Comparative gene expression profiling of post-natal and post-pneumonectomy lung growth
Although increasing numbers of patients suffer from chronic destructive lung diseases, there are no effective therapeutic options apart from transplantation. Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapie...
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Veröffentlicht in: | The European respiratory journal 2010-03, Vol.35 (3), p.655-666 |
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description | Although increasing numbers of patients suffer from chronic destructive lung diseases, there are no effective therapeutic options apart from transplantation. Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapies for the lung. We compared lung gene expression in the phase of induction of post-natal and post-pneumonectomy alveolarisation to identify regulatory genes involved in both processes. We performed genome-wide microarray screenings of newborn and pneumonectomised mouse lungs 1 and 3 days after birth or surgery. Selected candidates were validated by real-time PCR, Western blot and in situ hybridisation. We found 58 genes to be regulated in both models with 40 candidates being changed likewise. Many of these genes participated in growth and differentiation processes. Additionally, immune system, structural molecules, respiratory chain, signal transduction and metabolism were involved. Some candidates were not yet linked to specific functions. The highest regulatory concordance was observed for various isoforms of (pro-)collagen molecules, elastin and the elastin-associated protein fibrillin1 being corporately upregulated. Our findings do not definitively support a common regulating mechanism for induction of post-natal and adult alveolarisation, but some candidates in the intersection of both models are promising for further investigations. |
doi_str_mv | 10.1183/09031936.00059709 |
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Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapies for the lung. We compared lung gene expression in the phase of induction of post-natal and post-pneumonectomy alveolarisation to identify regulatory genes involved in both processes. We performed genome-wide microarray screenings of newborn and pneumonectomised mouse lungs 1 and 3 days after birth or surgery. Selected candidates were validated by real-time PCR, Western blot and in situ hybridisation. We found 58 genes to be regulated in both models with 40 candidates being changed likewise. Many of these genes participated in growth and differentiation processes. Additionally, immune system, structural molecules, respiratory chain, signal transduction and metabolism were involved. Some candidates were not yet linked to specific functions. The highest regulatory concordance was observed for various isoforms of (pro-)collagen molecules, elastin and the elastin-associated protein fibrillin1 being corporately upregulated. 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Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapies for the lung. We compared lung gene expression in the phase of induction of post-natal and post-pneumonectomy alveolarisation to identify regulatory genes involved in both processes. We performed genome-wide microarray screenings of newborn and pneumonectomised mouse lungs 1 and 3 days after birth or surgery. Selected candidates were validated by real-time PCR, Western blot and in situ hybridisation. We found 58 genes to be regulated in both models with 40 candidates being changed likewise. Many of these genes participated in growth and differentiation processes. Additionally, immune system, structural molecules, respiratory chain, signal transduction and metabolism were involved. Some candidates were not yet linked to specific functions. The highest regulatory concordance was observed for various isoforms of (pro-)collagen molecules, elastin and the elastin-associated protein fibrillin1 being corporately upregulated. Our findings do not definitively support a common regulating mechanism for induction of post-natal and adult alveolarisation, but some candidates in the intersection of both models are promising for further investigations.</description><subject>Acute-Phase Proteins - genetics</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Elastin - genetics</subject><subject>Elastin - metabolism</subject><subject>Fibrillin-1</subject><subject>Fibrillins</subject><subject>Gene Expression Profiling</subject><subject>Genes, fos</subject><subject>Humans</subject><subject>In Situ Hybridization</subject><subject>Lipocalin-2</subject><subject>Lipocalins - genetics</subject><subject>Liver Regeneration - genetics</subject><subject>Lung - growth & development</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microfilament Proteins - genetics</subject><subject>Microfilament Proteins - metabolism</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Oncogene Proteins - genetics</subject><subject>Pneumology</subject><subject>Pneumonectomy</subject><subject>Polymerase Chain Reaction</subject><subject>Procollagen - genetics</subject><subject>Procollagen - metabolism</subject><subject>Up-Regulation</subject><issn>0903-1936</issn><issn>1399-3003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1v1DAQhi0EotvCD-CCckGcUmbsOF4f0ap8SJW4AFfLcSa7rhw72Aml_56sdtueRqN53lejh7F3CNeIW_EJNAjUor0GAKkV6Bdsg0LrWgCIl2xzvNdH4IJdlnIHgG0j8DW7QK1QNdtmw37v0jjZbGf_l6o9Raro35SpFJ9iNeU0-ODjvkpDNaUy19HONlQ29qd1irSMKZKb0_hQhWUl9zndz4c37NVgQ6G353nFfn25-bn7Vt_--Pp99_m2dg2IuUbuXN8Baaf7BpHIdS2C6p10W6W5053i3JKSw_o75x1uJfVW912rpBs6EFfs46l3ffXPQmU2oy-OQrCR0lKMEqIBlEKsJJ5Il1MpmQYzZT_a_GAQzNGmebRpHm2umffn9qUbqX9OnPWtwIczYIuzYcg2Ol-eOM4b0Lzhz9zB7w_3PpMpow1hrUVD-U5II0wrpfgPbC6Kvw</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Wolff, J-C</creator><creator>Wilhelm, J</creator><creator>Fink, L</creator><creator>Seeger, W</creator><creator>Voswinckel, R</creator><general>Eur Respiratory Soc</general><general>Maney</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>7X8</scope></search><sort><creationdate>20100301</creationdate><title>Comparative gene expression profiling of post-natal and post-pneumonectomy lung growth</title><author>Wolff, J-C ; Wilhelm, J ; Fink, L ; Seeger, W ; Voswinckel, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-12ccdb0e9c9d411eecb6107dc5c8792c9b722ae75f00122b185eda9db675cfb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acute-Phase Proteins - genetics</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Elastin - genetics</topic><topic>Elastin - metabolism</topic><topic>Fibrillin-1</topic><topic>Fibrillins</topic><topic>Gene Expression Profiling</topic><topic>Genes, fos</topic><topic>Humans</topic><topic>In Situ Hybridization</topic><topic>Lipocalin-2</topic><topic>Lipocalins - genetics</topic><topic>Liver Regeneration - genetics</topic><topic>Lung - growth & development</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microfilament Proteins - genetics</topic><topic>Microfilament Proteins - metabolism</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Oncogene Proteins - genetics</topic><topic>Pneumology</topic><topic>Pneumonectomy</topic><topic>Polymerase Chain Reaction</topic><topic>Procollagen - genetics</topic><topic>Procollagen - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wolff, J-C</creatorcontrib><creatorcontrib>Wilhelm, J</creatorcontrib><creatorcontrib>Fink, L</creatorcontrib><creatorcontrib>Seeger, W</creatorcontrib><creatorcontrib>Voswinckel, R</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>MEDLINE - Academic</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wolff, J-C</au><au>Wilhelm, J</au><au>Fink, L</au><au>Seeger, W</au><au>Voswinckel, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative gene expression profiling of post-natal and post-pneumonectomy lung growth</atitle><jtitle>The European respiratory journal</jtitle><addtitle>Eur Respir J</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>35</volume><issue>3</issue><spage>655</spage><epage>666</epage><pages>655-666</pages><issn>0903-1936</issn><eissn>1399-3003</eissn><abstract>Although increasing numbers of patients suffer from chronic destructive lung diseases, there are no effective therapeutic options apart from transplantation. Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapies for the lung. We compared lung gene expression in the phase of induction of post-natal and post-pneumonectomy alveolarisation to identify regulatory genes involved in both processes. We performed genome-wide microarray screenings of newborn and pneumonectomised mouse lungs 1 and 3 days after birth or surgery. Selected candidates were validated by real-time PCR, Western blot and in situ hybridisation. We found 58 genes to be regulated in both models with 40 candidates being changed likewise. Many of these genes participated in growth and differentiation processes. Additionally, immune system, structural molecules, respiratory chain, signal transduction and metabolism were involved. Some candidates were not yet linked to specific functions. The highest regulatory concordance was observed for various isoforms of (pro-)collagen molecules, elastin and the elastin-associated protein fibrillin1 being corporately upregulated. Our findings do not definitively support a common regulating mechanism for induction of post-natal and adult alveolarisation, but some candidates in the intersection of both models are promising for further investigations.</abstract><cop>Leeds</cop><pub>Eur Respiratory Soc</pub><pmid>19717484</pmid><doi>10.1183/09031936.00059709</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute-Phase Proteins - genetics Animals Animals, Newborn Biological and medical sciences Blotting, Western Elastin - genetics Elastin - metabolism Fibrillin-1 Fibrillins Gene Expression Profiling Genes, fos Humans In Situ Hybridization Lipocalin-2 Lipocalins - genetics Liver Regeneration - genetics Lung - growth & development Male Medical sciences Mice Microfilament Proteins - genetics Microfilament Proteins - metabolism Oligonucleotide Array Sequence Analysis Oncogene Proteins - genetics Pneumology Pneumonectomy Polymerase Chain Reaction Procollagen - genetics Procollagen - metabolism Up-Regulation |
title | Comparative gene expression profiling of post-natal and post-pneumonectomy lung growth |
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