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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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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. |
format | Online Article Text |
id | pubmed-5536904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
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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