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Abnormal keratin expression pattern in prurigo nodularis epidermis

BACKGROUND: Prurigo nodularis (PN) is a highly pruritic, chronic dermatosis and difficult to treat. PN lesions are characterized by existence of many hyperkeratotic, erosive papules and nodules. However, the pathogenesis of PN still remains unelucidated. AIM: To clarify the keratin role in the epide...

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Autores principales: Yang, L. L., Jiang, B., Chen, S. H., Liu, H. Y., Chen, T. T., Huang, L. H., Yang, M., Ding, J., He, J. J., Li, J. J., Yu, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060049/
https://www.ncbi.nlm.nih.gov/pubmed/35665210
http://dx.doi.org/10.1002/ski2.75
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author Yang, L. L.
Jiang, B.
Chen, S. H.
Liu, H. Y.
Chen, T. T.
Huang, L. H.
Yang, M.
Ding, J.
He, J. J.
Li, J. J.
Yu, B.
author_facet Yang, L. L.
Jiang, B.
Chen, S. H.
Liu, H. Y.
Chen, T. T.
Huang, L. H.
Yang, M.
Ding, J.
He, J. J.
Li, J. J.
Yu, B.
author_sort Yang, L. L.
collection PubMed
description BACKGROUND: Prurigo nodularis (PN) is a highly pruritic, chronic dermatosis and difficult to treat. PN lesions are characterized by existence of many hyperkeratotic, erosive papules and nodules. However, the pathogenesis of PN still remains unelucidated. AIM: To clarify the keratin role in the epidermis hyperproliferation, the keratin expression pattern in the PN lesional skin. METHODS: In this study, we enrolled 24 patients with PN and 9 healthy control volunteers. K1/K10, K5/K14, K6/K16/K17 expression pattern were investigated by using immunohistochemical staining. RESULTS: The lesional skin consists of the thickened spinous layers, in which active cell division was found. K5/K14 were upregulated in PN lesional epidermis, the staining signal localized in the basal layer and lower suprabasal layers. Hyperproliferation‐associated K6 was found in all layers of epidermal lesional skin, especially in the spinous layers. In contrast, K16 was only detected in the basal and lower suprabasal layers, K17 was observed in the basal and spinous layers. Terminal differential keratins K1/K10 were upregulated, detected in the pan‐epidermis, but spared in the basal and low suprabasal layers. CONCLUSION: The keratinocytes enter an alternative differentiation pathway, which are responsible for the activated keratinocyte phenotype, abnormal keratins expression potentially contributes to the keratinocytes proliferation, subsequently lead to increased lesional skin epidermis thickness, hyperkeratiosis and alteration of skin barrier properties.
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spelling pubmed-90600492022-06-04 Abnormal keratin expression pattern in prurigo nodularis epidermis Yang, L. L. Jiang, B. Chen, S. H. Liu, H. Y. Chen, T. T. Huang, L. H. Yang, M. Ding, J. He, J. J. Li, J. J. Yu, B. Skin Health Dis Original Articles BACKGROUND: Prurigo nodularis (PN) is a highly pruritic, chronic dermatosis and difficult to treat. PN lesions are characterized by existence of many hyperkeratotic, erosive papules and nodules. However, the pathogenesis of PN still remains unelucidated. AIM: To clarify the keratin role in the epidermis hyperproliferation, the keratin expression pattern in the PN lesional skin. METHODS: In this study, we enrolled 24 patients with PN and 9 healthy control volunteers. K1/K10, K5/K14, K6/K16/K17 expression pattern were investigated by using immunohistochemical staining. RESULTS: The lesional skin consists of the thickened spinous layers, in which active cell division was found. K5/K14 were upregulated in PN lesional epidermis, the staining signal localized in the basal layer and lower suprabasal layers. Hyperproliferation‐associated K6 was found in all layers of epidermal lesional skin, especially in the spinous layers. In contrast, K16 was only detected in the basal and lower suprabasal layers, K17 was observed in the basal and spinous layers. Terminal differential keratins K1/K10 were upregulated, detected in the pan‐epidermis, but spared in the basal and low suprabasal layers. CONCLUSION: The keratinocytes enter an alternative differentiation pathway, which are responsible for the activated keratinocyte phenotype, abnormal keratins expression potentially contributes to the keratinocytes proliferation, subsequently lead to increased lesional skin epidermis thickness, hyperkeratiosis and alteration of skin barrier properties. John Wiley and Sons Inc. 2021-12-01 /pmc/articles/PMC9060049/ /pubmed/35665210 http://dx.doi.org/10.1002/ski2.75 Text en © 2021 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yang, L. L.
Jiang, B.
Chen, S. H.
Liu, H. Y.
Chen, T. T.
Huang, L. H.
Yang, M.
Ding, J.
He, J. J.
Li, J. J.
Yu, B.
Abnormal keratin expression pattern in prurigo nodularis epidermis
title Abnormal keratin expression pattern in prurigo nodularis epidermis
title_full Abnormal keratin expression pattern in prurigo nodularis epidermis
title_fullStr Abnormal keratin expression pattern in prurigo nodularis epidermis
title_full_unstemmed Abnormal keratin expression pattern in prurigo nodularis epidermis
title_short Abnormal keratin expression pattern in prurigo nodularis epidermis
title_sort abnormal keratin expression pattern in prurigo nodularis epidermis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060049/
https://www.ncbi.nlm.nih.gov/pubmed/35665210
http://dx.doi.org/10.1002/ski2.75
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