Limb functional recovery is impaired in fibroblast growth factor-2 (FGF2) deficient mice despite chronic ischaemia-induced vascular growth

Growth Factors. 2020 Feb;38(2):75-93. doi: 10.1080/08977194.2020.1767612. Epub 2020 Jun 4.

Abstract

FGF2 is a potent stimulator of vascular growth; however, even with a deficiency of FGF2 (Fgf2-/-), developmental vessel growth or ischaemia-induced revascularization still transpires. It remains to be elucidated as to what function, if any, FGF2 has during ischaemic injury. Wildtype (WT) or Fgf2-/- mice were subjected to hindlimb ischaemia for up to 42 days. Limb function, vascular growth, inflammatory- and angiogenesis-related proteins, and inflammatory cell infiltration were assessed in sham and ischaemic limbs at various timepoints. Recovery of ischaemic limb function was delayed in Fgf2-/- mice. Yet, vascular growth response to ischaemia was similar between WT and Fgf2-/- hindlimbs. Several angiogenesis- and inflammatory-related proteins (MCP-1, CXCL16, MMPs and PAI-1) were increased in Fgf2-/- ischaemic muscle. Neutrophil or monocyte recruitment/infiltration was elevated in Fgf2-/- ischaemic muscle. In summary, our study indicates that loss of FGF2 induces a pro-inflammatory microenvironment in skeletal muscle which exacerbates ischaemic injury and delays functional limb use.

Keywords: Fibroblast growth factor 2; angiogenesis; arteriogenesis; hindlimb ischaemia; inflammation; micro-CT.

Publication types

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

MeSH terms

  • Animals
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism
  • Chemokine CXCL16 / genetics
  • Chemokine CXCL16 / metabolism
  • Fibroblast Growth Factor 2 / genetics
  • Fibroblast Growth Factor 2 / metabolism*
  • Hindlimb / blood supply
  • Matrix Metalloproteinases / genetics
  • Matrix Metalloproteinases / metabolism
  • Mice
  • Muscle, Skeletal / blood supply
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / physiology
  • Neovascularization, Physiologic*
  • Plasminogen Activator Inhibitor 1 / genetics
  • Plasminogen Activator Inhibitor 1 / metabolism
  • Regeneration
  • Reperfusion Injury / metabolism*

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Chemokine CXCL16
  • Cxcl16 protein, mouse
  • Plasminogen Activator Inhibitor 1
  • Fibroblast Growth Factor 2
  • Matrix Metalloproteinases