothelial EC (CD144+). The increases were evident throughout the 28-day follow-up. However, the FC count represented <1% of the count detected by NTA, and only 1-2% of EV identified using NTA had a diameter > 400nm. The procoagulant phospholipid activity assay showed that patient plasma accelerated coagulation on day 1 and day 3 after trauma, with coagulation times correlated with EV counts. Furthermore, treatment of EC for 24 hours with plasma containing EV tended to increase the recruitment of peripheral flowing blood mononuclear cells. Conclusions EV counted by FC represent a small sub-population of the total load detected by NTA. Both methods however indicate a significant increase in plasma EV after severe traumatic injury that have pro-coagulant and pro-inflammatory effects that may influence outcomes.
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页数:17
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