Thromb Haemost 2015; 114(05): 982-993
DOI: 10.1160/TH14-11-0951
Cellular Haemostasis and Platelets
Schattauer GmbH

Poly (I:C) downregulates platelet production and function through type I interferon

Leonardo Rivadeneyra
1   Laboratory of Experimental Thrombosis, Institute of Experimental Medicine-CONICET, National Academy of Medicine, Buenos Aires, Argentina
,
Roberto Gabriel Pozner
1   Laboratory of Experimental Thrombosis, Institute of Experimental Medicine-CONICET, National Academy of Medicine, Buenos Aires, Argentina
,
Roberto Meiss
2   Department of Pathology, Institute of Oncological Research, National Academy of Medicine, Buenos Aires, Argentina
,
Carlos Fondevila
3   Bazterrica Clinic, Buenos Aires, Argentina
,
Ricardo Martin Gómez
4   Biotechnology and Molecular Biology Institute, CONICET-UNLP, La Plata, Argentina
,
Mirta Schattner
1   Laboratory of Experimental Thrombosis, Institute of Experimental Medicine-CONICET, National Academy of Medicine, Buenos Aires, Argentina
› Author Affiliations

Financial support: This study was supported by Grants from ANPCyT PICT 2010/0411, PIP 114/200801/00603 from RGP, ANPCyT PICT 2012/0434 (RMG) and ANPCyT PICTOGSK 2011/009 and PICT 2011/0733 from MS.
Further Information

Publication History

Received: 17 November 2014

Accepted after major revision: 24 May 2015

Publication Date:
06 December 2017 (online)

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Summary

Thrombocytopenia is a frequent complication of viral infections; the underlying mechanisms appear to depend on the identity of the virus involved. Previous research, including reports from our group, indicates that as well as having antiviral activity type I interferons (IFN I) selectively downregulate platelet production. In this study we extended understanding of the role of endogenous IFN I in megakaryo/ thrombopoiesis by evaluating platelet and megakaryocyte physiology in mice treated with polyinosinic:polycytidylic acid [poly (I:C)], a synthetic analogue of double-stranded RNA, Toll-like receptor-3 ligand and strong IFNp inducer. Mice-treated with poly (I:C) showed thrombocytopaenia, an increase in mean platelet volume and abnormal haemostatic and inflammatory platelet-mediated functionality, indicated by decreased fibrinogen binding and platelet adhesion, prolonged tail bleeding times and impaired P-Selectin externalisation, RANTES release and thrombin-induced platelet-neutrophil aggregate formation. These changes were associated with an increase in size and an abnormal distribution of bone marrow megakaryocytes within the vascular niche and were directly correlated with the plasmatic and bone marrow IFNp levels. All these effects were absent in genetically modified mice lacking the IFN I receptor. Our results suggest that IFN I is the central mediator of poly (I:C)-induced thrombocytopenia and platelet dysfunction and indicate that these abnormalities are due to changes in the last stages of megakaryocyte development. These data provide new evidence for the role of IFN I in megakaryocyte distribution in the bone marrow niches and its influence on thrombopoiesis and haemostasis.