immune system
N |
• T cell numbers in lymph nodes are normal
(J:73100)
• dendritic cells show normal function in mutants
(J:118565)
|
• a transitional block in early B cell development in evident in bone marrow; pre-B cells are decreased in number
|
• numbers of CD11c+ dendritic cells (DCs) are reduced in mutants
|
• numbers are reduced 3-fold in spleen vs wild-type
(J:73100)
• there are 5- to 40-fold fewer antigen specific CD4 cells producing Il-2 in mutants compared to controls 6 months after keyhole limpet hemocyanin immunization
(J:118565)
|
• numbers are reduced 3-fold in spleen vs wild-type
|
• in mutants, area of T zone stromal cell network in the spleen is decreased four- to five-fold compared to wild-type
• T zone cross sectional area is decreased 2- to 3-fold
|
• spleens are ~50% the weight of wild-type spleens
|
• mice fail to respond to T cell-dependent (OVA) or T cell-independent (dextra) antigenic stimulation and do not produce serum specific antibodies to these antigens
|
• null mice have almost undetectable serum levels of IgG1, IgG2a, IgG2b, IgG3, IgM and IgA compared to wild-type controls or Faslpr mice
|
• IgE is not detectable in serum of OVA-treated mutants, but high levels are produced in treated wild-type
|
• IgG levels drop rapidly after birth due to loss of maternal Ig
(J:119584)
• IgG is not detectable in OVA-treated mutants, but high levels are produced in treated wild-type
(J:125656)
|
• IgG1 is not detected in serum after OVA challenge
|
• in mutants, Il-2 secretion is diminished from T cells primed in absence of B cells compared to controls 6 months after keyhole limpet hemocyanin immunization
|
• mice fail to clear a Giardia muris infection
• two weeks after Giardia infection, there are 10-fold more Giardia cysts present in the feces of mice
• mice have 10-fold more Giardia trophozoites in the small intestine three weeks after infection and a thousand-fold more 7 weeks after infection compared to controls
• mutant mice still have an active Giardia population in the gut one year after infection while wild-type mice clear Giardia after about 7 weeks
• mice are not protected from Giardia upon a secondary challenge as wild-type mice are
|
hematopoietic system
• a transitional block in early B cell development in evident in bone marrow; pre-B cells are decreased in number
|
• numbers of CD11c+ dendritic cells (DCs) are reduced in mutants
|
• numbers are reduced 3-fold in spleen vs wild-type
(J:73100)
• there are 5- to 40-fold fewer antigen specific CD4 cells producing Il-2 in mutants compared to controls 6 months after keyhole limpet hemocyanin immunization
(J:118565)
|
• numbers are reduced 3-fold in spleen vs wild-type
|
• in mutants, area of T zone stromal cell network in the spleen is decreased four- to five-fold compared to wild-type
• T zone cross sectional area is decreased 2- to 3-fold
|
• spleens are ~50% the weight of wild-type spleens
|
• null mice have almost undetectable serum levels of IgG1, IgG2a, IgG2b, IgG3, IgM and IgA compared to wild-type controls or Faslpr mice
|
• IgE is not detectable in serum of OVA-treated mutants, but high levels are produced in treated wild-type
|
• IgG levels drop rapidly after birth due to loss of maternal Ig
(J:119584)
• IgG is not detectable in OVA-treated mutants, but high levels are produced in treated wild-type
(J:125656)
|
• IgG1 is not detected in serum after OVA challenge
|
respiratory system
• ovalbumin-sensitized/challenged mice (OVA) are unable to generate an early phase reaction (EPR- initial phase of brochoconstriction) following OVA provocation
|
cardiovascular system
• mutants are protected from developing elastase-induced abdominal aortic aneurysm
|
homeostasis/metabolism
• mutants are protected from developing elastase-induced abdominal aortic aneurysm
• reconstitution of mutants with mouse natural antibodies from pooled sera of wild-type mice does not restore susceptibility to abdominal aortic aneurysm in mutants, however reconstitution with pooled mouse IgG to the wild-type level renders mutants susceptible to abdominal aortic aneurysm
|
skeleton
• significantly decreased at 10 weeks of age
|
• reduced trabecular bone structure in femora
• reduced number of trabeculae
|