mortality/aging
• after intestinal ischemia/reperfusion (IIR) injury in 7- to 10-week old animals, mortality at 24 hours is 15% compared to 25% in wild-type controls
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respiratory system
N |
• 7-10 week-old mutants show normal lung morphology; blood gas analyses and bronchoalveolar lavage for total and differential cell counts are not different from controls
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• acute lung injury (ALI) is ameliorated in 7- to 10-week-old mutants after IIR
• fibrin deposition is rare along alveolar septa and absent within alveolar spaces after IIR in contrast to wild-type at 7 to 10 weeks where dense deposits of fibrin are detected in small vessels and along alveolar septa
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• interstitial edema is lower in mutants after IIR compared to controls at 7 to 10 weeks
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• during acute lung injury effected by IIR in 7- to 10-week old animals, epithelial cell death via caspase-dependent mechanisms is significantly higher in mutants than in wild-type controls
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• pulmonary vascular permeability is significantly lower than in wild-type controls at 7 to 10 weeks of age
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• following IIR in 7- to 10-week old animals, inflammatory mononuclear cell infiltration is significantly reduced compare to wild-type controls
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• emphysema is detected in animals at 28- to 32-weeks of age; significant airspace enlargement is seen histologically and increased lung volume is observed in some cases compared to wild-type mice
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homeostasis/metabolism
• interstitial edema is lower in mutants after IIR compared to controls at 7 to 10 weeks
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cardiovascular system
• pulmonary vascular permeability is significantly lower than in wild-type controls at 7 to 10 weeks of age
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immune system
• following IIR in 7- to 10-week old animals, inflammatory mononuclear cell infiltration is significantly reduced compare to wild-type controls
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