Platelets Disseminate Extracellular Vesicles in Lymph in Rheumatoid Arthritis
Author(s) -
Nicolas Tessandier,
Imène Melki,
Nathalie Cloutier,
Isabelle Allaeys,
Adam Miszta,
Sisareuth Tan,
Andreea Milasan,
Sara Michel,
Abderrahim Benmoussa,
Tania Lévesque,
Francine Côté,
Steven E. McKenzie,
Caroline Gilbert,
Patrick Provost,
Alain Brisson,
Alisa S. Wolberg,
Paul R. Fortin,
Catherine Martel,
Éric Boilard
Publication year - 2020
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.119.313698
Subject(s) - lymph , platelet , lymphatic system , immunology , inflammation , platelet activation , rheumatoid arthritis , arthritis , medicine , pathology , fibrin , immune system , synovial fluid , osteoarthritis , alternative medicine
Objective: The lymphatic system is a circulatory system that unidirectionally drains the interstitial tissue fluid back to blood circulation. Although lymph is utilized by leukocytes for immune surveillance, it remains inaccessible to platelets and erythrocytes. Activated cells release submicron extracellular vesicles (EV) that transport molecules from the donor cell. In rheumatoid arthritis, EV accumulate in the joint where they can interact with numerous cellular lineages. However, whether EV can exit the inflamed tissue to recirculate is unknown. Here, we investigated whether vascular leakage that occurs during inflammation could favor EV access to the lymphatic system. Approach and Results: Using an in vivo model of autoimmune inflammatory arthritis, we show that there is an influx of platelet EV, but not EV from erythrocytes or leukocytes, in joint-draining lymph. In contrast to blood platelet EV, lymph platelet EV lacked mitochondrial organelles and failed to promote coagulation. Platelet EV influx in lymph was consistent with joint vascular leakage and implicated the fibrinogen receptor α2bβ3 and platelet-derived serotonin.Conclusions: These findings show that platelets can disseminate their EV in fluid that is inaccessible to platelets and beyond the joint in this disease.
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