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Infect. Immun., 06 1996, 2010-2018, Vol 64, No. 6
E Grunvald, M Chiaramonte, S Hieny, M Wysocka, G Trinchieri, SN Vogel, RT Gazzinelli and A Sher
Previous reports have indicated that the early induction of interleukin- 12
(IL-12), tumor necrosis factor alpha (TNF-alpha), IL-1beta, and IL- 10 is
crucial for the establishment and regulation of host cell- mediated
immunity to the intracellular protozoan parasite Toxoplasma gondii. In this
study, we demonstrate that a soluble tachyzoite extract (soluble tachyzoite
antigen) can trigger the expression of these four monokines by murine
inflammatory macrophages. Further characterization revealed that the
parasite molecules in soluble tachyzoite antigen responsible for monokine
induction are heat stable at 100 degree C but differ in sensitivity to
protease digestion. Thus, the tachyzoite factors that stimulate TNF-alpha
and IL-to expression were found to be more resistant to treatment with
proteinase K than those responsible for IL-12 and IL-10 induction.
Similarly, while the factors responsible for the induction of all four
monokines were found to be sensitive to periodate oxidation, the
TNF-alpha-stimulating activity was partially resistant to treatment with
the compound at a low concentration (1 mM). A further dichotomy in monokine
induction signals was inferred from experiments with isoquinoline
sulfonamide protein kinase inhibitors. The latter work suggested that the
pathways for TNF-alpha and IL-1beta are protein kinase C dependent, while
expression of IL-12 and expression of IL-10 share distinct signal
transduction mechanisms involving other kinases. Together, these data argue
that monokine induction by T. gondii is mediated by glycoproteins that may
belong to distinct groups in terms of their biochemical properties and
intracellular signaling pathways.
Copyright © 1996, American Society for Microbiology
Biochemical characterization and protein kinase C dependency of monokine-inducing activities of Toxoplasma gondii
Immunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, USA.
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