Cutting Edge: Role of MASP-3 in the Physiological Activation of Factor D of the Alternative Complement Pathway

J Immunol. 2019 Sep 15;203(6):1411-1416. doi: 10.4049/jimmunol.1900605. Epub 2019 Aug 9.

Abstract

The complement system, a part of the innate immune system, can be activated via three different pathways. In the alternative pathway, a factor D (FD) plays essential roles in both the initiation and the amplification loop and circulates as an active form. Mannose-binding lectin-associated serine proteases (MASPs) are key enzymes of the lectin pathway, and MASP-1 and/or MASP-3 are reported to be involved in the activation of FD. In the current study, we generated mice monospecifically deficient for MASP-1 or MASP-3 and found that the sera of the MASP-1-deficient mice lacked lectin pathway activity, but those of the MASP-3-deficient mice lacked alternative pathway activity with a zymogen FD. Furthermore, the results indicate that MASP-3 but not MASP-1 activates the zymogen FD under physiological conditions and MASP-3 circulates predominantly as an active form. Therefore, our study illustrates that, in mice, MASP-3 orchestrates the overall complement reaction through the activation of FD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Complement Activation / immunology
  • Complement Factor D / immunology*
  • Complement Pathway, Alternative / immunology*
  • Complement Pathway, Mannose-Binding Lectin / immunology
  • Complement System Proteins / immunology*
  • Female
  • Immune System / immunology
  • Lectins / immunology
  • Mannose-Binding Protein-Associated Serine Proteases / immunology*
  • Mice
  • Mice, Inbred C57BL

Substances

  • Lectins
  • Complement System Proteins
  • MASP-3 protein, mouse
  • Mannose-Binding Protein-Associated Serine Proteases
  • Complement Factor D