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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(KRT14-VP16/NR1I2)13Sdub
transgene insertion 13, Sandrine Dubrac
MGI:6330734
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(KRT14-VP16/NR1I2)13Sdub/? involves: C57BL/6 MGI:6330737


Genotype
MGI:6330737
tg1
Allelic
Composition
Tg(KRT14-VP16/NR1I2)13Sdub/?
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• 10-16 week old mice exhibit increased transepidermal water loss associated with increased skin surface pH
• the cutaneous barrier defect precedes the development of the Th2/Th17 skin immune response
• mice exhibit Th2/Th17-mediated skin inflammation
• the cutaneous barrier defect precedes the development of the Th2/Th17 skin immune response
• skin microenvironment displays several key hallmarks of the immunological features seen in nonlesional atopic dermatitis
• epidermis shows increased proportions of short-chain fatty acids (NS 24:0-26:0), increased content of the lysophosphatidylcholine species 16:0 and 18:0, the phsopatidylcholine species with C32 and C34, and long and very long chain sphingomyelin lipid species
• skin exhibits mild-to-severe epidermal hyperplasia
• slight, but significant, epidermal thinning at birth that is accentuated 5 days after birth
• mice exhibit transient dry and scaly skin in the first days after birth
• however, mice do not exhibit gross skin abnormalities or scratching behavior at 10-16 weeks of age
• mice exhibit transient dry and scaly skin in the first days after birth

immune system
• the migration of skin-derived dendritic cells is increased, particularly migration of Langerhans cells and Langerin- dermal dendritic cells
• however, the number of Langerin+ dermal dendritic cells are not changed and numbers of plasmacytoid dendritic cells are borderline increased in skin draining lymph nodes
• all populations of skin dendritic cells are increased
• both CD4+ and CD8+ T-cell populations are enlarged in the skin of mice, with a specific increase in dermal T cells
• percentages of IL-17A-producing alpha/beta dermal T lymphocytes are increased
• increase in numbers of effector memory T cells (in both the CD4+ and CD8+ subsets) in skin draining lymph nodes
• proportions of CD45+ cells are increased in the skin and involve all leukocyte populations (lymphocytes, dendritic cells, and granulocytes such as eosinophils)
• peripheral blood shows increased percentages of leukocytes
• percentages of IL-13-producing epidermal TCRgamma/delta+ T cells are enhanced in the skin
• peripheral blood shows increased percentages of TCRgamma/delta+ T cells and the percentage of IL-13-producing TCRgamma/delta+ T cells is enhanced in the blood
• however, IL-17A-producing gamma/delta T lymphocytes are not changed and production of IFN-gamma, IL-2,and IL-10 remains very low and unchanged in T lymphocytes
• both CD4+ and CD8+ T-cell populations are enlarged in the skin of mice, with a specific increase in dermal T cells
• increase in basal levels of serum IgE
• 2.8-fold increase in levels of serum IgG1
• mice have slightly enlarged skin draining lymph nodes containing increased numbers of lymphocytes and activated CD4+ and CD8+ lymphocytes
• humoral Th2 immune response is triggered in the epidermis associated with increased serum IgE
• secretion of IL-1beta is abolished in keratinocytes
• mice exhibit Th2/Th17-mediated skin inflammation
• the cutaneous barrier defect precedes the development of the Th2/Th17 skin immune response
• skin microenvironment displays several key hallmarks of the immunological features seen in nonlesional atopic dermatitis
• type 2 innate lymphoid cells are increased in the skin

homeostasis/metabolism
• 10-16 week old mice exhibit increased transepidermal water loss associated with increased skin surface pH
• the cutaneous barrier defect precedes the development of the Th2/Th17 skin immune response
• skin surface pH is increased
• secretion of the growth factor GM-CSF is increased in keratinocytes

hematopoietic system
• the migration of skin-derived dendritic cells is increased, particularly migration of Langerhans cells and Langerin- dermal dendritic cells
• however, the number of Langerin+ dermal dendritic cells are not changed and numbers of plasmacytoid dendritic cells are borderline increased in skin draining lymph nodes
• all populations of skin dendritic cells are increased
• both CD4+ and CD8+ T-cell populations are enlarged in the skin of mice, with a specific increase in dermal T cells
• percentages of IL-17A-producing alpha/beta dermal T lymphocytes are increased
• increase in numbers of effector memory T cells (in both the CD4+ and CD8+ subsets) in skin draining lymph nodes
• proportions of CD45+ cells are increased in the skin and involve all leukocyte populations (lymphocytes, dendritic cells, and granulocytes such as eosinophils)
• peripheral blood shows increased percentages of leukocytes
• percentages of IL-13-producing epidermal TCRgamma/delta+ T cells are enhanced in the skin
• peripheral blood shows increased percentages of TCRgamma/delta+ T cells and the percentage of IL-13-producing TCRgamma/delta+ T cells is enhanced in the blood
• however, IL-17A-producing gamma/delta T lymphocytes are not changed and production of IFN-gamma, IL-2,and IL-10 remains very low and unchanged in T lymphocytes
• both CD4+ and CD8+ T-cell populations are enlarged in the skin of mice, with a specific increase in dermal T cells
• increase in basal levels of serum IgE
• 2.8-fold increase in levels of serum IgG1

cellular
• the migration of skin-derived dendritic cells is increased, particularly migration of Langerhans cells and Langerin- dermal dendritic cells
• however, the number of Langerin+ dermal dendritic cells are not changed and numbers of plasmacytoid dendritic cells are borderline increased in skin draining lymph nodes

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
atopic dermatitis DOID:3310 OMIM:603165
OMIM:PS603165
J:258435





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