immune system
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no females develop diabetes spontaneously over 5-7 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• no female mice develop insulitis between 5-7 months of age; a small number of male mice do display mild insulitis
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• no female mice develop insulitis between 5-7 months of age; a small number of male mice do display mild insulitis
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• animals show a significant reduction in overall diabetes incidence (14.6% vs ~50% in Tnfsf4-heterozygotes and wild-type) and increase in the age of onset (9.5 weeks vs 6 weeks in controls)
• mice are considered diabetic after a blood glucose measure of >300 mg/dl and 2 positive urine glucose tests
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• Background Sensitivity: although negative selection of these transgenic thymocytes is stronger on the B6 than NOD background, there is earlier onset and greater penetrance of diabetes in females on the B6 background
• Background Sensitivity: compared with those on the NOD background, on the B6 background these TCR transgenic T cells have greater proliferative response to antigen presentation and display more potent killing of pancreatic islet cells
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice develop diabetes (blood glucose >250 ml/dl) more rapidly than transgenic Rag1-null, Ins2-sufficient mice
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
type 1 diabetes mellitus | DOID:9744 |
OMIM:222100 |
J:111874 |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• 10-week-old diabetic mice show severe insulitis; disease is heterogeneous with some non-diabetic mice displaying it; infiltrate consists of CD4 cells, with an absence of CD8 T cells
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• 10-week-old diabetic mice show severe insulitis; disease is heterogeneous with some non-diabetic mice displaying it; infiltrate consists of CD4 cells, with an absence of CD8 T cells
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• 15% of mice heterozygous for H2g7 develop diabetes, compared to 50% of homozygous mice or 0% of non-H2g7 mice
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
type 1 diabetes mellitus | DOID:9744 |
OMIM:222100 |
J:111874 |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• insulitis is observed in some mice at 44 weeks but nor insulin autoantibodies are detected
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• insulitis is observed in some mice at 44 weeks but nor insulin autoantibodies are detected
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• transgenic Rag1-sufficient mice do not develop diabetes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• 15% of mice heterozygous for the H2 alleles develop diabetes by 44 weeks
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
type 1 diabetes mellitus | DOID:9744 |
OMIM:222100 |
J:111874 |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mitral valve inflammation begins at 3 weeks of age and by 8 weeks, accumulation of inflammatory cells and interstitial thickening is obvious indicating fibroinflammatory mitral valve disease
• mononuclear phagocytes (macrophages and monocytes) constitute the vast majority of accumulated leukocytes
• frequency of TNF- and IL-6-producing phagocytes in inflamed mitral valve tissue is elevated, indicating an enrichment of cytokine-producing phagocytes within the inflamed mitral valves
• antibody blockade of either TNF or IL-6 beginning at the onset of mitral valve inflammation reduces mitral valve fibrosis and thickening
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• rheumatoid arthritis occurs with disease onset transpiring between 25 and 35 days of age
(J:36815)
• arthritis occurrence is established by joint inspection and measure of ankle thickness, and histological confirmation in several mice
(J:36815)
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• mitral valve hydroxyproline content is elevated
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• by 8 weeks of age, mitral valves are fibrotic and thickened
• TNFR2 neutralization with a monoclonal antibody exacerbates mitral valve fibrosis and thickening
• blockade of either VLA-4 or VCAM-1 with monoclonal antibodies attenuates valve fibrosis and thickening
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• mitral valve inflammation begins at 3 weeks of age and by 8 weeks, accumulation of inflammatory cells and interstitial thickening is obvious indicating fibroinflammatory mitral valve disease
• mononuclear phagocytes (macrophages and monocytes) constitute the vast majority of accumulated leukocytes
• frequency of TNF- and IL-6-producing phagocytes in inflamed mitral valve tissue is elevated, indicating an enrichment of cytokine-producing phagocytes within the inflamed mitral valves
• antibody blockade of either TNF or IL-6 beginning at the onset of mitral valve inflammation reduces mitral valve fibrosis and thickening
|
• mitral valve hydroxyproline content is elevated
|
• rheumatoid arthritis occurs with disease onset transpiring between 25 and 35 days of age
(J:36815)
• arthritis occurrence is established by joint inspection and measure of ankle thickness, and histological confirmation in several mice
(J:36815)
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
mitral valve disease | DOID:61 | J:275827 | ||
rheumatoid arthritis | DOID:7148 |
OMIM:180300 |
J:36815 |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• in the pancreas
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• from CD4+ pancreatic T cells
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• from CD4+ pancreatic T cells
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• diabetes disease progression is abrogated compared to in control mice
• however, mice develop insulitis
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• in the pancreas
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/05/2024 MGI 6.24 |
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