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Epidermal growth factor receptor signaling mediates regranulation of rat nasal goblet cells

Background: Mucus hypersecretion is a common response to inflammation in the lower airways and is a hallmark of chronic rhinitis. Objective: The purpose of this study was to elucidate the mechanisms of regranulation (mucus production) of goblet cells in nasal epithelium. Methods: Because neutrophils...

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Published in:Journal of allergy and clinical immunology 2001-06, Vol.107 (6), p.1046-1050
Main Authors: Lee, Heung-Man, Malm, Lars, Dabbagh, Karim, Dao-Pick, Trang, Ueki, Iris F., Kim, Suil, Shim, Jae Jeong, Nadel, Jay A.
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cited_by cdi_FETCH-LOGICAL-c444t-900a86d1b0502efc260c624493e0df0fe7788926ecccd2418da04c4937ec57c13
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container_issue 6
container_start_page 1046
container_title Journal of allergy and clinical immunology
container_volume 107
creator Lee, Heung-Man
Malm, Lars
Dabbagh, Karim
Dao-Pick, Trang
Ueki, Iris F.
Kim, Suil
Shim, Jae Jeong
Nadel, Jay A.
description Background: Mucus hypersecretion is a common response to inflammation in the lower airways and is a hallmark of chronic rhinitis. Objective: The purpose of this study was to elucidate the mechanisms of regranulation (mucus production) of goblet cells in nasal epithelium. Methods: Because neutrophils induce an epidermal growth factor (EGFR) cascade, we induced degranulation of goblet cells in rat nasal respiratory epithelium by means of intranasal inhalation of N-formyl-methionyl-leucyl-phenylalanine (fMLP), and we examined regranulation of the goblet cells and the role of EGFR inhibitors and neutrophils in the regranulation process. Results: In the control state Alcian blue/periodic acid–Schiff and mucin MUC5AC staining was present. Degranulation was induced in the nasal septal epithelium 4 hours after intranasal inhalation of fMLP (10–7 mol/L); 48 hours later, goblet-cell regranulation was complete. In the control state EGFR protein staining was absent in the epithelium, but after fMLP-induced degranulation, EGFR protein was expressed. After pretreatment with BIBX1522, a selective EGFR tyrosine kinase inhibitor, fMLP-induced degranulation was unaffected, but goblet-cell regranulation was prevented completely. Conclusion: These data suggest a role for the EGFR cascade in neutrophil-dependent production of goblet-cell mucins. Proving this theory will require the use of selective EGFR inhibitors in clinical studies of nasal hypersecretory states. (J Allergy Clin Immunol 2001;107:1046-50.)
doi_str_mv 10.1067/mai.2001.115140
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Objective: The purpose of this study was to elucidate the mechanisms of regranulation (mucus production) of goblet cells in nasal epithelium. Methods: Because neutrophils induce an epidermal growth factor (EGFR) cascade, we induced degranulation of goblet cells in rat nasal respiratory epithelium by means of intranasal inhalation of N-formyl-methionyl-leucyl-phenylalanine (fMLP), and we examined regranulation of the goblet cells and the role of EGFR inhibitors and neutrophils in the regranulation process. Results: In the control state Alcian blue/periodic acid–Schiff and mucin MUC5AC staining was present. Degranulation was induced in the nasal septal epithelium 4 hours after intranasal inhalation of fMLP (10–7 mol/L); 48 hours later, goblet-cell regranulation was complete. In the control state EGFR protein staining was absent in the epithelium, but after fMLP-induced degranulation, EGFR protein was expressed. After pretreatment with BIBX1522, a selective EGFR tyrosine kinase inhibitor, fMLP-induced degranulation was unaffected, but goblet-cell regranulation was prevented completely. Conclusion: These data suggest a role for the EGFR cascade in neutrophil-dependent production of goblet-cell mucins. Proving this theory will require the use of selective EGFR inhibitors in clinical studies of nasal hypersecretory states. 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Stomatology ; Phosphorylation ; Protein-Tyrosine Kinases - antagonists &amp; inhibitors ; Protein-Tyrosine Kinases - metabolism ; Rats ; Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors ; Receptor, Epidermal Growth Factor - metabolism ; Secretory cell growth ; Signal Transduction ; Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><ispartof>Journal of allergy and clinical immunology, 2001-06, Vol.107 (6), p.1046-1050</ispartof><rights>2001 Mosby, Inc.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-900a86d1b0502efc260c624493e0df0fe7788926ecccd2418da04c4937ec57c13</citedby><cites>FETCH-LOGICAL-c444t-900a86d1b0502efc260c624493e0df0fe7788926ecccd2418da04c4937ec57c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1062770$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11398083$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Heung-Man</creatorcontrib><creatorcontrib>Malm, Lars</creatorcontrib><creatorcontrib>Dabbagh, Karim</creatorcontrib><creatorcontrib>Dao-Pick, Trang</creatorcontrib><creatorcontrib>Ueki, Iris F.</creatorcontrib><creatorcontrib>Kim, Suil</creatorcontrib><creatorcontrib>Shim, Jae Jeong</creatorcontrib><creatorcontrib>Nadel, Jay A.</creatorcontrib><title>Epidermal growth factor receptor signaling mediates regranulation of rat nasal goblet cells</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Background: Mucus hypersecretion is a common response to inflammation in the lower airways and is a hallmark of chronic rhinitis. Objective: The purpose of this study was to elucidate the mechanisms of regranulation (mucus production) of goblet cells in nasal epithelium. Methods: Because neutrophils induce an epidermal growth factor (EGFR) cascade, we induced degranulation of goblet cells in rat nasal respiratory epithelium by means of intranasal inhalation of N-formyl-methionyl-leucyl-phenylalanine (fMLP), and we examined regranulation of the goblet cells and the role of EGFR inhibitors and neutrophils in the regranulation process. Results: In the control state Alcian blue/periodic acid–Schiff and mucin MUC5AC staining was present. Degranulation was induced in the nasal septal epithelium 4 hours after intranasal inhalation of fMLP (10–7 mol/L); 48 hours later, goblet-cell regranulation was complete. In the control state EGFR protein staining was absent in the epithelium, but after fMLP-induced degranulation, EGFR protein was expressed. After pretreatment with BIBX1522, a selective EGFR tyrosine kinase inhibitor, fMLP-induced degranulation was unaffected, but goblet-cell regranulation was prevented completely. Conclusion: These data suggest a role for the EGFR cascade in neutrophil-dependent production of goblet-cell mucins. Proving this theory will require the use of selective EGFR inhibitors in clinical studies of nasal hypersecretory states. 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Stomatology</subject><subject>Phosphorylation</subject><subject>Protein-Tyrosine Kinases - antagonists &amp; inhibitors</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Rats</subject><subject>Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Secretory cell growth</subject><subject>Signal Transduction</subject><subject>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkT1P5DAQhi0EguWjpkMp0HVZxok3tkuEuOOklWi4isLyTiaLURIvthfEvz9Hu9LRoKs81jzzavQMY5cc5hwaeTNYN68A-JzzBRdwwGYctCwbVS0O2QxA87KRQp-w0xhfIf9rpY_ZCee1VqDqGXu-37iWwmD7Yh38R3opOovJhyIQ0mYqoluPtnfjuhiodTZRzL11sOO2t8n5sfBdEWwqRhunEL_qKRVIfR_P2VFn-0gX-_eM_fl5_3T3UC4ff_2-u12WKIRIpQawqmn5ChZQUYdVA9hUQuiaoO2gIymV0lVDiNhWgqvWgsDcloQLibw-Yz92uZvg37YUkxlcnDawI_ltNDJrUEqI_4JccQW1msCbHYjBxxioM5vgBhs-DQcziTdZvJnEm534PHG1j96usqd__N50Bq73gI1o-y4LRBe_5DaVlFOO3mGUhb07CiaioxGz-nyRZFrvvt3hLwl-ntI</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Lee, Heung-Man</creator><creator>Malm, Lars</creator><creator>Dabbagh, Karim</creator><creator>Dao-Pick, Trang</creator><creator>Ueki, Iris F.</creator><creator>Kim, Suil</creator><creator>Shim, Jae Jeong</creator><creator>Nadel, Jay A.</creator><general>Mosby, Inc</general><general>Elsevier</general><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>7X8</scope></search><sort><creationdate>20010601</creationdate><title>Epidermal growth factor receptor signaling mediates regranulation of rat nasal goblet cells</title><author>Lee, Heung-Man ; Malm, Lars ; Dabbagh, Karim ; Dao-Pick, Trang ; Ueki, Iris F. ; Kim, Suil ; Shim, Jae Jeong ; Nadel, Jay A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-900a86d1b0502efc260c624493e0df0fe7788926ecccd2418da04c4937ec57c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Administration, Intranasal</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>epidermal growth factor receptor cascade</topic><topic>epidermal growth factor receptor tyrosine kinase activation</topic><topic>epidermal growth factor receptors</topic><topic>Goblet Cells - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mucin 5AC</topic><topic>mucin expression</topic><topic>Mucins - metabolism</topic><topic>Mucus - secretion</topic><topic>N-formyl-Met-Leu-Phe</topic><topic>N-Formylmethionine Leucyl-Phenylalanine - administration &amp; dosage</topic><topic>nasal hypersecretion</topic><topic>Nasal Mucosa - cytology</topic><topic>Nasal Mucosa - immunology</topic><topic>Neutrophil Activation - immunology</topic><topic>Neutrophils - immunology</topic><topic>Non tumoral diseases</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Phosphorylation</topic><topic>Protein-Tyrosine Kinases - antagonists &amp; inhibitors</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Rats</topic><topic>Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Secretory cell growth</topic><topic>Signal Transduction</topic><topic>Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Heung-Man</creatorcontrib><creatorcontrib>Malm, Lars</creatorcontrib><creatorcontrib>Dabbagh, Karim</creatorcontrib><creatorcontrib>Dao-Pick, Trang</creatorcontrib><creatorcontrib>Ueki, Iris F.</creatorcontrib><creatorcontrib>Kim, Suil</creatorcontrib><creatorcontrib>Shim, Jae Jeong</creatorcontrib><creatorcontrib>Nadel, Jay A.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Heung-Man</au><au>Malm, Lars</au><au>Dabbagh, Karim</au><au>Dao-Pick, Trang</au><au>Ueki, Iris F.</au><au>Kim, Suil</au><au>Shim, Jae Jeong</au><au>Nadel, Jay A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidermal growth factor receptor signaling mediates regranulation of rat nasal goblet cells</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>107</volume><issue>6</issue><spage>1046</spage><epage>1050</epage><pages>1046-1050</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Background: Mucus hypersecretion is a common response to inflammation in the lower airways and is a hallmark of chronic rhinitis. Objective: The purpose of this study was to elucidate the mechanisms of regranulation (mucus production) of goblet cells in nasal epithelium. Methods: Because neutrophils induce an epidermal growth factor (EGFR) cascade, we induced degranulation of goblet cells in rat nasal respiratory epithelium by means of intranasal inhalation of N-formyl-methionyl-leucyl-phenylalanine (fMLP), and we examined regranulation of the goblet cells and the role of EGFR inhibitors and neutrophils in the regranulation process. Results: In the control state Alcian blue/periodic acid–Schiff and mucin MUC5AC staining was present. Degranulation was induced in the nasal septal epithelium 4 hours after intranasal inhalation of fMLP (10–7 mol/L); 48 hours later, goblet-cell regranulation was complete. In the control state EGFR protein staining was absent in the epithelium, but after fMLP-induced degranulation, EGFR protein was expressed. After pretreatment with BIBX1522, a selective EGFR tyrosine kinase inhibitor, fMLP-induced degranulation was unaffected, but goblet-cell regranulation was prevented completely. Conclusion: These data suggest a role for the EGFR cascade in neutrophil-dependent production of goblet-cell mucins. Proving this theory will require the use of selective EGFR inhibitors in clinical studies of nasal hypersecretory states. (J Allergy Clin Immunol 2001;107:1046-50.)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>11398083</pmid><doi>10.1067/mai.2001.115140</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of allergy and clinical immunology, 2001-06, Vol.107 (6), p.1046-1050
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subjects Administration, Intranasal
Animals
Biological and medical sciences
Enzyme Inhibitors - pharmacology
epidermal growth factor receptor cascade
epidermal growth factor receptor tyrosine kinase activation
epidermal growth factor receptors
Goblet Cells - physiology
Male
Medical sciences
Mucin 5AC
mucin expression
Mucins - metabolism
Mucus - secretion
N-formyl-Met-Leu-Phe
N-Formylmethionine Leucyl-Phenylalanine - administration & dosage
nasal hypersecretion
Nasal Mucosa - cytology
Nasal Mucosa - immunology
Neutrophil Activation - immunology
Neutrophils - immunology
Non tumoral diseases
Otorhinolaryngology. Stomatology
Phosphorylation
Protein-Tyrosine Kinases - antagonists & inhibitors
Protein-Tyrosine Kinases - metabolism
Rats
Receptor, Epidermal Growth Factor - antagonists & inhibitors
Receptor, Epidermal Growth Factor - metabolism
Secretory cell growth
Signal Transduction
Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
title Epidermal growth factor receptor signaling mediates regranulation of rat nasal goblet cells
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