mortality/aging
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• following LPS-induced shock, mice exhibit less mortality (27% compared to 52%) and die later (3.5 days post-treatment compared to 1.5 days post-treatment) compared to wild-type mice
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immune system
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• chemotaxis in response to KC and macrophage-inflammatory protein-2 was reduced in homozygous mutant neutrophils compared to wild-type
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• 31% reduction in the number of neutrophils that are recruited to the lung following lipopolysaccharide (LPS) inhalation compared to wild-type and homozygous Pde4a mutants
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• LPS-stimulated TNF-alpha production is decreased to 43.5+/-3.5% of that in control mice
• thioglycollate-elicited macrophages produce 52.5+/-7.8% of TNF-alpha compared with wild-type cells
• macrophages do not respond to rolipram inhibition of LPS-stimulated TNF-alpha production
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cellular
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• chemotaxis in response to KC and macrophage-inflammatory protein-2 was reduced in homozygous mutant neutrophils compared to wild-type
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hematopoietic system
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• chemotaxis in response to KC and macrophage-inflammatory protein-2 was reduced in homozygous mutant neutrophils compared to wild-type
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• 31% reduction in the number of neutrophils that are recruited to the lung following lipopolysaccharide (LPS) inhalation compared to wild-type and homozygous Pde4a mutants
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