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Phenotypes Associated with This Genotype
Genotype
MGI:3760264
Allelic
Composition
Il2tm1Hor/Il2tm1Hor
Genetic
Background
B6.129P2-Il2tm1Hor/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il2tm1Hor mutation (5 available); any Il2 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• severe acinar gland destruction
• mild ductal changes in the salivary gland
• severe inflammation in the colon
• however, mice do show severe inflammation in the lung or the skin
• mice exhibit an increase in the lag time and a reduction of saliva production when treated with Pilocarpine, indicating loss of salivary gland function
• severe inflammation in the salivary glands
• major population of infiltrating leukocytes are lymphocytes and to a much lower extent neutrophils
• salivary glands show presence of a large fraction of T cells and a ratio of CD4+/CD8+ of 1/2
• although more Gr-1+ cells are seen in the salivary glands, the absolute number of neutrophils is relatively small

immune system
• severe inflammation in the colon
• however, mice do show severe inflammation in the lung or the skin
• severe inflammation in the salivary glands
• major population of infiltrating leukocytes are lymphocytes and to a much lower extent neutrophils
• salivary glands show presence of a large fraction of T cells and a ratio of CD4+/CD8+ of 1/2
• although more Gr-1+ cells are seen in the salivary glands, the absolute number of neutrophils is relatively small
• severe inflammation in the lacrimal glands
• there is a 2 to 5 fold reduction in the percentage of CD25-postive CD4 T cells in both the thymus and lymph nodes
• both CD4+ and CD8+ T cells fail to increase in size and granularity after activation with anti-CD3/28
• DNA replication fails to increase in activated CD4+ and CD8+ T cells after activation with anti-CD3/28
• after activation with anti-CD3/28
• after activation with anti-CD3/28
• after activation with anti-CD3/28
• increased cellularity of lymph nodes compared to wild-type mice, but lower than what is observed in Il2rbtm1Mak mice
• generalized symptoms of autoimmunity noted at 4 weeks of age
• transfer of wild-type regulatory T cells did not prevent autoimmune disorder
• wild-type regulatory T cells fail to engraft when adoptively transferred into these mice

endocrine/exocrine glands
• severe acinar gland destruction
• mild ductal changes in the salivary gland
• mice exhibit an increase in the lag time and a reduction of saliva production when treated with Pilocarpine, indicating loss of salivary gland function
• severe inflammation in the salivary glands
• major population of infiltrating leukocytes are lymphocytes and to a much lower extent neutrophils
• salivary glands show presence of a large fraction of T cells and a ratio of CD4+/CD8+ of 1/2
• although more Gr-1+ cells are seen in the salivary glands, the absolute number of neutrophils is relatively small
• severe inflammation in the lacrimal glands

cellular
• DNA replication fails to increase in activated CD4+ and CD8+ T cells after activation with anti-CD3/28
• fail to switch from oxidative phosphorylation to aerobic glycolysis after 5 days of tamoxifen treatment and activation with anti-CD3/28

vision/eye
• severe inflammation in the lacrimal glands

homeostasis/metabolism
• mice exhibit an increase in the lag time and a reduction of saliva production when treated with Pilocarpine, indicating loss of salivary gland function
• after activation with anti-CD3/28
• after activation with anti-CD3/28
• after activation with anti-CD3/28

hematopoietic system
• there is a 2 to 5 fold reduction in the percentage of CD25-postive CD4 T cells in both the thymus and lymph nodes
• both CD4+ and CD8+ T cells fail to increase in size and granularity after activation with anti-CD3/28
• DNA replication fails to increase in activated CD4+ and CD8+ T cells after activation with anti-CD3/28

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Sjogren's syndrome DOID:12894 OMIM:270150
J:125129


Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory