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
Hauptverfasser: D'ANGIO, C. T, LOMONACO, M. B, CHAUDHRY, S. A, PAXHIA, A, RYAN, R. M
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container_issue 5
container_start_page 443
container_title Experimental lung research
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creator D'ANGIO, C. T
LOMONACO, M. B
CHAUDHRY, S. A
PAXHIA, A
RYAN, R. M
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.
doi_str_mv 10.1080/019021499270187
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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 &gt; % 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. 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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. 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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. 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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 &gt; % 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. 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source MEDLINE; Taylor & Francis:Master (3349 titles)
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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