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Phenotypes Associated with This Genotype
Genotype
MGI:6268445
Allelic
Composition
Tg(Tek-tTA)1Dmt/0
Tg(tetO-Tek)1Dmt/0
Genetic
Background
involves: CD-1
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
growth/size/body
• mice are on average 20-15% smaller than wild-type littermates

hematopoietic system
• mice exhibit increased numbers of eosinophils in the dermis
• expression of chemokines associated with eosinophil immune responses is increased in the blood and skin
• moderate increase in number of CD3+ T cells in the blood
• however, levels of B lymphocytes, myeloid cells, megakaryocytes, and erythrocytes in the blood are normal
• disruption of the normal red and white pulp architecture
• increase in infiltration of white blood cells such as myeloid cells and megakaryocytes in the red pulp
• disruption of the normal red and white pulp architecture

integument
• mice show focal dermal inflammatory infiltrates of mononuclear cells consisting primarily of lymphocytes with dispersed macrophages and mast cells (J:96718)
• some areas of skin in severely affected mice have aggregates of neutrophilic polymorphonuclear leukocytes that form microabscesses within the epidermis (J:96718)
• mice show an increase in the number of dermal mast cells and CD3+ T lymphocytes in the dermis (J:96718)
• mice exhibit increased numbers of eosinophils in the dermis (J:137745)
• emerging hair appears dull
• severely affected mice display patchy alopecia
• emerging hair appears sparse
• severely affected mice display yellow-brown discoloration of the nails
• in some regions of epidermal thickening, uneven elongation of structures resembling rete pegs extend downward into the dermis; these structures encompass hyperplastic hair follicles
• mice exhibit larger and more tortuous blood vessels immediately below the epidermis
• horizontal vessels comprising the subpapillary plexus and deeper cutaneous plexus are larger and often extend great distances in close proximity to the hyperproliferative epidermal layer
• increase in density and diameter of blood vessels in the skin, however no change in vessel numbers is seen
• mice treated with doxycycline show reduced vessel diameter and density in the dermis
• skin has an increased amount and density of cornified material, indicating compact hyperkeratosis
• skin has areas where nucleated cells are present in the cornified layer, indicating focal parakeratosis
• severely affected mice exhibit zones of hyperplasia due to variable increases in the number of cell layers in the squamous epithelium indicating acanthosis
• mild epidermal thickening in the skin of the ear, head, and back (J:96718)
• mice treated for 2 weeks with an anti-CD4 antibody do not show improved epidermal hyperplasia, indicating that maintenance of the skin disease is not dependent of CD4+ T lymphocytes (J:137745)
• beginning at P5, skin shows extensive erythema (J:96718)
• adults exhibit patches of thickened erythematous skin around the eyes, snout, ears, and other extensor surfaces including the knuckles of the legs and nape of the neck (J:96718)
• severity of erythema varies (J:96718)
• within 7 days of treating adult mice with doxycycline, mice show improved erythematous characteristics (J:96718)
• mice treated for 2 weeks with an anti-CD4 antibody show improved erythema (J:137745)
• beginning at P5, skin shows loosely adherent silver-white scaling
• skin is covered with focal areas of scaling that extend to the tail
• mice show increased genesis of skin lesions at sites of trauma that become large, thickened, and ulcerated
• skin shows features of psoriasis including epidermal hyperplasia, inflammatory cell accumulation and altered dermal angiogenesis
• within 4 days of doxycycline treatment beginning at P7, mice show improvements in skin and fur appearance
• severely affected mice treated with the immunosuppressive anti-psoriatic agent cyclosporine display improvement in skin phenotype, showing epidermal thinning, reduced dermal cellularity and vascular density

cardiovascular system
• dermis exhibits an increase in the number of blood capillaries with dilated and tortuous changes
• mice exhibit larger and more tortuous blood vessels immediately below the epidermis
• horizontal vessels comprising the subpapillary plexus and deeper cutaneous plexus are larger and often extend great distances in close proximity to the hyperproliferative epidermal layer
• increase in density and diameter of blood vessels in the skin, however no change in vessel numbers is seen
• mice treated with doxycycline show reduced vessel diameter and density in the dermis

immune system
• mice exhibit increased numbers of eosinophils in the dermis
• expression of chemokines associated with eosinophil immune responses is increased in the blood and skin
• moderate increase in number of CD3+ T cells in the blood
• however, levels of B lymphocytes, myeloid cells, megakaryocytes, and erythrocytes in the blood are normal
• disruption of the normal red and white pulp architecture
• increase in infiltration of white blood cells such as myeloid cells and megakaryocytes in the red pulp
• disruption of the normal red and white pulp architecture
• mice show focal dermal inflammatory infiltrates of mononuclear cells consisting primarily of lymphocytes with dispersed macrophages and mast cells (J:96718)
• some areas of skin in severely affected mice have aggregates of neutrophilic polymorphonuclear leukocytes that form microabscesses within the epidermis (J:96718)
• mice show an increase in the number of dermal mast cells and CD3+ T lymphocytes in the dermis (J:96718)
• mice exhibit increased numbers of eosinophils in the dermis (J:137745)

vision/eye
• older mice sporadically develop a white opacity of the eye indicating age-related cataract

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
psoriasis DOID:8893 OMIM:PS177900
J:96718


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
04/23/2024
MGI 6.23
The Jackson Laboratory