normal phenotype
• mice are phenotypically identical to wild-type controls and breed well
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Allele Symbol Allele Name Allele ID |
Arpc4tm1c(EUCOMM)Wtsi targeted mutation 1c, Wellcome Trust Sanger Institute MGI:6111539 |
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Summary |
2 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice are phenotypically identical to wild-type controls and breed well
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• molecular analysis revealed disrupted keratinocyte differentiation
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• at P7, hair follicles in psoriasis-like lesions often lack the sebaceous gland
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• at P1, local thickening of the epidermis, mainly the cornified layer, and scattered ghost (anucleated) cells are mostly evident in the head region
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• at P5, pups exhibit uneven skin thickening with alopecic areas
• at P7, hair follicles in psoriasis-like lesions often lack the shaft
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• at P5, body and extremities show poorly furred skin
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• at P7, hair follicles in psoriasis-like lesions are rare
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• at P7, the cornified layer is abnormally thickened
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• at P7, the thickened cornified layer is characterized by the presence of nuclei and microabscesses
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• at P7, the epidermal squamous cells exhibit hyperplasia (acanthosis)
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• at P1, local thickening of the epidermis, mainly the cornified layer, are mostly evident in the head region
• at P5, body and extremities show unevenly thickened skin
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• at P5, pups exhibit abnormal skin appearance with uneven thickening accompanied by alopecic areas
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• over time, psoriasis-like lesions acquire an ichthyosis-like appearance
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• initial skin lesions are detected microscopically at P1; mice have to be euthanized by P21 due to the severity of skin lesions
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• at P1, local thickening of the epidermis, mainly the cornified layer, and scattered ghost (anucleated) cells are mostly evident in the head region
• initial skin lesions develop progressively into macroscopic psoriasis-like plaques
• psoriasis-like lesions are variable in size and usually more severe in the dorsal than in the ventral trunk, extremities and head
• over time, psoriasis-like lesions acquire an ichthyosis-like appearance
• psoriatic epidermis exhibits hyperactivation of transcription factor Nrf2 and decreased F-actin levels
• however, mice do not exhibit any outside-in epidermal permeability barrier defects
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• skin lesions show increased Ki67 positivity in both the basal and the suprabasal epidermal layers
• at P4, the mutant epidermis shows increased nuclear Nrf2 levels; whereas the number of Nrf2-positive interfollicular keratinocytes declines with age in wild-type epidermis, Nrf2 expression remains ubiquitous in psoriasis-like lesions at P14, indicating Nrf2 hyperactivation
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• at P7, P14 and P21, inflammatory infiltrations mainly consisting of lymphocytic cells are detected in the dermis
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• molecular analysis revealed disrupted keratinocyte differentiation
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• at P7, hair follicles in psoriasis-like lesions often lack the sebaceous gland
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• at P1, local thickening of the epidermis, mainly the cornified layer, and scattered ghost (anucleated) cells are mostly evident in the head region
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• at P7, P14 and P21, inflammatory infiltrations mainly consisting of lymphocytic cells are detected in the dermis
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
psoriasis | DOID:8893 |
OMIM:PS177900 |
J:253986 |
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 |
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