Infection and Immunity · 1986 · 39 citations · 19 references
Life SciencesImmunologyPhysiologyAgingDevelopmental ImmunologyInnate ImmunityBiological AgingImmune DevelopmentImmune OntogenyMacrophage BiologyReactive Oxygen SpeciesRodent PhysiologyAge-dependent ResponseMacrophage Function AlterationMacrophage ImmunobiologyMacrophage Inflammatory ResponsesMacrophage Oxidative StressMacrophage Reactive Oxygen Species ResponsesMacrophage Responses To Bacteria
To determine whether the presence of bacterial flora contributes to the ontogenic development of macrophage function, the ability of macrophages to release superoxide anion (O2-) in response to stimulation with phorbol myristate acetate was compared in conventional and germfree mice of various ages after birth. One-week-old conventional mice showed a very low level of O2- release by their macrophages, and gradual increases were observed in 2-, 3-, and 4-week-old mice in an age-dependent manner. Macrophages from germfree mice always showed a significantly lower level of O2- release compared with conventional mice of the same age; however, age-dependent functional development was seen also in the germfree group. The poor level of O2- release by macrophages from adult germfree mice could be restored to more than the level by conventional mice when the mice were conventionalized for 3 weeks. These results suggested that the ontogenic development of macrophage function is not controlled by the presence of bacterial flora but that the full-scale expression of function at each age is under the influence of microflora.
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