DISCORDANT PULMONARY PROINFLAMMATORY CYTOKINE EXPRESSION DURING ACUTE HYPEROXIA IN THE NEWBORN RABBIT
Newborn animals are resistant to oxygen toxicity. To investigate this phenomenon, the proinflammatory cytokines interleukin (IL)-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) were measured during newborn rabbit hyperoxic lung injury. Pups were exposed to 95 > % O2 for 8-9 days, foll...
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Veröffentlicht in: | Experimental lung research 1999, Vol.25 (5), p.443-465 |
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description | Newborn animals are resistant to oxygen toxicity. To investigate this phenomenon, the proinflammatory cytokines interleukin (IL)-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) were measured during newborn rabbit hyperoxic lung injury. Pups were exposed to 95 > % O2 for 8-9 days, followed by 60% O2 until 36 days of age. Lung lavage fluid, RNA, and tissue sections were collected at 0, 2, 4, 6, 8, 10, 12, 14, 22, and 36 days. Acute inflammation occurred by 6 - 10 days of hyperoxia, and fibrosis by 22 days. Northern hybridization of lung homogenates from hyperoxia - exposed pups showed elevated MCP-1 and IL-8 mRNA expression at 6 and 10 days, respectively, compared to age - matched, air - exposed controls. Lavage fluid IL-8 protein also peaked at 10 days, and was strongly correlated to neutrophil numbers in lavage. In situ hybridization revealed elevated IL-1beta mRNA in macrophages, alveolar epithelial and interstitial cells at 2-10days, elevated MCP-1 mRNA in similar cell types at 4-8 days, and elevated IL-8 mRNA in these cells and neutrophils at 4-10 days. IL-1beta and IL-8 expression peaked during peak inflammation, whereas peak MCP-1 expression preceded macrophage influx. Comparing newborn and adult animals' chemokine responses may help explain their differences in hyperoxia susceptibility. |
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T ; LOMONACO, M. B ; CHAUDHRY, S. A ; PAXHIA, A ; RYAN, R. M</creator><creatorcontrib>D'ANGIO, C. T ; LOMONACO, M. B ; CHAUDHRY, S. A ; PAXHIA, A ; RYAN, R. M</creatorcontrib><description>Newborn animals are resistant to oxygen toxicity. To investigate this phenomenon, the proinflammatory cytokines interleukin (IL)-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) were measured during newborn rabbit hyperoxic lung injury. Pups were exposed to 95 > % O2 for 8-9 days, followed by 60% O2 until 36 days of age. Lung lavage fluid, RNA, and tissue sections were collected at 0, 2, 4, 6, 8, 10, 12, 14, 22, and 36 days. Acute inflammation occurred by 6 - 10 days of hyperoxia, and fibrosis by 22 days. Northern hybridization of lung homogenates from hyperoxia - exposed pups showed elevated MCP-1 and IL-8 mRNA expression at 6 and 10 days, respectively, compared to age - matched, air - exposed controls. Lavage fluid IL-8 protein also peaked at 10 days, and was strongly correlated to neutrophil numbers in lavage. In situ hybridization revealed elevated IL-1beta mRNA in macrophages, alveolar epithelial and interstitial cells at 2-10days, elevated MCP-1 mRNA in similar cell types at 4-8 days, and elevated IL-8 mRNA in these cells and neutrophils at 4-10 days. IL-1beta and IL-8 expression peaked during peak inflammation, whereas peak MCP-1 expression preceded macrophage influx. Comparing newborn and adult animals' chemokine responses may help explain their differences in hyperoxia susceptibility.</description><identifier>ISSN: 0190-2148</identifier><identifier>EISSN: 1521-0499</identifier><identifier>DOI: 10.1080/019021499270187</identifier><identifier>PMID: 10483526</identifier><identifier>CODEN: EXLRDA</identifier><language>eng</language><publisher>Philadelphia, PA: Informa UK Ltd</publisher><subject>Animals ; Animals, Newborn - metabolism ; Biological and medical sciences ; Blotting, Northern ; Bronchoalveolar Lavage Fluid - chemistry ; Cell Count ; Chemokine CCL2 - genetics ; Chemokine CCL2 - metabolism ; Chemokines;Interleukin-1beta;Interleukin-8;Lung;Monocyte Chemoattractant Protein-1;Oxygen Toxicity;Pulmonary Inflammation ; Disease Models, Animal ; Enzyme-Linked Immunosorbent Assay ; Epithelial Cells - metabolism ; Fundamental and applied biological sciences. Psychology ; Hyperoxia - metabolism ; In Situ Hybridization ; Inflammation ; Interleukin-1 - genetics ; Interleukin-1 - metabolism ; Interleukin-8 - genetics ; Interleukin-8 - metabolism ; Lung - metabolism ; Lung - pathology ; Macrophages, Alveolar - cytology ; Macrophages, Alveolar - metabolism ; Molecular and cellular biology ; Oxygen - blood ; Pulmonary Alveoli - cytology ; Pulmonary Alveoli - metabolism ; Pulmonary Fibrosis - metabolism ; Pulmonary Fibrosis - pathology ; Rabbits ; RNA, Messenger - analysis ; RNA, Messenger - metabolism</subject><ispartof>Experimental lung research, 1999, Vol.25 (5), p.443-465</ispartof><rights>1999 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1999</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-69dccfcaf9a5445579c7aec8e19c5377b20533a9fdfdae22e898f2bf234a706b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/019021499270187$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/019021499270187$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,777,781,4010,27904,27905,27906,59626,60415,61200,61381</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1912874$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10483526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>D'ANGIO, C. T</creatorcontrib><creatorcontrib>LOMONACO, M. B</creatorcontrib><creatorcontrib>CHAUDHRY, S. A</creatorcontrib><creatorcontrib>PAXHIA, A</creatorcontrib><creatorcontrib>RYAN, R. M</creatorcontrib><title>DISCORDANT PULMONARY PROINFLAMMATORY CYTOKINE EXPRESSION DURING ACUTE HYPEROXIA IN THE NEWBORN RABBIT</title><title>Experimental lung research</title><addtitle>Exp Lung Res</addtitle><description>Newborn animals are resistant to oxygen toxicity. To investigate this phenomenon, the proinflammatory cytokines interleukin (IL)-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) were measured during newborn rabbit hyperoxic lung injury. Pups were exposed to 95 > % O2 for 8-9 days, followed by 60% O2 until 36 days of age. Lung lavage fluid, RNA, and tissue sections were collected at 0, 2, 4, 6, 8, 10, 12, 14, 22, and 36 days. Acute inflammation occurred by 6 - 10 days of hyperoxia, and fibrosis by 22 days. Northern hybridization of lung homogenates from hyperoxia - exposed pups showed elevated MCP-1 and IL-8 mRNA expression at 6 and 10 days, respectively, compared to age - matched, air - exposed controls. Lavage fluid IL-8 protein also peaked at 10 days, and was strongly correlated to neutrophil numbers in lavage. In situ hybridization revealed elevated IL-1beta mRNA in macrophages, alveolar epithelial and interstitial cells at 2-10days, elevated MCP-1 mRNA in similar cell types at 4-8 days, and elevated IL-8 mRNA in these cells and neutrophils at 4-10 days. IL-1beta and IL-8 expression peaked during peak inflammation, whereas peak MCP-1 expression preceded macrophage influx. Comparing newborn and adult animals' chemokine responses may help explain their differences in hyperoxia susceptibility.</description><subject>Animals</subject><subject>Animals, Newborn - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Bronchoalveolar Lavage Fluid - chemistry</subject><subject>Cell Count</subject><subject>Chemokine CCL2 - genetics</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Chemokines;Interleukin-1beta;Interleukin-8;Lung;Monocyte Chemoattractant Protein-1;Oxygen Toxicity;Pulmonary Inflammation</subject><subject>Disease Models, Animal</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epithelial Cells - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hyperoxia - metabolism</subject><subject>In Situ Hybridization</subject><subject>Inflammation</subject><subject>Interleukin-1 - genetics</subject><subject>Interleukin-1 - metabolism</subject><subject>Interleukin-8 - genetics</subject><subject>Interleukin-8 - metabolism</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Macrophages, Alveolar - cytology</subject><subject>Macrophages, Alveolar - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Oxygen - blood</subject><subject>Pulmonary Alveoli - cytology</subject><subject>Pulmonary Alveoli - metabolism</subject><subject>Pulmonary Fibrosis - metabolism</subject><subject>Pulmonary Fibrosis - pathology</subject><subject>Rabbits</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><issn>0190-2148</issn><issn>1521-0499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtPwzAQhC0EgvI4c0M-cA21naSxuaVpaC1au0pTQU-R69iiKG0qpwjx7wkqiIfEabU736x2B4BLjG4woqiLMEMEB4yRCGEaHYAODgn2UDs5BJ0P1WtlegJOm-YZIURC2jsGJxgF1A9JrwPMgM8SmQ1ikcPpfDyRIs4WcJpJLu7G8WQS57Ltk0Uu77lIYfo4zdLZjEsBB_OMiyGMk3mewtFimmbykceQC5iPUijSh77MBMzifp_n5-DIqqoxF5_1DMzv0jwZeWM55Ek89nRA_J3XY6XWVivLVBgEYRgxHSmjqcFMh34ULQkKfV8xW9pSGUIMZdSSpSV-oCLUW_pnoLvfq13dNM7YYutWa-XeCoyKj8CKP4G1jqu9Y_uyXJvyB79PqAWuPwHVaFVZpzZ61XxzDBMaBS12u8dWG1u7tXqtXVUWO_VW1e7L4_9_BPtlfjKq2j1p5UzxXL-4TRvZvw-8A9I0jyk</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>D'ANGIO, C. T</creator><creator>LOMONACO, M. B</creator><creator>CHAUDHRY, S. A</creator><creator>PAXHIA, A</creator><creator>RYAN, R. M</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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></search><sort><creationdate>1999</creationdate><title>DISCORDANT PULMONARY PROINFLAMMATORY CYTOKINE EXPRESSION DURING ACUTE HYPEROXIA IN THE NEWBORN RABBIT</title><author>D'ANGIO, C. T ; LOMONACO, M. B ; CHAUDHRY, S. A ; PAXHIA, A ; RYAN, R. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-69dccfcaf9a5445579c7aec8e19c5377b20533a9fdfdae22e898f2bf234a706b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Animals, Newborn - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Bronchoalveolar Lavage Fluid - chemistry</topic><topic>Cell Count</topic><topic>Chemokine CCL2 - genetics</topic><topic>Chemokine CCL2 - metabolism</topic><topic>Chemokines;Interleukin-1beta;Interleukin-8;Lung;Monocyte Chemoattractant Protein-1;Oxygen Toxicity;Pulmonary Inflammation</topic><topic>Disease Models, Animal</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epithelial Cells - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hyperoxia - metabolism</topic><topic>In Situ Hybridization</topic><topic>Inflammation</topic><topic>Interleukin-1 - genetics</topic><topic>Interleukin-1 - metabolism</topic><topic>Interleukin-8 - genetics</topic><topic>Interleukin-8 - metabolism</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Macrophages, Alveolar - cytology</topic><topic>Macrophages, Alveolar - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Oxygen - blood</topic><topic>Pulmonary Alveoli - cytology</topic><topic>Pulmonary Alveoli - metabolism</topic><topic>Pulmonary Fibrosis - metabolism</topic><topic>Pulmonary Fibrosis - pathology</topic><topic>Rabbits</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>D'ANGIO, C. T</creatorcontrib><creatorcontrib>LOMONACO, M. B</creatorcontrib><creatorcontrib>CHAUDHRY, S. A</creatorcontrib><creatorcontrib>PAXHIA, A</creatorcontrib><creatorcontrib>RYAN, R. M</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><jtitle>Experimental lung research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>D'ANGIO, C. T</au><au>LOMONACO, M. B</au><au>CHAUDHRY, S. A</au><au>PAXHIA, A</au><au>RYAN, R. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DISCORDANT PULMONARY PROINFLAMMATORY CYTOKINE EXPRESSION DURING ACUTE HYPEROXIA IN THE NEWBORN RABBIT</atitle><jtitle>Experimental lung research</jtitle><addtitle>Exp Lung Res</addtitle><date>1999</date><risdate>1999</risdate><volume>25</volume><issue>5</issue><spage>443</spage><epage>465</epage><pages>443-465</pages><issn>0190-2148</issn><eissn>1521-0499</eissn><coden>EXLRDA</coden><abstract>Newborn animals are resistant to oxygen toxicity. To investigate this phenomenon, the proinflammatory cytokines interleukin (IL)-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) were measured during newborn rabbit hyperoxic lung injury. Pups were exposed to 95 > % O2 for 8-9 days, followed by 60% O2 until 36 days of age. Lung lavage fluid, RNA, and tissue sections were collected at 0, 2, 4, 6, 8, 10, 12, 14, 22, and 36 days. Acute inflammation occurred by 6 - 10 days of hyperoxia, and fibrosis by 22 days. Northern hybridization of lung homogenates from hyperoxia - exposed pups showed elevated MCP-1 and IL-8 mRNA expression at 6 and 10 days, respectively, compared to age - matched, air - exposed controls. Lavage fluid IL-8 protein also peaked at 10 days, and was strongly correlated to neutrophil numbers in lavage. In situ hybridization revealed elevated IL-1beta mRNA in macrophages, alveolar epithelial and interstitial cells at 2-10days, elevated MCP-1 mRNA in similar cell types at 4-8 days, and elevated IL-8 mRNA in these cells and neutrophils at 4-10 days. IL-1beta and IL-8 expression peaked during peak inflammation, whereas peak MCP-1 expression preceded macrophage influx. Comparing newborn and adult animals' chemokine responses may help explain their differences in hyperoxia susceptibility.</abstract><cop>Philadelphia, PA</cop><pub>Informa UK Ltd</pub><pmid>10483526</pmid><doi>10.1080/019021499270187</doi><tpages>23</tpages></addata></record> |
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subjects | Animals Animals, Newborn - metabolism Biological and medical sciences Blotting, Northern Bronchoalveolar Lavage Fluid - chemistry Cell Count Chemokine CCL2 - genetics Chemokine CCL2 - metabolism Chemokines Interleukin-1beta Interleukin-8 Lung Monocyte Chemoattractant Protein-1 Oxygen Toxicity Pulmonary Inflammation Disease Models, Animal Enzyme-Linked Immunosorbent Assay Epithelial Cells - metabolism Fundamental and applied biological sciences. Psychology Hyperoxia - metabolism In Situ Hybridization Inflammation Interleukin-1 - genetics Interleukin-1 - metabolism Interleukin-8 - genetics Interleukin-8 - metabolism Lung - metabolism Lung - pathology Macrophages, Alveolar - cytology Macrophages, Alveolar - metabolism Molecular and cellular biology Oxygen - blood Pulmonary Alveoli - cytology Pulmonary Alveoli - metabolism Pulmonary Fibrosis - metabolism Pulmonary Fibrosis - pathology Rabbits RNA, Messenger - analysis RNA, Messenger - metabolism |
title | DISCORDANT PULMONARY PROINFLAMMATORY CYTOKINE EXPRESSION DURING ACUTE HYPEROXIA IN THE NEWBORN RABBIT |
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