rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2007-11-22
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pubmed:abstractText |
In the present study, we tested the hypothesis that exposure of newborn mice to sublethal hyperoxia would alter lung development and expressions of fibroblast growth factor receptors (FGFRs)-3 and FGFR-4. Newborn FVB mice were exposed to 85% O2 or maintained in room air for up to 14 d. No animal mortality was observed, and body weight gains were not affected by hyperoxia. At postnatal d 7 and 14 (P7, P14), lungs of mice exposed to 85% O2 showed fewer alveolar secondary crests and larger alveoli or terminal air spaces than did mice in room air. In pups kept in room air, lung levels of FGFR-3 and FGFR-4 mRNA were greater at P3 than at P1, but similar increases were not observed in hyperoxic mice. Immunoreactivity of FGFR-3 and FGFR-4 was lower in lungs of hyperoxic mice than in controls at P14. In pups kept in room air, lung fibroblast growth factor (FGF)-7 mRNA levels were greater at P14 than at P1, but similar changes were not observed in hyperoxic mice. The temporally and spatially specific alterations in the expressions of FGFR-3, FGFR-4, and FGF-7 in the mice exposed to hyperoxia may contribute to aberrant lung development.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Fgf7 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Fgfr3 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Fgfr4 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 7,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth...
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0031-3998
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
652-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17957151-Age Factors,
pubmed-meshheading:17957151-Aging,
pubmed-meshheading:17957151-Animals,
pubmed-meshheading:17957151-Animals, Newborn,
pubmed-meshheading:17957151-Disease Models, Animal,
pubmed-meshheading:17957151-Fibroblast Growth Factor 7,
pubmed-meshheading:17957151-Gene Expression Regulation, Developmental,
pubmed-meshheading:17957151-Hyperoxia,
pubmed-meshheading:17957151-Lung,
pubmed-meshheading:17957151-Male,
pubmed-meshheading:17957151-Mice,
pubmed-meshheading:17957151-Oxygen,
pubmed-meshheading:17957151-Pulmonary Alveoli,
pubmed-meshheading:17957151-RNA, Messenger,
pubmed-meshheading:17957151-Receptor, Fibroblast Growth Factor, Type 3,
pubmed-meshheading:17957151-Receptor, Fibroblast Growth Factor, Type 4
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pubmed:year |
2007
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pubmed:articleTitle |
Altered expressions of fibroblast growth factor receptors and alveolarization in neonatal mice exposed to 85% oxygen.
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pubmed:affiliation |
Department of Pediatrics, Columbus Children's Research Institute, Columbus, Ohio 43205, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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