4.6 Article

The Platelet Lipidome Is Altered in Patients with COVID-19 and Correlates with Platelet Reactivity

期刊

THROMBOSIS AND HAEMOSTASIS
卷 122, 期 10, 页码 1683-1692

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0042-1749438

关键词

platelets; platelet activation; lipidomics; COVID-19; plasmalogens

资金

  1. Netherlands Organization for Health Research and Development (ZonMW) [50-53000-98-139]
  2. Assistance Publique des Hopitaux de Paris
  3. Fondation Bettencourt-Schueller
  4. JPI-AMR/ZonMW [547001008]
  5. Landsteiner Foundation (LSBR) [1901]
  6. NACTAR - Dutch Research Council (NWO) [16447]

向作者/读者索取更多资源

This study reveals the profound impact of COVID-19 infection on the lipid composition of human platelets, and identifies associations between platelet lipid composition and reactivity.
Background Activated platelets have been implicated in the proinflammatory and prothrombotic phenotype of coronavirus disease 2019 (COVID-19). While it is increasingly recognized that lipids have important structural and signaling roles in platelets, the lipidomic landscape of platelets during infection has remained unexplored. Objective To investigate the platelet lipidome of patients hospitalized for COVID-19. Methods We performed untargeted lipidomics in platelets of 25 patients hospitalized for COVID-19 and 23 noninfectious controls with similar age and sex characteristics, and with comparable comorbidities. Results Twenty-five percent of the 1,650 annotated lipids were significantly different between the groups. The significantly altered part of the platelet lipidome mostly comprised lipids that were less abundant in patients with COVID-19 (20.4% down, 4.6% up, 75% unchanged). Platelets from COVID-19 patients showed decreased levels of membrane plasmalogens, and a distinct decrease of long-chain, unsaturated triacylglycerols. Conversely, platelets from patients with COVID-19 displayed class-wide higher abundances of bis(monoacylglycero)phosphate and its biosynthetic precursor lysophosphatidylglycerol. Levels of these classes positively correlated with ex vivo platelet reactivity-as measured by P-selectin expression after PAR1 activation-irrespective of disease state. Conclusion Taken together, this investigation provides the first exploration of the profound impact of infection on the human platelet lipidome, and reveals associations between the lipid composition of platelets and their reactivity. These results warrant further lipidomic research in other infections and disease states involving platelet pathophysiology.

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