Targeted deletion of the inhibitory NF-kappaB p50 subunit in bone marrow-derived cells improves collateral growth after arterial occlusion

Cardiovasc Res. 2010 Oct 1;88(1):179-85. doi: 10.1093/cvr/cvq150. Epub 2010 May 21.

Abstract

Aims: Adaptive collateral artery growth (arteriogenesis) is an important mechanism to maintain tissue perfusion upon arterial obstruction. Leucocytes and inflammatory mediators play a crucial role in this process. Depletion of the nuclear factor kappa B (NF-κB) p50 subunit modulates inflammatory processes in cardiovascular disease. We hypothesized that NF-κB p50 is a regulator of the inflammatory response after arterial occlusion and subsequent collateral perfusion.

Methods and results: Unilateral femoral artery ligation was performed in NF-κB p50-/- and wild-type (Wt, B6/129PF2) mice. Seven days after arterial occlusion, tissue perfusion restoration was significantly enhanced in NF-κB p50-/- mice compared with Wt mice (42.9 ± 3.9 vs. 32.0 ± 2.6% perfusion recovery, P = 0.04). Transplantation of NF-κB p50-/- bone marrow (bm) into Wt mice and vice versa showed that the effect of p50 subunit depletion can be predominantly attributed to the bone marrow-derived circulating cells (NF-κB p50-/- bm in Wt mice 42.1 ± 1.5%, Wt bm in NF-κB p50-/- mice 35.4±1.5% perfusion recovery). Histological analyses revealed a more elaborate extravasation of monocytes in hindlimb tissue of NF-κB p50-/- mice. Chemotaxis assays confirmed the increased migration ability of NF-κB p50-/- monocytes, which may be due to an observed increased integrin expression. Upon stimulation of blood from NF-κB p50-/- and Wt mice more interleukin-6 was produced, confirming the pro-inflammatory phenotype in absence of the p50 subunit.

Conclusion: Depletion of the NF-κB p50 subunit enhances collateral artery growth. Its absence in circulating cells improves tissue perfusion restoration after femoral artery ligation by increasing macrophage influx into the growing collateral vessels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arterial Occlusive Diseases / genetics
  • Arterial Occlusive Diseases / immunology*
  • Arterial Occlusive Diseases / physiopathology
  • Bone Marrow Cells / immunology*
  • Bone Marrow Transplantation
  • Chemotaxis, Leukocyte
  • Collateral Circulation*
  • Disease Models, Animal
  • Female
  • Femoral Artery / surgery
  • Gene Deletion*
  • Inflammation Mediators / blood
  • Interleukin-6 / blood
  • Ligation
  • Macrophages / immunology
  • Male
  • Mice
  • Mice, Knockout
  • Monocytes / immunology
  • NF-kappa B p50 Subunit / deficiency*
  • NF-kappa B p50 Subunit / genetics
  • Neovascularization, Physiologic*
  • Time Factors

Substances

  • Inflammation Mediators
  • Interleukin-6
  • NF-kappa B p50 Subunit