Source:http://linkedlifedata.com/resource/pubmed/id/11115362
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2001-1-2
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pubmed:abstractText |
Immune complex formation was induced by the injection of (125)I-BSA into female MRL/Mp lpr/lpr mice, which develop spontaneous systemic lupus erythematosus (SLE)-like disease, and MRL/Mp +/+ mice, which do not. At designated intervals following the injection of 10 mg of (125)I-bovine serum albumin (BSA), the nonlupus mice developed sparse, small electron-dense deposits in mesangial areas and subepithelial immune deposits that underwent partial resolution. By contrast, glomeruli of the SLE-prone mouse kidneys revealed proliferation of mesangial cells and some increase in mesangial matrix material. Numerous subepithelial and mesangial electron-dense deposits were present. Some subendothelial and intramembranous deposits were also demonstrated. Capillary lumens contained massive electron-dense deposits. The resolving subepithelial deposits observed were fewer than half the number found in kidneys of the non-SLE mice. Whole body counts were also recorded daily following the injection of (125)I-BSA. Whereas, both lupus-prone and non-SLE control mice eliminated (125)I-BSA at equivalent rates through day 12 postinoculation, those with SLE-like disease showed a decreased (125)I-BSA elimination rate between days 6 and 12. Results suggest an impairment in the ability of SLE-prone mice to resolve immune complexes, whether they are nuclear-antinuclear or from an exogenous source, i.e., BSA-anti-BSA, compared to controls in this experimental model of the superimposition of exogenous immune complex formation on systemic lupus erythematosus-like disease.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0014-4800
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2000 Academic Press.
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pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
211-22
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:11115362-Animals,
pubmed-meshheading:11115362-Antigen-Antibody Complex,
pubmed-meshheading:11115362-Capillaries,
pubmed-meshheading:11115362-Disease Models, Animal,
pubmed-meshheading:11115362-Female,
pubmed-meshheading:11115362-Fluorescent Antibody Technique,
pubmed-meshheading:11115362-Glomerulonephritis,
pubmed-meshheading:11115362-Iodine Radioisotopes,
pubmed-meshheading:11115362-Kidney Glomerulus,
pubmed-meshheading:11115362-Lupus Erythematosus, Systemic,
pubmed-meshheading:11115362-Male,
pubmed-meshheading:11115362-Mice,
pubmed-meshheading:11115362-Mice, Inbred Strains,
pubmed-meshheading:11115362-Mice, Mutant Strains,
pubmed-meshheading:11115362-Microscopy, Electron,
pubmed-meshheading:11115362-Serum Albumin, Bovine,
pubmed-meshheading:11115362-Vasculitis
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pubmed:year |
2000
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pubmed:articleTitle |
Fate of immune complexes, glomerulonephritis, and cell-mediated vasculitis in lupus-prone MRL/Mp lpr/lpr mice.
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pubmed:affiliation |
Department of Pathology, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
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pubmed:publicationType |
Journal Article
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