immune system
• improved bone marrow derived macrophage viability following infection with F. tularensis
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• in response to LPS challenge in a model of acute septic shock
|
• in response to LPS challenge in a model of acute septic shock
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• in bone marrow derived macrophages stimulated by poly(dA:dT) or pcDNA3
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• in LPS-primed bone marrow derived macrophages stimulated by S. typhimurium or dsDNA
(J:160545)
• bone marrow derived macrophages do not secrete IL1B in response to F. tularensis
(J:160545)
• from LPS-primed bone marrow-derived macrophages stimulated with E. coli, C. rodentium, C. cholera and CTB
(J:193522)
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• in bone marrow derived macrophages stimulated by poly(dA:dT) or pcDNA3
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• mice treated with LPS challenge in a model of acute septic shock exhibit reduced serum levels of IL1b and IL18 compared with controls
• however, mice do not survive beyond 20 hours and serum levels of IL1a are increased
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homeostasis/metabolism
• in response to LPS challenge in a model of acute septic shock
|
• in response to LPS challenge in a model of acute septic shock
|
hematopoietic system
• improved bone marrow derived macrophage viability following infection with F. tularensis
|