Insulin decreases expression of the proinflammatory receptor proteinase-activated receptor-2 on human airway epithelial cells
Insulin resistance is associated with allergic sensitization and allergic asthma in human subjects2,3 and animal models.4 Recent evidence shows decreased insulin receptor expression in the airway epithelium of asthmatic patients,5 suggesting the presence of insulin resistance in the asthmatic epithe...
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Veröffentlicht in: | Journal of allergy and clinical immunology 2018-09, Vol.142 (3), p.1003-1006.e8 |
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description | Insulin resistance is associated with allergic sensitization and allergic asthma in human subjects2,3 and animal models.4 Recent evidence shows decreased insulin receptor expression in the airway epithelium of asthmatic patients,5 suggesting the presence of insulin resistance in the asthmatic epithelium. [...]airway inflammation in asthmatic patients could be, at least in part, the result of decrease in insulin-mediated anti-inflammatory mechanisms in the airways. Proteinase-activated receptor-2 (PAR-2) is a G protein–coupled receptor involved in the pathogenesis of a number of inflammatory conditions,E1-E6 including allergic asthma,6,7 a condition with increased PAR-2 expression on airway epithelial cells (AECs).8 Based on a previous observation that PAR-2 expression and PAR-2–mediated inflammation increase in insulin-resistant adipose tissue,E7-E9 we hypothesized that insulin regulates PAR-2 expression also in the airways. Detailed methods are described in the Methods section in this article's Online Repository at www.jacionline.org. Because high-fat diet (HFD)–induced insulin resistance modulates PAR-2 expression in adipose tissue,E7-E9 we studied PAR-2 expression in the lungs of HFD-fed mice. [...]the FOXO-1 inhibitor AS1842856 prevented insulin deficiency–induced PAR-2 upregulation in submerged (Fig 2, G) and ALI cultures of AECs (Fig 2, H). |
doi_str_mv | 10.1016/j.jaci.2018.04.040 |
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[...]airway inflammation in asthmatic patients could be, at least in part, the result of decrease in insulin-mediated anti-inflammatory mechanisms in the airways. Proteinase-activated receptor-2 (PAR-2) is a G protein–coupled receptor involved in the pathogenesis of a number of inflammatory conditions,E1-E6 including allergic asthma,6,7 a condition with increased PAR-2 expression on airway epithelial cells (AECs).8 Based on a previous observation that PAR-2 expression and PAR-2–mediated inflammation increase in insulin-resistant adipose tissue,E7-E9 we hypothesized that insulin regulates PAR-2 expression also in the airways. Detailed methods are described in the Methods section in this article's Online Repository at www.jacionline.org. Because high-fat diet (HFD)–induced insulin resistance modulates PAR-2 expression in adipose tissue,E7-E9 we studied PAR-2 expression in the lungs of HFD-fed mice. [...]the FOXO-1 inhibitor AS1842856 prevented insulin deficiency–induced PAR-2 upregulation in submerged (Fig 2, G) and ALI cultures of AECs (Fig 2, H).</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2018.04.040</identifier><identifier>PMID: 29890235</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Asthma ; Binding sites ; Epithelial cells ; Hypotheses ; Inflammation ; Insulin ; Insulin resistance ; Lungs ; Obesity ; Pathogenesis ; Proteinase ; Proteins ; Respiratory tract</subject><ispartof>Journal of allergy and clinical immunology, 2018-09, Vol.142 (3), p.1003-1006.e8</ispartof><rights>2018 American Academy of Allergy, Asthma & Immunology</rights><rights>Copyright Elsevier Limited Sep 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-fa60abda6a32ef4d8a7c1034cfd06d7f343ba76789baa31c4c031a4ad8eae0e33</citedby><cites>FETCH-LOGICAL-c428t-fa60abda6a32ef4d8a7c1034cfd06d7f343ba76789baa31c4c031a4ad8eae0e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaci.2018.04.040$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29890235$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gandhi, Vivek D.</creatorcontrib><creatorcontrib>Shrestha Palikhe, Nami</creatorcontrib><creatorcontrib>Hamza, Shereen M.</creatorcontrib><creatorcontrib>Dyck, Jason R.B.</creatorcontrib><creatorcontrib>Buteau, Jean</creatorcontrib><creatorcontrib>Vliagoftis, Harissios</creatorcontrib><title>Insulin decreases expression of the proinflammatory receptor proteinase-activated receptor-2 on human airway epithelial cells</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Insulin resistance is associated with allergic sensitization and allergic asthma in human subjects2,3 and animal models.4 Recent evidence shows decreased insulin receptor expression in the airway epithelium of asthmatic patients,5 suggesting the presence of insulin resistance in the asthmatic epithelium. [...]airway inflammation in asthmatic patients could be, at least in part, the result of decrease in insulin-mediated anti-inflammatory mechanisms in the airways. Proteinase-activated receptor-2 (PAR-2) is a G protein–coupled receptor involved in the pathogenesis of a number of inflammatory conditions,E1-E6 including allergic asthma,6,7 a condition with increased PAR-2 expression on airway epithelial cells (AECs).8 Based on a previous observation that PAR-2 expression and PAR-2–mediated inflammation increase in insulin-resistant adipose tissue,E7-E9 we hypothesized that insulin regulates PAR-2 expression also in the airways. Detailed methods are described in the Methods section in this article's Online Repository at www.jacionline.org. Because high-fat diet (HFD)–induced insulin resistance modulates PAR-2 expression in adipose tissue,E7-E9 we studied PAR-2 expression in the lungs of HFD-fed mice. [...]the FOXO-1 inhibitor AS1842856 prevented insulin deficiency–induced PAR-2 upregulation in submerged (Fig 2, G) and ALI cultures of AECs (Fig 2, H).</description><subject>Asthma</subject><subject>Binding sites</subject><subject>Epithelial cells</subject><subject>Hypotheses</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Lungs</subject><subject>Obesity</subject><subject>Pathogenesis</subject><subject>Proteinase</subject><subject>Proteins</subject><subject>Respiratory tract</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kUuLFTEQhYMoznX0D7iQgBs3fa08bncCbmTwMTDgRtehblLNpOmXSfc4d-F_N80dZ-FCKEhCfXVyqMPYawF7AaJ-3-079HEvQZg96FLwhO0E2KaqjTw8ZTsAK6q60faCvci5g_JWxj5nF9IaC1Idduz39ZjXPo48kE-EmTKn-zlRznEa-dTy5Zb4nKY4tj0OAy5TOvFEnuZy2xoLxbGMVeiXeIcLhcduJXmRuF0HHDnG9AtPnOZY9PqIPffU9_kle9Zin-nVw3nJfnz-9P3qa3Xz7cv11cebymtplqrFGvAYsEYlqdXBYOMFKO3bAHVoWqXVEZu6MfaIqITXHpRAjcEQEpBSl-zdWbcY_rlSXtwQ8-YAR5rW7CQctFXlr7qgb_9Bu2lNY3FXKGuVNVKZQskz5dOUc6LWzSkOmE5OgNvCcZ3bwnFbOA50KShDbx6k1-NA4XHkbxoF-HAGqOziLlJy2UcaPYVYlrq4MMX_6f8Byfajog</recordid><startdate>201809</startdate><enddate>201809</enddate><creator>Gandhi, Vivek D.</creator><creator>Shrestha Palikhe, Nami</creator><creator>Hamza, Shereen M.</creator><creator>Dyck, Jason R.B.</creator><creator>Buteau, Jean</creator><creator>Vliagoftis, Harissios</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201809</creationdate><title>Insulin decreases expression of the proinflammatory receptor proteinase-activated receptor-2 on human airway epithelial cells</title><author>Gandhi, Vivek D. ; Shrestha Palikhe, Nami ; Hamza, Shereen M. ; Dyck, Jason R.B. ; Buteau, Jean ; Vliagoftis, Harissios</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-fa60abda6a32ef4d8a7c1034cfd06d7f343ba76789baa31c4c031a4ad8eae0e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Asthma</topic><topic>Binding sites</topic><topic>Epithelial cells</topic><topic>Hypotheses</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Lungs</topic><topic>Obesity</topic><topic>Pathogenesis</topic><topic>Proteinase</topic><topic>Proteins</topic><topic>Respiratory tract</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gandhi, Vivek D.</creatorcontrib><creatorcontrib>Shrestha Palikhe, Nami</creatorcontrib><creatorcontrib>Hamza, Shereen M.</creatorcontrib><creatorcontrib>Dyck, Jason R.B.</creatorcontrib><creatorcontrib>Buteau, Jean</creatorcontrib><creatorcontrib>Vliagoftis, Harissios</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</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>Gandhi, Vivek D.</au><au>Shrestha Palikhe, Nami</au><au>Hamza, Shereen M.</au><au>Dyck, Jason R.B.</au><au>Buteau, Jean</au><au>Vliagoftis, Harissios</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin decreases expression of the proinflammatory receptor proteinase-activated receptor-2 on human airway epithelial cells</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2018-09</date><risdate>2018</risdate><volume>142</volume><issue>3</issue><spage>1003</spage><epage>1006.e8</epage><pages>1003-1006.e8</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><abstract>Insulin resistance is associated with allergic sensitization and allergic asthma in human subjects2,3 and animal models.4 Recent evidence shows decreased insulin receptor expression in the airway epithelium of asthmatic patients,5 suggesting the presence of insulin resistance in the asthmatic epithelium. [...]airway inflammation in asthmatic patients could be, at least in part, the result of decrease in insulin-mediated anti-inflammatory mechanisms in the airways. Proteinase-activated receptor-2 (PAR-2) is a G protein–coupled receptor involved in the pathogenesis of a number of inflammatory conditions,E1-E6 including allergic asthma,6,7 a condition with increased PAR-2 expression on airway epithelial cells (AECs).8 Based on a previous observation that PAR-2 expression and PAR-2–mediated inflammation increase in insulin-resistant adipose tissue,E7-E9 we hypothesized that insulin regulates PAR-2 expression also in the airways. Detailed methods are described in the Methods section in this article's Online Repository at www.jacionline.org. Because high-fat diet (HFD)–induced insulin resistance modulates PAR-2 expression in adipose tissue,E7-E9 we studied PAR-2 expression in the lungs of HFD-fed mice. [...]the FOXO-1 inhibitor AS1842856 prevented insulin deficiency–induced PAR-2 upregulation in submerged (Fig 2, G) and ALI cultures of AECs (Fig 2, H).</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29890235</pmid><doi>10.1016/j.jaci.2018.04.040</doi><oa>free_for_read</oa></addata></record> |
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subjects | Asthma Binding sites Epithelial cells Hypotheses Inflammation Insulin Insulin resistance Lungs Obesity Pathogenesis Proteinase Proteins Respiratory tract |
title | Insulin decreases expression of the proinflammatory receptor proteinase-activated receptor-2 on human airway epithelial cells |
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