C3 Deficiency Leads to Increased Angiogenesis and Elevated Pro-Angiogenic Leukocyte Recruitment in Ischemic Muscle Tissue

Int J Mol Sci. 2021 May 28;22(11):5800. doi: 10.3390/ijms22115800.

Abstract

The complement system is a potent inflammatory trigger, activator, and chemoattractant for leukocytes, which play a crucial role in promoting angiogenesis. However, little information is available about the influence of the complement system on angiogenesis in ischemic muscle tissue. To address this topic and analyze the impact of the complement system on angiogenesis, we induced muscle ischemia in complement factor C3 deficient (C3-/-) and wildtype control mice by femoral artery ligation (FAL). At 24 h and 7 days after FAL, we isolated the ischemic gastrocnemius muscles and investigated them by means of (immuno-)histological analyses. C3-/- mice showed elevated ischemic damage 7 days after FAL, as evidenced by H&E staining. In addition, angiogenesis was increased in C3-/- mice, as demonstrated by increased capillary/muscle fiber ratio and increased proliferating endothelial cells (CD31+/BrdU+). Moreover, our results showed that the total number of leukocytes (CD45+) was increased in C3-/- mice, which was based on an increased number of neutrophils (MPO+), neutrophil extracellular trap formation (MPO+/CitH3+), and macrophages (CD68+) displaying a shift toward an anti-inflammatory and pro-angiogenic M2-like polarized phenotype (CD68+/MRC1+). In summary, we show that the deficiency of complement factor C3 increased neutrophil and M2-like polarized macrophage accumulation in ischemic muscle tissue, contributing to angiogenesis.

Keywords: C3; NETs; angiogenesis; complement system; ischemia; leukocytes; macrophage polarization; macrophages; neutrophil extracellular traps; neutrophils.

MeSH terms

  • Animals
  • Capillaries / metabolism
  • Capillaries / physiopathology*
  • Complement C3 / deficiency*
  • Complement C3 / genetics
  • Disease Models, Animal
  • Fluorescent Antibody Technique / methods
  • Humans
  • Ischemia / genetics
  • Ischemia / physiopathology*
  • Leukocytes / metabolism*
  • Macrophage Activation
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Skeletal / blood supply
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiopathology*
  • Neutrophil Infiltration
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism

Substances

  • Complement C3
  • Platelet Endothelial Cell Adhesion Molecule-1