cellular
• 5 days after lung injury, mutants show significantly increased numbers of apoptotic lung epithelial and inflammatory cells
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homeostasis/metabolism
• mutant mice are more sensitive to hyperoxia; survival time of mutants after hyperoxia exposure is reduced by almost 50% compared to wild-type
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• double knockout mice are more susceptible to bleomycin-induced lung injury
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immune system
• hyaluronan fragment-induced expression of chemokines by peritoneal macrophages is completely abolished in double knockout mice
• 5 days after lung injury, mutant mice produce significantly lower amounts of chemotactic factor KC in the alveolar space
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respiratory system
• lung tissue from mutant mice shows evidence of enhanced injury with thickened interstitium and increased inflammatory cell accumulation within the interstitium
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