Abstract
Summary. Virus-induced coagulopathy is a typical example of the tight connection between inflammation and thrombosis. These two reactions are linked by pro-inflammatory agents, generated by activated neutrophils and their neutrophil extracellular traps (NETs). Extracellular membrane nanobubbles (EMNs), formed by a wide variety of cell types, have recently been identified as new entrants that play a key role in coagulopathy. EMNs directly and indirectly activate coagulation systems that lead to the further upregulation of inflammation and life-threatening organ dysfunction and thrombosis. EMNs are known to be responsible for the secretion, exchange, and transmission of important active biomolecules in COVID-19. Indeed, EMNs represent an essential mech- anism in intercellular communication, and the roles of EMNs in infection and thrombosis have been increasingly recognized. The extracellular microvesicles of viruses, virosomes, represent a new type of infectious agents, which determines new therapeutic goals in solving the problems of controlling viral infections. Understanding the biological nature of all these microvesicles when studying them in vivo is of paramount importance for the development of diagnostic and therapeutic methods.
References:
- Ahmed S., Zimba O., Gasparyan A. Yu. Thrombosis in coronavirus disease 2019 (COVID-19) through the prism of Virchow’s triad. Clin Rheumatol. 2020;39(9):2529–43. DOI: 10.1007/s10067–020–05275–1.
- Ackermann M., Verleden S.E., Kuehnel M. et al. Pulmonary vas- cular endothelialitis, thrombosis, and angiogenesis in Covid-19. N Engl J Med. 2020;383(2):120–8. doi: 10.1056/NEJMoa2015432.
- Starshinova A.A., Kushnareva E.A., Malkova A.M. et al. New coro- naviral infection: features of clinical course, capabilities of diag- nostics, treatment and prevention in adults and children. Voprosy sovremennoj pediatrii. 2020;19(2):123–31. (In Russ.). DOI: 10.15690/ v19i2.2105.
- Raeven P., Zipperle J., Drechsler S. Extracellular vesicles as mark- ers and mediators in sepsis. Theranostics. 2018;8(12):3348–65. DOI: 7150/thno.23453.
- Lusta K. A., Kondashevskaya M. V. Bacterial quter membrane nanovesicles: involment in pathogenesis (literature review). Vest- nik novyh medicinskih tekhnologij. 2019;(2):148–57. (In Russ.). DOI: 24411/2075–4094–2019–16306.
- Lai F.W., Lichty B.D., Bowdish D.M. Microvesicles: ubiquitous con- tributors to infection and immunity. J Leukoc Biol. 2015;97(2):237– DOI: 10.1189/jlb.3RU0513–292RR.
- LandaS.B., FilatovM.V., ArutyunianA.V. Research in exosomes secreting to different normal and tending to become malig- nant in vitro and in vivo cells. Kreativnaya hirurgiya i onkologiya. 2010;(4):79–82. (In Russ.).
- Nazimek K., Bryniarski K., Santocki M., Ptak W. Exosomes as medi- ators of intercellular communication: clinical implications. Pol Arch Med Wewn. 2015;125(5):370–80. DOI: 10.20452/pamw.2840.
- Zhang Y., Meng H., Ma R. et al. Circulating microparticles, blood cells, and endothelium induce procoagulant activity in sepsis through phosphatidylserine exposure. Shock. 2016;45(3):299–307. DOI: 10.1097/SHK.0000000000000509.
- Bashilov N.I., Tsybikov N.N., Kuznik B.I. The role of microparticles in conditions of norm and pathology. Uspekhi sovremennoj biologii. 2017;137(6):553–5. (In Russ.). DOI: 10.7868/S0042132417060035.
- Nehls J., Businger R., Hoffmann M. et al. Release of immuno- modulatory Ebola virus glycoprotein-containing microvesicles is suppressed by Tetherin in a species-specific manner. Cell Rep. 2019;26(7):1841–53.e6. DOI: 10.1016/j.celrep.2019.01.065.
- Bello-Morales R., Praena B., Nuez C. et al. Role of microvesicles in the spread of Herpes Simplex virus 1 in oligodendrocytic cells. J Virol. 2018;92(10): e00088–18. DOI: 10.1128/JVI.00088–18.
- Iba T., Ogura H. Role of extracellular vesicles in the development of sepsis-induced coagulopathy. J Intensive Care. 2018;6:68. DOI:10.1186/s40560–018–0340–6.
- Colafrancesco S., Alessandri C., Conti F., Priori R. COVID-19 gone
bad: A new character in the spectrum of the hyperferritinemic syndrome? Autoimmun Rev. 2020;19(7):102573. DOI: 10.1016/j. autrev.2020.102573.
- Iba T., Levy J.H. Inflammation and thrombosis: roles of neutrophils, platelets and endothelial cells and their interactions in throm- bus formation during sepsis. J Thromb Haemost. 2017;16(2):231– 41. DOI: 10.1111/jth.13911.
- Hellum M., Øvstebø R., Brusletto B.S. et al. Microparticle-associ- ated tissue factor activity correlates with plasma levels of bacte- rial lipopolysaccharides in meningococcal septic shock. Thromb Res. 2014;133(3):507–14. DOI: 10.1016/j.thromres.2013.12.031.
- KuznikB.I., SturovV.G., Levshin N. Yu. et al. Hemorrhagic and thrombotic diseases and syndromes in children and adolescents. Pathogenesis, clinic, diagnosis, therapy and prevention. Novosi- birsk: Nauka, 2018. 524 pp. (In Russ.).
- Gritsenko T.A., Kosyakova Yu.A., Davydkin I.L. et al. Blood dis- eases in outpatient practice. Ed. I.L. Davydkin. Moscow: GEO- TAR-Media, 2020. 272 pp. (In Russ.). DOI: 10/33029/9704–5916– 4-NEM-2020–1–272.
- Saheera S., PotnuriA.G., Krishnamurthy P. Nano-vesicle (mis) communication in senescence-related pathologies. Cells. 2020;9(9):1974. DOI: 10.3390/cells9091974.
- Brinkmann V., Laube B., Abu Abed U. et al. Neutrophil extra- cellular traps: how to generate and visualize them. J Vis Exp. 2010;(36):1724. DOI: 10.3791/1724.
- Tomar B., Anders H-J., Desai J., Mulay S.R. Neutrophils and neu- trophil extracellular traps drive necroinflammation in COVID-19. Cells. 2020;9(6):1383. DOI: 10.3390/cells9061383.
- Bonaventura A., Liberale L., Carbone F. et al. the pathophysi- ological role of neutrophil extracellular traps in inflammatory diseases. Thromb Haemost. 2018;118(1):6–27. DOI: 10.1160/TH17– 09–0630.
- Chatterjee V., Yang X., Ma Y. et al. Endothelial microvesicles car- rying Src-rich cargo impair adherens junction integrity and cyto- skeleton homeostasis. Cardiovasc Res. 2020;116(8):1525–38. DOI: 10.1093/cvr/cvz238.
- Kuznik B.I. Cytokines and hemostasis. I. Cytokines and vascular- platelet hemostasis. Tromboz, gemostaz i reologiya. 2012;(2):12– 23. (In Russ.).
- Boisrame-Helms J., Delabranche X., Degirmenci S.E. et al. Phar- macological modulation of procoagulant microparticles improves haemodynamic dysfunction during septic shock in rats. Thromb Haemost. 2014;111(1):154–64. DOI: 10.1160/TH13–04–0313.
- Helms J., Clere-Jehl R., Bianchini E. et al. Thrombomodulin favors leukocyte microvesicle fibrinolytic activity, reduces NETosis and prevents septic shock-induced coagulopathy in rats. Ann Intensive Care. 2017;7(1):118. DOI: 10.1186/s13613–017–0340-z.
