immune system
| N |
• unlike in mutant mice wild-type for Tcra, massive lymphadenopathy is not seen at 16 weeks of age
|
|
• 6 fold increase in TCRB+ cells compared to mutant mice wild-type for Fas
• within the TCRB+ cell population the proportion of DN B220+ cells is increased compared mutant mice wild-type for Fas
|
|
• 15 fold expansion at 16 weeks of age compared to mutant mice wild-type for Fas
• the majority of these cells express B220 and DN as a result of preferential expansion (300 fold) of this population of cells
|
|
• increase in the proportion of T cells in the peripheral lymph nodes expressing the gamma delta variable regions typical of intestinal intraepithelial T cell compared to mutant mice wild-type for Fas
|
|
• periglomerular infiltration and perivasculitis
|
renal/urinary system
|
• compared to age-matched B10.A mice
|
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• periglomerular infiltration and perivasculitis
|
|
• develop glomerular, interstitial and sometimes perivascular lesions
• lesion development is reduced compared mutant mice wild-type for Tcra
|
|
• focal glomerular hypercellularity
|
homeostasis/metabolism
|
• significantly elevated
|
|
• compared to age-matched B10.A mice
|
hematopoietic system
|
• 6 fold increase in TCRB+ cells compared to mutant mice wild-type for Fas
• within the TCRB+ cell population the proportion of DN B220+ cells is increased compared mutant mice wild-type for Fas
|
|
• 15 fold expansion at 16 weeks of age compared to mutant mice wild-type for Fas
• the majority of these cells express B220 and DN as a result of preferential expansion (300 fold) of this population of cells
|
|
• increase in the proportion of T cells in the peripheral lymph nodes expressing the gamma delta variable regions typical of intestinal intraepithelial T cell compared to mutant mice wild-type for Fas
|


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