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fMLP-stimulated release of reactive oxygen species from adherent leukocytes increases microvessel permeability

Department of Physiology and Pharmacology, West Virginia University, Morgantown, West Virginia

Submitted 25 April 2005 ; accepted in final form 17 August 2005

Our previous study (Am J Physiol Heart Circ Physiol 288: H1331–H1338, 2005) demonstrated that TNF- induced significant leukocyte adhesion without causing increases in microvessel permeability, and that formyl-Met-Leu-Phe-OH (fMLP)-stimulated neutrophils in the absence of adhesion increased microvessel permeability via released reactive oxygen species (ROS). The objective of our present study is to investigate the mechanisms that regulate neutrophil respiratory burst and the roles of fMLP-stimulated ROS release from adherent leukocytes in microvessel permeability. A technique that combines single-microvessel perfusion with autologous blood perfusion was employed in venular microvessels of rat mesenteries. Leukocyte adhesion was induced by systemic application of TNF-. Microvessel permeability was assessed by measuring hydraulic conductivity (L_p). The 2-h autologous blood perfusion after TNF- application increased leukocyte adhesion from 1.2 ± 0.2 to 13.3 ± 1.6 per 100 µm of vessel length without causing increases in L_p. When fMLP (10 µM) was applied to either perfusate (n = 5) or superfusate (n = 8) in the presence of adherent leukocytes, L_p transiently increased to 4.9 ± 0.9 and 4.4 ± 0.3 times the control value, respectively. Application of superoxide dismutase or an iron chelator, deferoxamine mesylate, after fMLP application prevented or attenuated the L_p increase. Chemiluminescence measurements in isolated neutrophils demonstrated that TNF- alone did not induce ROS release but that preexposure of neutrophils to TNF- in vivo or in vitro potentiated fMLP-stimulated ROS release. These results suggest a priming role of TNF- in fMLP-stimulated neutrophil respiratory burst and indicate that the released ROS play a key role in leukocyte-mediated permeability increases during acute inflammation.

formyl-Met-Leu-Phe-OH; hydraulic conductivity; neutrophil priming

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