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Infect. Immun., 05 1997, 1734-1741, Vol 65, No. 5
Y Shibata, LA Foster, WJ Metzger and QN Myrvik
Intravenous (i.v.) administration of phagocytosable chitin particles (1 to
10 microm) in C57BL/6 mice and SCID mice primed alveolar macrophages (Mphi)
within 3 days to yield up to a 50-fold increase in their oxidative burst
when elicited in vitro with phorbol myristate acetate (PMA). C57BL/6 mice
pretreated with monoclonal antibodies (MAbs) against mouse gamma interferon
(IFN-gamma) or NK1.1 showed a markedly decreased level of alveolar Mphi
priming following injection of chitin particles. To confirm IFN-gamma
production in vitro, spleen cells isolated from normal C57BL/6 mice and
SCID mice were cultured with chitin particles. Significant IFN-gamma
production was observed following stimulation with chitin but not with
chitosan or latex beads. When spleen cells were treated with anti-NK1.1
MAb, IFN-gamma production was significantly inhibited. Another set of
experiments showed that when C57BL/6 mice were pretreated i.v. with a small
dose IFN-gamma, a higher level of priming was induced with not only
phagocytosable chitin particles but also phagocytosable chitosan and even
latex beads. Likewise, the spleen cell cultures preconditioned with
IFN-gamma provided an up-regulation of IFN-gamma production by these
phagocytosable particles. Taken together, the in vivo and in vitro results
suggest that (i) the alveolar Mphi priming mechanism is due, at least in
part, to direct activation of Mphi by IFN-gamma, which is produced by
NK1.1+ CD4- cells; (ii) IFN-gamma would have an autocrine-like effect on
Mphi and make them more responsive to particle priming; and (iii)
phagocytosis of particulates, probably by a postmembrane event such as
interiorization, appears to be important for the up-regulation of alveolar
Mphi priming and IFN-gamma production.
Copyright © 1997, American Society for Microbiology
Alveolar macrophage priming by intravenous administration of chitin particles, polymers of N-acetyl-D-glucosamine, in mice
Department of Medicine, East Carolina University School of Medicine, Greenville, North Carolina 27858, USA.
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