Infection and Immunity · 1996 · 117 citations · 35 references
Life SciencesImmunologyMicrobiologyHost-pathogen InteractionsInflammationInnate ImmunityBacterial ImmunologyCellular Immune ResponsesCytokine BiologyImmune Responses To InfectionInflammation In Infectious DiseaseMacrophage BiologyBacterial Lipopolysaccharide RecognitionBone Marrow - Derived CellsCell ActivationEndotoxin-mediated InflammationMacrophage ImmunomodulationMacrophage Responses To BacteriaMurine ModelsReceptors
We studied the ability of the lipopolysaccharide (LPS) extracted from a vaccine strain of Francisella tularensis (LPS-Ft) to mimic LPSs from other gram-negative bacteria for activation of various murine cell types or to antagonize the effects of other LPSs. We found that activation of macrophages for the production of tumor necrosis factor alpha and NO, of pre-B lymphocytes for the expression of surface immunoglobulins, and of bone marrow cells for the expression of LPS-binding sites was either undetectable with LPS-Ft or required concentrations 100 to 1,000 times higher than for standard LPSs. Preexposure of macrophages to LPS-Ft also failed to trigger down-regulation of tumor necrosis factor alpha (desensitization) or up-regulation of NO responses to an endotoxin challenge. In contrast to other atypical LPSs, LPS-Ft was also unable to antagonize any of the endotoxin-induced cellular responses mentioned above, suggesting that this LPS does not interact with LPS receptors.
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Aihao Ding, Carl Nathan, Dennis J. Stuehr · The Journal of Immunology · 1988 · 2.8K citations · Full text
Chemical Coupling of Proteins to Agarose
Jerker Porath, Rolf Axén, Sverker Ernback · Nature · 1967 · 978 citations