immune system
• improved cell viability following transfection with poly(dA:dT) or pcDNA3
• improved bone marrow derived macrophage viability following infection with F. tularensis
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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 or peritoneal macrophages stimulated by dsDNA
• bone marrow derived macrophages do not secrete IL1B in response to F. tularensis
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• in LPS-primed bone marrow derived macrophages stimulated by dsDNA
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• in bone marrow derived macrophages stimulated by poly(dA:dT) or pcDNA3
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• fail to control F. tularensis infection
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hematopoietic system
• improved cell viability following transfection with poly(dA:dT) or pcDNA3
• improved bone marrow derived macrophage viability following infection with F. tularensis
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