Simultaneous activation of complement and coagulation by MBL-associated serine protease 2

• Published in: PloS one Vol. 2; no. 7; p. e623
• Main Authors: Krarup, Anders, Wallis, Russell, Presanis, Julia S, Gál, Péter, Sim, Robert B
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 18.07.2007; Public Library of Science (PLoS)
• Subjects: Animals; Bacteria; Biochemistry; Biochemistry/Macromolecular Chemistry; Blood Coagulation - genetics; Blood Coagulation - physiology; Clotting; Coagulation; Coagulation factors; Complement; Complement activation; Complement Activation - physiology; Complement component C2; Complement component C4; Cricetinae; Crosslinking; Enzymes; Factor Xa - genetics; Factor Xa - metabolism; Factor XIII - metabolism; Fibrin; Fibrin - metabolism; Fibrinogen; Fibrinogen - metabolism; Foreign bodies; Hematology; Immune response; Immune system; Immunology; Immunology/Immunity to Infections; Immunology/Innate Immunity; Innate immunity; Invertebrates; Lectins; Mannan; Mannose-binding lectin; Mannose-Binding Lectin - metabolism; Mannose-Binding Protein-Associated Serine Proteases - genetics; Mannose-Binding Protein-Associated Serine Proteases - metabolism; MASP-2 protein; Membranes; Microorganisms; Pathogens; Peptide Fragments - metabolism; Polypeptides; Protease; Proteases; Proteins; Prothrombin; Prothrombin - genetics; Prothrombin - metabolism; Serine; Serine proteinase; Thrombin
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0000623

The complement system is an important immune mechanism mediating both recognition and elimination of foreign bodies. The lectin pathway is one pathway of three by which the complement system is activated. The characteristic protease of this pathway is Mannan-binding lectin (MBL)-associated serine protease 2 (MASP2), which cleaves complement proteins C2 and C4. We present a novel and alternative role of MASP2 in the innate immune system. We have shown that MASP2 is capable of promoting fibrinogen turnover by cleavage of prothrombin, generating thrombin. By using a truncated active form of MASP2 as well as full-length MASP2 in complex with MBL, we have shown that the thrombin generated is active and can cleave both factor XIII and fibrinogen, forming cross-linked fibrin. To explore the biological significance of these findings we showed that fibrin was covalently bound on a bacterial surface to which MBL/MASP2 complexes were bound. These findings suggest that, as has been proposed for invertebrates, limited clotting may contribute to the innate immune response.