Differential contribution of various adhesion molecules to leukocyte kinetics in pulmonary microvessels of hyperoxia-exposed rat lungs
Autor: | Makoto Suematsu, Kazumi Nishio, Harukuni Tsumura, Kazuhiro Yamaguchi, Hiroyasu Kudo, Takuya Aoki, Yukio Suzuki, Katsuhiko Naoki, Koichi Suzuki, Hiroshi Serizawa, Atsushi Miyata, Shigeaki Moro-oka, Nagato Sato, Yuzuru Ishimura |
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Rok vydání: | 1998 |
Předmět: |
Pulmonary and Respiratory Medicine
Pathology medicine.medical_specialty Pulmonary Circulation P-selectin Intercellular Adhesion Molecule-1 Biology Hyperoxia In Vitro Techniques Critical Care and Intensive Care Medicine Blood cell Rats Sprague-Dawley medicine Leukocytes Animals Lung Cell adhesion molecule Microcirculation Hemodynamics Adhesion Rats Pulmonary Alveoli Red blood cell Kinetics P-Selectin medicine.anatomical_structure Biophysics Endothelium Vascular medicine.symptom Cell Adhesion Molecules |
Zdroj: | American journal of respiratory and critical care medicine. 157(2) |
ISSN: | 1073-449X |
Popis: | To elucidate the differential role of various adhesion molecules in distorting leukocyte behavior in the microvasculature of hyperoxia-exposed rat lungs, we investigated fluorescein-labeled leukocyte and erythrocyte kinetics in isolated lungs taken from the animals exposed to 90% O2 for 48 h under conditions in which endothelial intercellular adhesion molecule-1 (ICAM-1) and P-selectin were inhibited by appropriate monoclonal antibodies (1A29 for ICAM-1 and ARP2-4 for P-selectin), while leukocyte L-selectin was restrained with fucoidin. Measurements of blood cell kinetics were made by a confocal laser luminescence microscope coupled with a high-speed video camera. In addition, we histologically examined leukocyte accumulation within the alveolar septa and ICAM-1 as well as P-selectin expressions in the lung. We found that P-selectin expression was sparsely enhanced only in arterioles, whereas ICAM-1 was significantly induced in both venules and capillaries. Firm adhesion of leukocytes was not identified in arterioles and venules, whereas leukocyte rolling was evident in both the vessels. Arteriolar rolling was regulated via a P-selectin- and ICAM-1-independent but L-selectin-dependent mechanism, whereas venular rolling was mediated via a P-selectin-independent but ICAM-1- and L-selectin-dependent pathway. Leukocyte sequestration within capillaries was augmented by an ICAM-1-related mechanism. These findings may suggest that, in hyperoxia-exposed lungs, induction of adhesion molecules and their obstacles to leukocyte behavior are qualitatively different among arterioles, venules, and capillaries. |
Databáze: | OpenAIRE |
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