Erythrocyte-derived microvesicles amplify systemic inflammation by thrombin-dependent activation of complement

Arteriosclerosis, Thrombosis, and Vascular Biology

Volumn 34, Issue 2, 2014, Pages 313-320

  Zecher, Daniel ^a   Cumpelik, Arun ^a   Schifferli, Jürg A ^a  

^a UNIVERSITY HOSPITAL BASEL   (Switzerland)

Author keywords

blood coagulation; blood component transfusion; cell derived microparticles; complement system proteins; inflammation

Indexed keywords

BLOOD COAGULATION; BLOOD COMPONENT TRANSFUSION; CELL-DERIVED MICROPARTICLES; COMPLEMENT SYSTEM PROTEINS; INFLAMMATION;

ANIMALS; CELL-DERIVED MICROPARTICLES; COMPLEMENT ACTIVATION; COMPLEMENT C3; ERYTHROCYTE TRANSFUSION; ERYTHROCYTES; GENOTYPE; INFLAMMATION; LEUKOPENIA; LIPOPOLYSACCHARIDES; LIPOSOMES; LUNG; MICE; MICE, 129 STRAIN; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, KNOCKOUT; MODELS, ANIMAL; NEUTROPHIL INFILTRATION; PEPTIDE FRAGMENTS; PHENOTYPE; PHOSPHATIDYLSERINES; RECEPTOR, ANAPHYLATOXIN C5A; THROMBIN; TIME FACTORS;

EID: 84894994184     PISSN: 10795642     EISSN: 15244636     Source Type: Journal    
DOI: 10.1161/ATVBAHA.113.302378     Document Type: Article

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