Alpha chemokines regulate direct lung ischemia-reperfusion injury

J Heart Lung Transplant. 2004 May;23(5):585-91. doi: 10.1016/S1053-2498(03)00300-0.

Abstract

Background: Alpha chemokines function predominantly to recruit and activate neutrophils, which are important effectors of acute lung injury. This study evaluated whether blockade of 2 potent alpha chemokines, macrophage inflammatory protein-2 (MIP-2) and cytokine-induced neutrophil chemoattractant (CINC), is protective against lung ischemia-reperfusion injury in a warm in situ hilar clamp model.

Methods: Left lungs of Long-Evans rats underwent normothermic ischemia for 90 minutes and reperfusion for up to 4 hours. Treated animals received antibodies to MIP-2 or CINC immediately prior to reperfusion. Lung injury was quantitated by vascular permeability to (125)I-radiolabeled bovine serum albumin, lung tissue neutrophil sequestration (myeloperoxidase [MPO] content), and alveolar leukocyte content in bronchoalveolar lavage (BAL) fluid. CINC and MIP-2 mRNA expression were assessed by northern blot, while ribonuclease protection assays were performed to evaluate mRNA expression for a number of early response cytokines. MIP-2 and CINC protein expression in injured lungs was determined by immunoblotting.

Results: Treatment with antibodies to CINC or MIP-2 was associated with significant protection against increases in vascular permeability, MPO content and alveolar leukocyte sequestration in injured lungs. Expression of CINC and MIP-2 mRNA peaked after 2 hours of reperfusion in injured lungs, and protein levels were evident on immunoblotting after 3 hours of reperfusion. Neither CINC nor MIP-2 blockade appeared to modulate cytokine mRNA expression.

Conclusions: CINC and MIP-2 are important mediators involved in direct lung ischemia-reperfusion injury. They appear to function by modulating neutrophil recruitment, but not inflammatory cytokine release.

MeSH terms

  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Bronchoalveolar Lavage
  • Capillary Permeability / physiology
  • Chemokine CXCL2
  • Chemokines, CXC / analysis
  • Chemokines, CXC / physiology*
  • Disease Models, Animal
  • Intercellular Signaling Peptides and Proteins / analysis
  • Intercellular Signaling Peptides and Proteins / physiology
  • Lung / blood supply*
  • Peroxidase / analysis
  • Rats
  • Rats, Long-Evans
  • Reperfusion Injury / physiopathology*

Substances

  • Chemokine CXCL2
  • Chemokines, CXC
  • Cxcl2 protein, rat
  • Intercellular Signaling Peptides and Proteins
  • Peroxidase