mortality/aging
• in response to LPS challenge in a model of acute septic shock
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immune system
• impaired cell death in response to CTB, E. coli, C. rodentium and V. cholerae
• however, bone marrow-derived macrophages stimulated with ATP of C. difficile toxin B exhibit normal cell death
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• in response to LPS challenge in a model of acute septic shock
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• in response to LPS challenge in a model of acute septic shock
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• in response to LPS challenge in a model of acute septic shock
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• from LPS-primed bone marrow-derived macrophage in response to CTB and E. coli
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• from LPS-primed bone marrow-derived macrophages in response to cholera toxin B (CTB), E. coli, C. rodentium or V. cholera (with or without LPS priming)
• however, secretion in response to poly(dA:dT) double-stranded DNA, Francisella tularensis, flagellin, Pseudomonas aeruginosa adenylcyclase (AC) toxin14, listeriolysin O (LLO) toxin15, Clostridium difficile toxin B, monosodium urate (MSU), calcium pyrophosphate (CPPD)2,22 or the ionophore nigericin is normal
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• mice are resistant to LPS challenge in a model of acute septic shock with reduced mortality and serum levels of IL1b, IL1a and IL18
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cellular
• impaired cell death in response to CTB, E. coli, C. rodentium and V. cholerae
• however, bone marrow-derived macrophages stimulated with ATP of C. difficile toxin B exhibit normal cell death
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homeostasis/metabolism
• in response to LPS challenge in a model of acute septic shock
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• in response to LPS challenge in a model of acute septic shock
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• in response to LPS challenge in a model of acute septic shock
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• in response to LPS challenge in a model of acute septic shock
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hematopoietic system
• impaired cell death in response to CTB, E. coli, C. rodentium and V. cholerae
• however, bone marrow-derived macrophages stimulated with ATP of C. difficile toxin B exhibit normal cell death
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