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 |
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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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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.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/j.1365-2222.2004.02054.x</identifier><identifier>PMID: 15479265</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>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</subject><ispartof>Clinical and experimental allergy, 2004-10, Vol.34 (10), p.1514-1524</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Oct 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4914-a486b41549f1a81f83a3f4f857c3eea5dbe984e106ab9ae1cbe15f93d103c6ad3</citedby><cites>FETCH-LOGICAL-c4914-a486b41549f1a81f83a3f4f857c3eea5dbe984e106ab9ae1cbe15f93d103c6ad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2222.2004.02054.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2222.2004.02054.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16173515$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15479265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sexton, D. 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. 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.</description><subject>Allergic diseases</subject><subject>Apoptosis - physiology</subject><subject>apoptotic eosinophils</subject><subject>apoptotic neutrophils</subject><subject>Biological and medical sciences</subject><subject>Bronchi - immunology</subject><subject>Bronchi - physiology</subject><subject>Cells, Cultured</subject><subject>Eosinophils - physiology</subject><subject>epithelial cells</subject><subject>Epithelial Cells - immunology</subject><subject>Epithelial Cells - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Hyaluronan Receptors - immunology</subject><subject>Immunopathology</subject><subject>Integrins - physiology</subject><subject>Interleukin-1 - immunology</subject><subject>Jumonji Domain-Containing Histone Demethylases</subject><subject>Lectins - physiology</subject><subject>macrophage</subject><subject>Macrophages - physiology</subject><subject>Medical sciences</subject><subject>Microscopy, Confocal - methods</subject><subject>Microscopy, Electron - methods</subject><subject>Microscopy, Electron, Scanning - methods</subject><subject>Neutrophils - physiology</subject><subject>phagocytosis</subject><subject>Phagocytosis - physiology</subject><subject>Receptors, Cell Surface - physiology</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV9rFDEUxYModq1-BRkE-zZjMvkzyYMPZalVWGqFSh9DJnvjZp2djMkM7n57M-7agi96IeRy8zuXEw5CBcEVyfVuWxEqeFnnqmqMWYVrzFm1f4IWDw9P0QIrzspGKnaGXqS0xRhTruRzdEY4a1Qt-ALd327Mt2APY0g-FcEVZgjDGEZvC8ijPgwb36WincaiD_nANMY_s0PRxtDbjTddAYMfN9DNrYWuSy_RM2e6BK9O9zn6-uHqbvmxXH2-_rS8XJWWKcJKw6RoWbajHDGSOEkNdcxJ3lgKYPi6BSUZECxMqwwQ2wLhTtE1wdQKs6bn6OK4d4jhxwRp1DufZgemhzAlLYQSUtbqnyBpJMOSNRl88xe4DVPs8yc0UUrVVFKSIXmEbAwpRXB6iH5n4kETrOeI9FbPSeg5CT1HpH9HpPdZ-vq0f2p3sH4UnjLJwNsTYJI1nYumtz49coI0lJOZe3_kfvoODv9tQC-vLucu68uj3qcR9g96E79r0dCG6_ub6-zq9ou6a1b6hv4C5YC8IQ</recordid><startdate>200410</startdate><enddate>200410</enddate><creator>Sexton, D. W.</creator><creator>Al-Rabia, M.</creator><creator>Blaylock, M. G.</creator><creator>Walsh, G. M.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>200410</creationdate><title>Phagocytosis of apoptotic eosinophils but not neutrophils by bronchial epithelial cells</title><author>Sexton, D. W. ; Al-Rabia, M. ; Blaylock, M. G. ; Walsh, G. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4914-a486b41549f1a81f83a3f4f857c3eea5dbe984e106ab9ae1cbe15f93d103c6ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Allergic diseases</topic><topic>Apoptosis - physiology</topic><topic>apoptotic eosinophils</topic><topic>apoptotic neutrophils</topic><topic>Biological and medical sciences</topic><topic>Bronchi - immunology</topic><topic>Bronchi - physiology</topic><topic>Cells, Cultured</topic><topic>Eosinophils - physiology</topic><topic>epithelial cells</topic><topic>Epithelial Cells - immunology</topic><topic>Epithelial Cells - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Hyaluronan Receptors - immunology</topic><topic>Immunopathology</topic><topic>Integrins - physiology</topic><topic>Interleukin-1 - immunology</topic><topic>Jumonji Domain-Containing Histone Demethylases</topic><topic>Lectins - physiology</topic><topic>macrophage</topic><topic>Macrophages - physiology</topic><topic>Medical sciences</topic><topic>Microscopy, Confocal - methods</topic><topic>Microscopy, Electron - methods</topic><topic>Microscopy, Electron, Scanning - methods</topic><topic>Neutrophils - physiology</topic><topic>phagocytosis</topic><topic>Phagocytosis - physiology</topic><topic>Receptors, Cell Surface - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sexton, D. W.</creatorcontrib><creatorcontrib>Al-Rabia, M.</creatorcontrib><creatorcontrib>Blaylock, M. G.</creatorcontrib><creatorcontrib>Walsh, G. M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sexton, D. W.</au><au>Al-Rabia, M.</au><au>Blaylock, M. G.</au><au>Walsh, G. 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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