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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cd4tm1(cre/ERT2)Thbu
targeted mutation 1, Thorsten Buch
MGI:5549971
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Cd4tm1(cre/ERT2)Thbu/Cd4+
Tgfbr2tm1Karl/Tgfbr2tm1Karl
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5550067
cn2
Cd4tm1(cre/ERT2)Thbu/Cd4+
Gfm1tm1c(EUCOMM)Wtsi/Gfm1tm1c(EUCOMM)Wtsi
involves: C57BL/6 * C57BL/6N * SJL MGI:6508531


Genotype
MGI:5550067
cn1
Allelic
Composition
Cd4tm1(cre/ERT2)Thbu/Cd4+
Tgfbr2tm1Karl/Tgfbr2tm1Karl
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd4tm1(cre/ERT2)Thbu mutation (0 available); any Cd4 mutation (85 available)
Tgfbr2tm1Karl mutation (1 available); any Tgfbr2 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• after 5 days of tamoxifen treatment, mice display no weight loss and appeared healthy at 2 and 4 weeks post-tamoxifen; no overt phenotype is observed 3 months following 2 months of tamoxifen treatment

immune system
N
• no cellular infiltrates (suggesting autoimmune responses) are detected in organs including liver, kidney, pancreas, heart, colon and thyroid gland from animals that received tamoxifen treatment
• no secondary effects on B cell tolerance indicated by autoantibody production are seen in mice at 6 weeks or 5 months after tamoxifen treatment
• at 2 and 4 weeks after tamoxifen treatment, mice show a modest but significant transient expansion of effector memory T cells in the spleen and lymph nodes; numbers and frequency of effector memory cells return to control levels at 6 weeks after tamoxifen administration as result of replacement with new T cells
• proliferation of effector memory T cells is increased without similar increase observed for naive T cells or central memory CD4+ T cells
• in mice thymectomized prior to tamoxifen treatment, elevation of effector memory T cells persists in absence of thymic emigration
• hyperproliferation of regulatory T cells is observed at 2 an 4 weeks after tamoxifen treatment; increased numbers are observed in lymph nodes, the spleen, the lung and Peyer's patches, but not in intestinal lamina propria

hematopoietic system
• at 2 and 4 weeks after tamoxifen treatment, mice show a modest but significant transient expansion of effector memory T cells in the spleen and lymph nodes; numbers and frequency of effector memory cells return to control levels at 6 weeks after tamoxifen administration as result of replacement with new T cells
• proliferation of effector memory T cells is increased without similar increase observed for naive T cells or central memory CD4+ T cells
• in mice thymectomized prior to tamoxifen treatment, elevation of effector memory T cells persists in absence of thymic emigration
• hyperproliferation of regulatory T cells is observed at 2 an 4 weeks after tamoxifen treatment; increased numbers are observed in lymph nodes, the spleen, the lung and Peyer's patches, but not in intestinal lamina propria




Genotype
MGI:6508531
cn2
Allelic
Composition
Cd4tm1(cre/ERT2)Thbu/Cd4+
Gfm1tm1c(EUCOMM)Wtsi/Gfm1tm1c(EUCOMM)Wtsi
Genetic
Background
involves: C57BL/6 * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd4tm1(cre/ERT2)Thbu mutation (0 available); any Cd4 mutation (85 available)
Gfm1tm1c(EUCOMM)Wtsi mutation (0 available); any Gfm1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• differentiation of tamoxifen-treated nave T cells under Th17 cell-skewing conditions yields a reduced frequency of IL-17 expressing cells
• tamoxifen-induced mice show a modest increase in the proportion of single-positive CD8+ population in the thymus
• tamoxifen-induced mice show a modest increase in the proportion of single-positive CD8+ population in the thymus
• tamoxifen-treated mice show significant protection from the development of experimental autoimmune encephalomyelitis (EAE), with mice showing lower numbers and percentages of MOG-specific IL-17 and IFN-gamma-producing Th cells in the central nervous system

hematopoietic system
• differentiation of tamoxifen-treated nave T cells under Th17 cell-skewing conditions yields a reduced frequency of IL-17 expressing cells
• tamoxifen-induced mice show a modest increase in the proportion of single-positive CD8+ population in the thymus
• tamoxifen-induced mice show a modest increase in the proportion of single-positive CD8+ population in the thymus





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory