Phagocytosis of apoptotic eosinophils but not neutrophils by bronchial epithelial cells

Summary Background We have previously demonstrated that human bronchial epithelial cells engulf apoptotic eosinophils. Objectives To compare and contrast the phagocytic capabilities of monocyte‐derived macrophage and primary airway epithelial cells for apoptotic granulocytes. Results Here we compare...

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Veröffentlicht in:Clinical and experimental allergy 2004-10, Vol.34 (10), p.1514-1524
Hauptverfasser: Sexton, D. W., Al-Rabia, M., Blaylock, M. G., Walsh, G. M.
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container_issue 10
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Al-Rabia, M.
Blaylock, M. G.
Walsh, G. M.
description Summary Background We have previously demonstrated that human bronchial epithelial cells engulf apoptotic eosinophils. Objectives To compare and contrast the phagocytic capabilities of monocyte‐derived macrophage and primary airway epithelial cells for apoptotic granulocytes. Results Here we compared phagocytosis of human apoptotic eosinophils and neutrophils by small and large airway epithelial cells (SAEC and LAEC) and monocyte‐derived macrophages. Confocal microscopy of F‐actin staining and scanning and transmission electron microscopy revealed phagocytic cup formation around apoptotic eosinophils by airway epithelial cells (AEC) membranes with evidence of their digestion. Resting and cytokine‐stimulated AEC did not recognize and ingest apoptotic neutrophils. The latter were phagocytosed by macrophages that exhibited greater ingestion of and higher capacity for, apoptotic eosinophils over apoptotic neutrophils. Cytochalasin D completely abolished uptake of apoptotic eosinophils by SAEC, LAEC or macrophage monolayers. Ligation of epithelial cell CD44 receptors for 24 h increased phagocytosis of apoptotic eosinophils by SAEC and LAEC with a potency comparable with that of IL‐1. Phagocytosis was a specific receptor‐mediated process involving integrin‐ (αvβ3, αvβ5, CD36), phosphatidylserine receptor‐ and lectin‐dependent mechanisms. No significant differences were observed in avarice for apoptotic eosinophils by SAEC or LAEC either resting, CD44 monoclonal antibodies‐ or cytokine‐ stimulated, or in their usage and expression of recognition receptors. Conclusion These findings further suggest and define an important role for the bronchial epithelium in the selective removal of apoptotic eosinophils from the airways in asthma.
doi_str_mv 10.1111/j.1365-2222.2004.02054.x
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The latter were phagocytosed by macrophages that exhibited greater ingestion of and higher capacity for, apoptotic eosinophils over apoptotic neutrophils. Cytochalasin D completely abolished uptake of apoptotic eosinophils by SAEC, LAEC or macrophage monolayers. Ligation of epithelial cell CD44 receptors for 24 h increased phagocytosis of apoptotic eosinophils by SAEC and LAEC with a potency comparable with that of IL‐1. Phagocytosis was a specific receptor‐mediated process involving integrin‐ (αvβ3, αvβ5, CD36), phosphatidylserine receptor‐ and lectin‐dependent mechanisms. No significant differences were observed in avarice for apoptotic eosinophils by SAEC or LAEC either resting, CD44 monoclonal antibodies‐ or cytokine‐ stimulated, or in their usage and expression of recognition receptors. 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W.</creatorcontrib><creatorcontrib>Al-Rabia, M.</creatorcontrib><creatorcontrib>Blaylock, M. G.</creatorcontrib><creatorcontrib>Walsh, G. M.</creatorcontrib><title>Phagocytosis of apoptotic eosinophils but not neutrophils by bronchial epithelial cells</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Summary Background We have previously demonstrated that human bronchial epithelial cells engulf apoptotic eosinophils. Objectives To compare and contrast the phagocytic capabilities of monocyte‐derived macrophage and primary airway epithelial cells for apoptotic granulocytes. Results Here we compared phagocytosis of human apoptotic eosinophils and neutrophils by small and large airway epithelial cells (SAEC and LAEC) and monocyte‐derived macrophages. Confocal microscopy of F‐actin staining and scanning and transmission electron microscopy revealed phagocytic cup formation around apoptotic eosinophils by airway epithelial cells (AEC) membranes with evidence of their digestion. Resting and cytokine‐stimulated AEC did not recognize and ingest apoptotic neutrophils. The latter were phagocytosed by macrophages that exhibited greater ingestion of and higher capacity for, apoptotic eosinophils over apoptotic neutrophils. Cytochalasin D completely abolished uptake of apoptotic eosinophils by SAEC, LAEC or macrophage monolayers. Ligation of epithelial cell CD44 receptors for 24 h increased phagocytosis of apoptotic eosinophils by SAEC and LAEC with a potency comparable with that of IL‐1. Phagocytosis was a specific receptor‐mediated process involving integrin‐ (αvβ3, αvβ5, CD36), phosphatidylserine receptor‐ and lectin‐dependent mechanisms. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phagocytosis of apoptotic eosinophils but not neutrophils by bronchial epithelial cells</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2004-10</date><risdate>2004</risdate><volume>34</volume><issue>10</issue><spage>1514</spage><epage>1524</epage><pages>1514-1524</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Summary Background We have previously demonstrated that human bronchial epithelial cells engulf apoptotic eosinophils. Objectives To compare and contrast the phagocytic capabilities of monocyte‐derived macrophage and primary airway epithelial cells for apoptotic granulocytes. Results Here we compared phagocytosis of human apoptotic eosinophils and neutrophils by small and large airway epithelial cells (SAEC and LAEC) and monocyte‐derived macrophages. Confocal microscopy of F‐actin staining and scanning and transmission electron microscopy revealed phagocytic cup formation around apoptotic eosinophils by airway epithelial cells (AEC) membranes with evidence of their digestion. Resting and cytokine‐stimulated AEC did not recognize and ingest apoptotic neutrophils. The latter were phagocytosed by macrophages that exhibited greater ingestion of and higher capacity for, apoptotic eosinophils over apoptotic neutrophils. Cytochalasin D completely abolished uptake of apoptotic eosinophils by SAEC, LAEC or macrophage monolayers. Ligation of epithelial cell CD44 receptors for 24 h increased phagocytosis of apoptotic eosinophils by SAEC and LAEC with a potency comparable with that of IL‐1. Phagocytosis was a specific receptor‐mediated process involving integrin‐ (αvβ3, αvβ5, CD36), phosphatidylserine receptor‐ and lectin‐dependent mechanisms. No significant differences were observed in avarice for apoptotic eosinophils by SAEC or LAEC either resting, CD44 monoclonal antibodies‐ or cytokine‐ stimulated, or in their usage and expression of recognition receptors. Conclusion These findings further suggest and define an important role for the bronchial epithelium in the selective removal of apoptotic eosinophils from the airways in asthma.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15479265</pmid><doi>10.1111/j.1365-2222.2004.02054.x</doi><tpages>11</tpages></addata></record>
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subjects Allergic diseases
Apoptosis - physiology
apoptotic eosinophils
apoptotic neutrophils
Biological and medical sciences
Bronchi - immunology
Bronchi - physiology
Cells, Cultured
Eosinophils - physiology
epithelial cells
Epithelial Cells - immunology
Epithelial Cells - physiology
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Hyaluronan Receptors - immunology
Immunopathology
Integrins - physiology
Interleukin-1 - immunology
Jumonji Domain-Containing Histone Demethylases
Lectins - physiology
macrophage
Macrophages - physiology
Medical sciences
Microscopy, Confocal - methods
Microscopy, Electron - methods
Microscopy, Electron, Scanning - methods
Neutrophils - physiology
phagocytosis
Phagocytosis - physiology
Receptors, Cell Surface - physiology
title Phagocytosis of apoptotic eosinophils but not neutrophils by bronchial epithelial cells
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