Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model
Combined results from laser capture microdissection of mouse airway epithelial cells followed by high power (MALDI-FTICR) MS, and fluorescent two-dimensional gel elctrophoresis (2D-DIGE) of the whole lung, allowed us to identify proteins differentially expressed after naphthalene induced airway inju...
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Veröffentlicht in: | Journal of proteome research 2009-07, Vol.8 (7), p.3606-3616 |
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creator | Carvalho-Oliveira, Isabel M Charro, Nuno Aarbiou, Jamil Buijs-Offerman, Ruvalic M Wilke, Martina Schettgen, Thomas Kraus, Thomas Titulaer, Mark K Burgers, Peter Luider, Theo M Penque, Deborah Scholte, Bob J |
description | Combined results from laser capture microdissection of mouse airway epithelial cells followed by high power (MALDI-FTICR) MS, and fluorescent two-dimensional gel elctrophoresis (2D-DIGE) of the whole lung, allowed us to identify proteins differentially expressed after naphthalene induced airway injury. Further, we discovered several novel aspects of Cystic Fibrosis (CF) lung pathology in an F508del-Cftr mouse model using this approach. The combined MALDI-FTICR−MS and 2D-DIGE data show that lung carbonyl reductase (CBR2), involved in prostaglandin metabolism, converting PGE2 to PGF2alpha, is localized to airway cells and is reduced 2-fold in mutant mice compared to normal, both before and after challenge. Further, we observe a downregulation of two key enzymes of retinoic acid metabolism after injury, which is more pronounced in CF mutant mice. These data show that state-of-the-art proteomics can be used to evaluate airway injury in small cell samples. Further, the results suggest the involvement of prostaglandin and retinoic acid metabolism in the abnormal responses of CF mutant mice to injury. |
doi_str_mv | 10.1021/pr900021m |
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Further, we discovered several novel aspects of Cystic Fibrosis (CF) lung pathology in an F508del-Cftr mouse model using this approach. The combined MALDI-FTICR−MS and 2D-DIGE data show that lung carbonyl reductase (CBR2), involved in prostaglandin metabolism, converting PGE2 to PGF2alpha, is localized to airway cells and is reduced 2-fold in mutant mice compared to normal, both before and after challenge. Further, we observe a downregulation of two key enzymes of retinoic acid metabolism after injury, which is more pronounced in CF mutant mice. These data show that state-of-the-art proteomics can be used to evaluate airway injury in small cell samples. Further, the results suggest the involvement of prostaglandin and retinoic acid metabolism in the abnormal responses of CF mutant mice to injury.</description><identifier>ISSN: 1535-3893</identifier><identifier>EISSN: 1535-3907</identifier><identifier>DOI: 10.1021/pr900021m</identifier><identifier>PMID: 19438287</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Cystic Fibrosis - genetics ; Cystic Fibrosis - metabolism ; Electrophoresis, Gel, Two-Dimensional ; Epithelium - pathology ; Lung - pathology ; Male ; Mice ; Mice, Inbred CFTR - metabolism ; Mice, Transgenic ; Naphthalenes - pharmacology ; Proteome ; Proteomics - methods ; Respiratory Mucosa - pathology ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Tretinoin - metabolism</subject><ispartof>Journal of proteome research, 2009-07, Vol.8 (7), p.3606-3616</ispartof><rights>Copyright © 2009 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a379t-3623ec7826523678d542dd7e85fb2708025ba20b28bbc1985fc1768a2b7f6d653</citedby><cites>FETCH-LOGICAL-a379t-3623ec7826523678d542dd7e85fb2708025ba20b28bbc1985fc1768a2b7f6d653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/pr900021m$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/pr900021m$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19438287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carvalho-Oliveira, Isabel M</creatorcontrib><creatorcontrib>Charro, Nuno</creatorcontrib><creatorcontrib>Aarbiou, Jamil</creatorcontrib><creatorcontrib>Buijs-Offerman, Ruvalic M</creatorcontrib><creatorcontrib>Wilke, Martina</creatorcontrib><creatorcontrib>Schettgen, Thomas</creatorcontrib><creatorcontrib>Kraus, Thomas</creatorcontrib><creatorcontrib>Titulaer, Mark K</creatorcontrib><creatorcontrib>Burgers, Peter</creatorcontrib><creatorcontrib>Luider, Theo M</creatorcontrib><creatorcontrib>Penque, Deborah</creatorcontrib><creatorcontrib>Scholte, Bob J</creatorcontrib><title>Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model</title><title>Journal of proteome research</title><addtitle>J. Proteome Res</addtitle><description>Combined results from laser capture microdissection of mouse airway epithelial cells followed by high power (MALDI-FTICR) MS, and fluorescent two-dimensional gel elctrophoresis (2D-DIGE) of the whole lung, allowed us to identify proteins differentially expressed after naphthalene induced airway injury. Further, we discovered several novel aspects of Cystic Fibrosis (CF) lung pathology in an F508del-Cftr mouse model using this approach. The combined MALDI-FTICR−MS and 2D-DIGE data show that lung carbonyl reductase (CBR2), involved in prostaglandin metabolism, converting PGE2 to PGF2alpha, is localized to airway cells and is reduced 2-fold in mutant mice compared to normal, both before and after challenge. Further, we observe a downregulation of two key enzymes of retinoic acid metabolism after injury, which is more pronounced in CF mutant mice. These data show that state-of-the-art proteomics can be used to evaluate airway injury in small cell samples. Further, the results suggest the involvement of prostaglandin and retinoic acid metabolism in the abnormal responses of CF mutant mice to injury.</description><subject>Animals</subject><subject>Cystic Fibrosis - genetics</subject><subject>Cystic Fibrosis - metabolism</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Epithelium - pathology</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred CFTR - metabolism</subject><subject>Mice, Transgenic</subject><subject>Naphthalenes - pharmacology</subject><subject>Proteome</subject><subject>Proteomics - methods</subject><subject>Respiratory Mucosa - pathology</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Tretinoin - metabolism</subject><issn>1535-3893</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkMtKAzEUhoMotlYXvoBko-BiNJdmklmW0mqhXhBdD5kkQ1MyF5MZZN7elFbduDnn5_DxcfgBuMToDiOC71ufIRRDdQTGmFGW0Azx458sMjoCZyFsEcKMI3oKRjibUkEEH4P61TedaSqr4KyWbgg2wKaEz7LddBvpTG2SVa17ZTScWf8lB7hobbcxzkoHV_W29wOUtYZvppXWQ1tDCedD6KJvaQvf7HxPTR9MnNq4c3BSShfMxWFPwMdy8T5_TNYvD6v5bJ1IyrMuoSmhRnFBUkZoyoVmU6I1N4KVBeFIIMIKSVBBRFEonMWzwjwVkhS8THXK6ATc7L2tbz57E7q8skEZ52Rt4jd5yqeMs3Qawds9qOKvwZsyb72tpB9yjPJduflvuZG9Okj7ojL6jzy0GYHrPSBVyLdN72Oj4R_RN8UngHU</recordid><startdate>20090706</startdate><enddate>20090706</enddate><creator>Carvalho-Oliveira, Isabel M</creator><creator>Charro, Nuno</creator><creator>Aarbiou, Jamil</creator><creator>Buijs-Offerman, Ruvalic M</creator><creator>Wilke, Martina</creator><creator>Schettgen, Thomas</creator><creator>Kraus, Thomas</creator><creator>Titulaer, Mark K</creator><creator>Burgers, Peter</creator><creator>Luider, Theo M</creator><creator>Penque, Deborah</creator><creator>Scholte, Bob J</creator><general>American Chemical Society</general><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>7X8</scope></search><sort><creationdate>20090706</creationdate><title>Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model</title><author>Carvalho-Oliveira, Isabel M ; Charro, Nuno ; Aarbiou, Jamil ; Buijs-Offerman, Ruvalic M ; Wilke, Martina ; Schettgen, Thomas ; Kraus, Thomas ; Titulaer, Mark K ; Burgers, Peter ; Luider, Theo M ; Penque, Deborah ; Scholte, Bob J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a379t-3623ec7826523678d542dd7e85fb2708025ba20b28bbc1985fc1768a2b7f6d653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cystic Fibrosis - genetics</topic><topic>Cystic Fibrosis - metabolism</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Epithelium - pathology</topic><topic>Lung - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred CFTR - metabolism</topic><topic>Mice, Transgenic</topic><topic>Naphthalenes - pharmacology</topic><topic>Proteome</topic><topic>Proteomics - methods</topic><topic>Respiratory Mucosa - pathology</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Tretinoin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carvalho-Oliveira, Isabel M</creatorcontrib><creatorcontrib>Charro, Nuno</creatorcontrib><creatorcontrib>Aarbiou, Jamil</creatorcontrib><creatorcontrib>Buijs-Offerman, Ruvalic M</creatorcontrib><creatorcontrib>Wilke, Martina</creatorcontrib><creatorcontrib>Schettgen, Thomas</creatorcontrib><creatorcontrib>Kraus, Thomas</creatorcontrib><creatorcontrib>Titulaer, Mark K</creatorcontrib><creatorcontrib>Burgers, Peter</creatorcontrib><creatorcontrib>Luider, Theo M</creatorcontrib><creatorcontrib>Penque, Deborah</creatorcontrib><creatorcontrib>Scholte, Bob J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carvalho-Oliveira, Isabel M</au><au>Charro, Nuno</au><au>Aarbiou, Jamil</au><au>Buijs-Offerman, Ruvalic M</au><au>Wilke, Martina</au><au>Schettgen, Thomas</au><au>Kraus, Thomas</au><au>Titulaer, Mark K</au><au>Burgers, Peter</au><au>Luider, Theo M</au><au>Penque, Deborah</au><au>Scholte, Bob J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2009-07-06</date><risdate>2009</risdate><volume>8</volume><issue>7</issue><spage>3606</spage><epage>3616</epage><pages>3606-3616</pages><issn>1535-3893</issn><eissn>1535-3907</eissn><abstract>Combined results from laser capture microdissection of mouse airway epithelial cells followed by high power (MALDI-FTICR) MS, and fluorescent two-dimensional gel elctrophoresis (2D-DIGE) of the whole lung, allowed us to identify proteins differentially expressed after naphthalene induced airway injury. Further, we discovered several novel aspects of Cystic Fibrosis (CF) lung pathology in an F508del-Cftr mouse model using this approach. The combined MALDI-FTICR−MS and 2D-DIGE data show that lung carbonyl reductase (CBR2), involved in prostaglandin metabolism, converting PGE2 to PGF2alpha, is localized to airway cells and is reduced 2-fold in mutant mice compared to normal, both before and after challenge. 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subjects | Animals Cystic Fibrosis - genetics Cystic Fibrosis - metabolism Electrophoresis, Gel, Two-Dimensional Epithelium - pathology Lung - pathology Male Mice Mice, Inbred CFTR - metabolism Mice, Transgenic Naphthalenes - pharmacology Proteome Proteomics - methods Respiratory Mucosa - pathology Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Tretinoin - metabolism |
title | Proteomic Analysis of Naphthalene-Induced Airway Epithelial Injury and Repair in a Cystic Fibrosis Mouse Model |
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