Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1.
Nicklas Heine StaunstrupKarin StenderupSidsel MortensenMaria Nascimento PrimoCecilia Rosada KjeldsenTorben SteinicheYing LiuRong LiMette SchmidtStig PurupFrederik Dagnæs-HansenLisbeth Dahl SchrøderLars SvenssonThomas Kongstad PetersenHenrik CallesenLars BolundJacob Giehm MikkelsenPublished in: Disease models & mechanisms (2018)
Psoriasis is a complex human-specific disease characterized by perturbed keratinocyte proliferation and a pro-inflammatory environment in the skin. Porcine skin architecture and immunity are very similar to that in humans, rendering the pig a suitable animal model for studying the biology and treatment of psoriasis. Expression of integrins, which is normally confined to the basal layer of the epidermis, is maintained in suprabasal keratinocytes in psoriatic skin, modulating proliferation and differentiation as well as leukocyte infiltration. Here, we generated minipigs co-expressing integrins α2 and β1 in suprabasal epidermal layers. Integrin-transgenic minipigs born into the project displayed skin phenotypes that correlated with the number of inserted transgenes. Molecular analyses were in good concordance with histological observations of psoriatic hallmarks, including hypogranulosis and T-lymphocyte infiltration. These findings mark the first creation of minipigs with a psoriasiform phenotype resembling human psoriasis and demonstrate that integrin signaling plays a key role in psoriasis pathology.
Keyphrases
- wound healing
- endothelial cells
- soft tissue
- poor prognosis
- induced pluripotent stem cells
- signaling pathway
- pluripotent stem cells
- disease activity
- ankylosing spondylitis
- peripheral blood
- atopic dermatitis
- systemic lupus erythematosus
- quality improvement
- preterm infants
- low birth weight
- smoking cessation
- preterm birth
- replacement therapy