hematopoietic system
• mice develop age-dependent splenomegaly
• 20% of mice greater than 1 year of age exhibit severe splenomegaly with partial to complete replacement of red and white pulp with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
• red and white pulp are often replaced with of red and white pulp with myelomonocytic cells that are often centers of extramedullary hematopoiesis
• myelomonocytic cells often accumulate in other organs and on the surface of the ears, tails and legs
|
• in cervical and inguinal lymph nodes and spleen
|
• in the peritoneum
|
• mice exhibit decreased platelet numbers that becomes more pronounced with age (at 6 to 8 weeks in peripheral blood, 1089+/-242 per ul compared to 609+/-207 per ul in wild-type mice; at 52 to 58 weeks in peripheral blood, 2540+/-1050 per ul compared to 1264+/-434 per ul in wild-type mice)
|
• red and white pulp are often replaced with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
• red and white pulp are often replaced with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
immune system
• mice develop age-dependent splenomegaly
• 20% of mice greater than 1 year of age exhibit severe splenomegaly with partial to complete replacement of red and white pulp with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
• in cervical and inguinal lymph nodes and spleen
|
• in the peritoneum
|
• mice exhibit decreased platelet numbers that becomes more pronounced with age (at 6 to 8 weeks in peripheral blood, 1089+/-242 per ul compared to 609+/-207 per ul in wild-type mice; at 52 to 58 weeks in peripheral blood, 2540+/-1050 per ul compared to 1264+/-434 per ul in wild-type mice)
|
• red and white pulp are often replaced with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
• red and white pulp are often replaced with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
• increased circulating immune complexes reactive to complement component 1 q
|
• basophils show high MHC II expression
|
• of IgE isotype
|
• of IgE isotype
|
homeostasis/metabolism
• increased circulating immune complexes reactive to complement component 1 q
|
albuminuria
(
J:161523
)
• elevated albumin-to-creatinine ratio
|
renal/urinary system
albuminuria
(
J:161523
)
• elevated albumin-to-creatinine ratio
|
growth/size/body
• mice develop age-dependent splenomegaly
• 20% of mice greater than 1 year of age exhibit severe splenomegaly with partial to complete replacement of red and white pulp with myelomonocytic cells that are often centers of extramedullary hematopoiesis
|
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:161523 |