Source:http://linkedlifedata.com/resource/pubmed/id/11909735
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0040557,
umls-concept:C0185117,
umls-concept:C0332291,
umls-concept:C0542341,
umls-concept:C0597357,
umls-concept:C0812246,
umls-concept:C1419030,
umls-concept:C1420280,
umls-concept:C1456820,
umls-concept:C1515655,
umls-concept:C1533698,
umls-concept:C1706871,
umls-concept:C1707597,
umls-concept:C2911684
|
pubmed:issue |
3
|
pubmed:dateCreated |
2002-3-22
|
pubmed:abstractText |
Wild type, TNFRp55(-/-), iNOS(-/-) and IFN-gamma(-/-) mice were infected with Toxoplasma gondii strain ME-49, and the central nervous system (CNS), lungs, liver, spleen, heart and kidneys were examined for the presence of parasites expressing tachyzoite-specific (SAG-1) and bradyzoite-specific (BAG-5) antigens. During the acute phase of infection, the peripheral organs, but not the CNS, of the IFN-gamma(-/-) mice are heavily parasitized by tachyzoites and there are no signs of parasites expressing BAG-5. In contrast, the tissues from TNFRp55(-/-) and inducible nitric oxide synthase (iNOS)(-/-) mice, mainly the CNS, presented high numbers of parasites expressing SAG-1 and/or BAG-5. Tachyzoite transformation into bradyzoite and cyst development was shown to be normal in the tissues from TNFRp55(-/-) and iNOS(-/-) mice, as indicated by the high numbers of BAG-5/PAS positive cysts. Consistently, reactivation of infection in IFN-gamma(-/-) mice was rapid and characterized by a dramatic increase in SAG-1, contrasting with slow course in the TNFRp55(-/-) or iNOS(-/-) mice associated with a relatively small increase in SAG-1- and/or BAG-5-positive parasites. In conclusion, our results suggest that the control of multiplication of tachyzoites is largely dependent on endogenous IFN-gamma with partial involvement of TNFRp55 and iNOS. In contrast, induction of BAG-5 expression and cyst formation during toxoplasmosis seems to be dependent on IFN-gamma, but independent of TNFRp55 and iNOS functions.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Protozoan,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II,
http://linkedlifedata.com/resource/pubmed/chemical/Nos2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Protozoan Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor...,
http://linkedlifedata.com/resource/pubmed/chemical/SAG1 antigen, Toxoplasma
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1286-4579
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
4
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
261-70
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11909735-Animals,
pubmed-meshheading:11909735-Antigens, CD,
pubmed-meshheading:11909735-Antigens, Protozoan,
pubmed-meshheading:11909735-Cysts,
pubmed-meshheading:11909735-Female,
pubmed-meshheading:11909735-Host-Parasite Interactions,
pubmed-meshheading:11909735-Mice,
pubmed-meshheading:11909735-Mice, Inbred Strains,
pubmed-meshheading:11909735-Mice, Knockout,
pubmed-meshheading:11909735-Nitric Oxide Synthase,
pubmed-meshheading:11909735-Nitric Oxide Synthase Type II,
pubmed-meshheading:11909735-Protozoan Proteins,
pubmed-meshheading:11909735-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:11909735-Receptors, Tumor Necrosis Factor, Type I,
pubmed-meshheading:11909735-Toxoplasma,
pubmed-meshheading:11909735-Toxoplasmosis, Animal
|
pubmed:year |
2002
|
pubmed:articleTitle |
Toxoplasma gondii: in vivo expression of BAG-5 and cyst formation is independent of TNF p55 receptor and inducible nitric oxide synthase functions.
|
pubmed:affiliation |
Department of Biochemistry and Immunology, Federal University of Minas Gerais, Avenue Antônio Carlos 6627, Belo Horizonte, MG 31270-010, Brazil.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|