Bioscience Biotechnology and Biochemistry · 1999 · 21 citations · 20 references
Life SciencesEndocrinologyImmunologyImmunophysiologyInflammationInnate ImmunityCytokine BiologyCytokine-mediated PathologyInflammatory Cell ResponsesInnate Immune ActivationAcute-phase MediatorsAcute-phase ProteinsImmune Stress ResponseInflammatory Response To StressResponsivenessSerum Amyloid A ProteinStress Hormone Effects On Immunity
To determine why germfree mice are less susceptible to lipopolysaccharide (LPS) than conventional mice, we studied serum levels of serum amyloid A (SAA), tumor necrosis factor (TNF), interleukin 1 (IL-1), IL-6, and corticosterone in mice after treatment with LPS. A single injection of LPS caused an elevation of SAA, an acute-phase protein in the mouse, in both conventional and germfree IQI mice, and the response was significantly less in germfree mice. LPS-induced elevations of serum TNF, IL-1, and IL-6 levels were also significantly less in germfree mice, while serum corticosterone levels were greater in germfree mice than in conventional mice. These results suggest that the lower susceptibility to LPS and a smaller response of SAA elevation by LPS in germfree mice may result from less elevation in serum of these cytokines in these mice, which are known to mediate the acute phase response of SAA. High levels of serum corticosterone in germfree mice may be partly responsible for the lower responsiveness of these inflammatory cytokines to LPS in these mice.
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Soluble CD14 participates in the response of cells to lipopolysaccharide.
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