PLoS ONE · 2012 · 76 citations · 44 references
Life SciencesImmunologyInfectious DiseasesCell SignalingHost-pathogen InteractionsInnate ImmunityCellular Immune ResponsesImmunopathology Of Parasitic DiseaseInfectious Disease PathophysiologyInnate Immunity To ParasitesMacrophage BiologyParasitic Disease PathogenesisNitric OxideNitric Oxide BiologyNitric Oxide ProductionNitric Oxide SignalingNitric Oxide Synthase RegulationPathogenesis Of Parasitic ZoonosesPeritoneal MacrophagesToxoplasmosis Pathogenesis
Toxoplasma gondii infects humans and warm blooded animals causing devastating disease worldwide. It has long been a mystery as to why the peritoneal macrophages of rats are naturally resistant to T. gondii infection while those of mice are not. Here, we report that high expression levels and activity of inducible nitric oxide synthase (iNOS) and low levels of arginase-1 (Arg 1) activity in the peritoneal macrophages of rats are responsible for their resistance against T. gondii infection, due to high nitric oxide and low polyamines within these cells. The opposite situation was observed in the peritoneal macrophages of mice. This discovery of the opposing functions of iNOS and Arg 1 in rodent peritoneal macrophages may lead to a better understanding of the resistance mechanisms of mammals, particularly humans and livestock, against T. gondii and other intracellular pathogens.
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Aihao Ding, Carl Nathan, Dennis J. Stuehr · The Journal of Immunology · 1988 · 2.8K citations · Full text
W. L. Homan, Martine Vercammen, Jos De Braekeleer et al. · International Journal for Parasitology · 2000 · 739 citations
Matthias Hesse, Manuel Modolell, Anne Camille La Flamme et al. · The Journal of Immunology · 2001 · 681 citations · Full text