Thromb Haemost 2017; 117(09): 1772-1781
DOI: 10.1160/TH17-03-0156
Cellular Haemostasis and Platelets
Schattauer GmbH

Triggering Receptor Expressed on Myeloid cells-1: a new player in platelet aggregation

Lucie Jolly
1   INSERM UMRS-1116, Faculté de Médecine Nancy, Université de Lorraine, Nancy, France
,
Jérémie Lemarié
1   INSERM UMRS-1116, Faculté de Médecine Nancy, Université de Lorraine, Nancy, France
2   CHU Nancy, Hôpital Central, Service de Réanimation Médicale, Nancy, France
,
Kevin Carrasco
1   INSERM UMRS-1116, Faculté de Médecine Nancy, Université de Lorraine, Nancy, France
,
Batric Popovic
1   INSERM UMRS-1116, Faculté de Médecine Nancy, Université de Lorraine, Nancy, France
3   CHU Nancy, Hôpital Brabois, Service de Cardiologie, Vandoeuvre-lès-Nancy, France
,
Marc Derive
4   INOTREM SA, Nancy, France
,
Amir Boufenzer
4   INOTREM SA, Nancy, France
,
Sébastien Gibot
1   INSERM UMRS-1116, Faculté de Médecine Nancy, Université de Lorraine, Nancy, France
2   CHU Nancy, Hôpital Central, Service de Réanimation Médicale, Nancy, France
› Author Affiliations
Further Information

Publication History

Received: 07 March 2017

Accepted after minor revision: 11 May 2017

Publication Date:
09 November 2017 (online)

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Summary

Triggering Receptor Expressed on Myeloid cells-1 (TREM-1) is an immunoreceptor initially known to be expressed on neutrophils and monocytes/macrophages. TREM-1 acts as an amplifier of the inflammatory response during both infectious and aseptic inflammatory diseases. Another member of the TREM family, The Triggering receptor expressed on myeloid cells Like Transcript-1 (TLT-1) is exclusively expressed in platelets and promotes platelet aggregation. As the gene that encodes for TLT-1 is located in the TREM-1 gene cluster, this prompted us to investigate the expression of TREM-1 on platelets. Here we show that TREM-1 is constitutively expressed in α-granules and mobilised at the membrane upon platelet activation. Pharmacologic inhibition of TREM-1 reduces platelet activation as well as platelet aggregation induced by collagen, ADP, and thrombin in human platelets. Aggregation is similarly impaired in platelets from Trem-1−/− mice. In vivo, TREM-1 inhibition decreases thrombus formation in a carotid artery model of thrombosis and protects mice during pulmonary embolism without excessive bleeding. These findings suggest that TREM-1 inhibition could be useful adducts in antiplatelet therapies.

Supplementary Material to this article is available online at www.thrombosis-online.com.