mortality/aging
• mice die before 20 months
|
immune system
• mice exhibit an increase in plasma cells in the blood, lymph node and spleen unlike wild-type mice
|
• from epidermal cells
|
• mice exhibit skin ulcerations, the lupus band in the epidermal-dermal junction, increased IL-6 secretion, mesangial hypercellularity with glomerular basement membrane thickening and luminal obstruction, small and strophic kidney, increased anti-histone antibodies, and decreased survival compared with wild-type mice
|
• UV-treated mice exhibit inflammatory perivascular infiltrates with abundant CD3+ T lymphocytes in the liver and lungs unlike similarly treated Junbtm3Wag homozygotes
• UV-treated mice develop swelling of the paws with functional articular impairment, synovial proliferation, and synovial membrane inflammation unlike similarly treated Junbtm3Wag homozygotes
|
• unlike wild-type controls, mice develop immunocomplex glomerulonephritis (IC-GN) characterized by mesangial hypercellularity, lobulation of the glomerular tuft with basement membrane thickening, endocapillary hypercellularity, and luminal obstruction by immuno complex deposits
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
|
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
|
dermatitis
(
J:155575
)
• starting at 3 months, mice exhibit dermatitis of ears, snouts, upper thorax region, and paws unlike wild-type mice
|
renal/urinary system
• mice display endocapillary hypercellularity and luminal obstruction by immuno complex deposits
|
• mice exhibit mesangial hypercellularity
|
albuminuria
(
J:155575
)
• unlike wild-type controls, mice develop immunocomplex glomerulonephritis (IC-GN) characterized by mesangial hypercellularity, lobulation of the glomerular tuft with basement membrane thickening, endocapillary hypercellularity, and luminal obstruction by immuno complex deposits
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
|
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
|
• mice exhibit podocyte foot process effacement in most glomerular capillary loops
|
• mice exhibit GBM thickening
|
• mice exhibit lobulation of the glomerular tuft
|
small kidney
(
J:155575
)
homeostasis/metabolism
albuminuria
(
J:155575
)
hematopoietic system
• mice exhibit an increase in plasma cells in the blood, lymph node and spleen unlike wild-type mice
|
integument
dermatitis
(
J:155575
)
• starting at 3 months, mice exhibit dermatitis of ears, snouts, upper thorax region, and paws unlike wild-type mice
|
• mice exhibit the lupus band in the epidermal-dermal junction unlike wild-type mice
|
• at 3 months
|
thick skin
(
J:155575
)
cardiovascular system
• mice display endocapillary hypercellularity and luminal obstruction by immuno complex deposits
|
cellular
• mice exhibit mesangial hypercellularity
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
systemic lupus erythematosus | DOID:9074 |
OMIM:152700 OMIM:300809 OMIM:605480 OMIM:608437 OMIM:609903 OMIM:609939 OMIM:610065 OMIM:610066 OMIM:612254 OMIM:612378 OMIM:613145 OMIM:614420 |
J:155575 |