Macrophage IL-1β promotes arteriogenesis by autocrine STAT3- and NF-κB-mediated transcription of pro-angiogenic VEGF-A

Cell Rep. 2022 Feb 1;38(5):110309. doi: 10.1016/j.celrep.2022.110309.

Abstract

Peripheral artery disease (PAD) leads to considerable morbidity, yet strategies for therapeutic angiogenesis fall short of being impactful. Inflammatory macrophage subsets play an important role in orchestrating post-developmental angiogenesis, but the underlying mechanisms are unclear. Here, we find that macrophage VEGF-A expression is dependent upon the potent inflammatory cytokine, IL-1β. IL-1β promotes pro-angiogenic VEGF-A165a isoform transcription via activation and promoter binding of STAT3 and NF-κB, as demonstrated by gene-deletion, gain-of-function, inhibition, and chromatin immunoprecipitation assays. Conversely, IL-1β-deletion or inhibition of STAT3 or NF-κB increases anti-angiogenic VEGF-A165b isoform expression, indicating IL-1β signaling may also direct splice variant selection. In an experimental PAD model of acute limb ischemia, macrophage IL-1β expression is required for pro-angiogenic VEGF-A expression and for VEGF-A-induced blood flow recovery via angio- or arteriogenesis. Though further study is needed, macrophage IL-1β-dependent transcription of VEGF-A via STAT3 and NF-κB may have potential to therapeutically promote angiogenesis in the setting of PAD.

Keywords: NF-κB; STAT3; VEGF-A; angiogenesis; hindlimb ischemiahindlimb; inflammation; interleukin-1; macrophage; peripheral artery disease; vascular biology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cytokines / metabolism
  • DNA-Binding Proteins / metabolism
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism*
  • Macrophages / metabolism*
  • Mice, Transgenic
  • NF-kappa B / metabolism*
  • Promoter Regions, Genetic / genetics
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*
  • Trans-Activators / metabolism
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Cytokines
  • DNA-Binding Proteins
  • IL1B protein, mouse
  • Interleukin-1beta
  • NF-kappa B
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Trans-Activators
  • Vascular Endothelial Growth Factor A