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Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1

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 treatm...

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Autores principales: Staunstrup, Nicklas Heine, Stenderup, Karin, Mortensen, Sidsel, Primo, Maria Nascimento, Rosada, Cecilia, Steiniche, Torben, Liu, Ying, Li, Rong, Schmidt, Mette, Purup, Stig, Dagnæs-Hansen, Frederik, Schrøder, Lisbeth Dahl, Svensson, Lars, Petersen, Thomas Kongstad, Callesen, Henrik, Bolund, Lars, Mikkelsen, Jacob Giehm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536904/
https://www.ncbi.nlm.nih.gov/pubmed/28679670
http://dx.doi.org/10.1242/dmm.028662
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author Staunstrup, Nicklas Heine
Stenderup, Karin
Mortensen, Sidsel
Primo, Maria Nascimento
Rosada, Cecilia
Steiniche, Torben
Liu, Ying
Li, Rong
Schmidt, Mette
Purup, Stig
Dagnæs-Hansen, Frederik
Schrøder, Lisbeth Dahl
Svensson, Lars
Petersen, Thomas Kongstad
Callesen, Henrik
Bolund, Lars
Mikkelsen, Jacob Giehm
author_facet Staunstrup, Nicklas Heine
Stenderup, Karin
Mortensen, Sidsel
Primo, Maria Nascimento
Rosada, Cecilia
Steiniche, Torben
Liu, Ying
Li, Rong
Schmidt, Mette
Purup, Stig
Dagnæs-Hansen, Frederik
Schrøder, Lisbeth Dahl
Svensson, Lars
Petersen, Thomas Kongstad
Callesen, Henrik
Bolund, Lars
Mikkelsen, Jacob Giehm
author_sort Staunstrup, Nicklas Heine
collection PubMed
description 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.
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spelling pubmed-55369042017-08-10 Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1 Staunstrup, Nicklas Heine Stenderup, Karin Mortensen, Sidsel Primo, Maria Nascimento Rosada, Cecilia Steiniche, Torben Liu, Ying Li, Rong Schmidt, Mette Purup, Stig Dagnæs-Hansen, Frederik Schrøder, Lisbeth Dahl Svensson, Lars Petersen, Thomas Kongstad Callesen, Henrik Bolund, Lars Mikkelsen, Jacob Giehm Dis Model Mech Research Article 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. The Company of Biologists Ltd 2017-07-01 /pmc/articles/PMC5536904/ /pubmed/28679670 http://dx.doi.org/10.1242/dmm.028662 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Staunstrup, Nicklas Heine
Stenderup, Karin
Mortensen, Sidsel
Primo, Maria Nascimento
Rosada, Cecilia
Steiniche, Torben
Liu, Ying
Li, Rong
Schmidt, Mette
Purup, Stig
Dagnæs-Hansen, Frederik
Schrøder, Lisbeth Dahl
Svensson, Lars
Petersen, Thomas Kongstad
Callesen, Henrik
Bolund, Lars
Mikkelsen, Jacob Giehm
Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title_full Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title_fullStr Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title_full_unstemmed Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title_short Psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
title_sort psoriasiform skin disease in transgenic pigs with high-copy ectopic expression of human integrins α2 and β1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536904/
https://www.ncbi.nlm.nih.gov/pubmed/28679670
http://dx.doi.org/10.1242/dmm.028662
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