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PMID: 8519093 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Activated microglia inhibit multiplication of Toxoplasma gondii via a nitric oxide mechanism.

Clinical immunology and immunopathology ·Vol. 67 ·No. 2 ·1993-05-00 ·Pages 178-83

Chao CC, Anderson WR, Hu S, Gekker G, Martella A, Peterson PK

Abstract

The role of microglia in host defense against Toxoplasma gondii is unknown. In the present study, we investigated the multiplication of T. gondii tachyzoites in murine microglial cell cultures. T. gondii multiplied readily in these cells; multiplication was prevented when microglia were activated with interferon-gamma plus lipopolysaccharide, a treatment that also upregulates nitric oxide (NO) synthase activity. Simultaneous treatment of microglial cell cultures with activation signals and the NO synthase inhibitor NG-monomethyl-L-arginine (NGMA) prevented the antitoxoplasmic activity. Transmission electron microscopic analysis demonstrated degenerative tachyzoites in activated microglia but not in control or NGMA groups. These findings support the view that the host defense function of activated microglia against T. gondii involves generation of the free radical NO.

MeSH Terms
Animals Cells, Cultured Interferon-gamma/pharmacology Lipopolysaccharides/pharmacology Macrophage Activation Macrophages/immunology,metabolism,parasitology,ultrastructure Mice Mice, Inbred BALB C Microscopy, Electron Neuroglia/immunology,metabolism,parasitology,ultrastructure Nitric Oxide/metabolism Toxoplasma/growth & development,immunology
Chemicals
Lipopolysaccharides Nitric Oxide Interferon-gamma
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Chao C C
Neuroimmunobiology and Host Defense Laboratory, Minneapolis Medical Research Foundation, Minnesota 55404.
Anderson W R
Hu S
Gekker G
Martella A
Peterson P K
Article Info
Journal
Clinical immunology and immunopathology
Abbr.
Clin Immunol Immunopathol
ISSN
0090-1229
Published
1993-05-00
Pages
178-83
Language
English
Region
United States
NLM ID
0356637
Subset
IM
Grants
NIDA NIH HHS · DA-04381 · United States
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