mortality/aging
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• mice become moribund and are sacrificed at 4 months mutants posttransfer of Ifng wild-type F4/80+ macrophages at 2 months while all controls remain alive
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immune system
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• macrophage accumulation is reduced compared to Faslpr homozygotes
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• mice develop glomerular autoantibody deposits, but do not develop glomerulonephritis
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• mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months develop diffuse proliferative glomerulonephritis by 6 months
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renal/urinary system
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• glomeruli are hypercellular in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
• glomerular damage is more severe in mice receiving cell transfer than in control mice not receiving transfers
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• thickening of capillary walls in glomeruli is observed in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
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• mesangial cells are increased in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
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• mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months develop diffuse proliferative glomerulonephritis by 6 months
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homeostasis/metabolism
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• BUN levels are elevated at time of death in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
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cardiovascular system
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• thickening of capillary walls in glomeruli is observed in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
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cellular
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• mesangial cells are increased in mutants receiving adoptive transfer of Ifng wild-type F4/80+ macrophages at 2 months
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• macrophage accumulation is reduced compared to Faslpr homozygotes
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hematopoietic system
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• macrophage accumulation is reduced compared to Faslpr homozygotes
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