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C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes
Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988722/ https://www.ncbi.nlm.nih.gov/pubmed/29872130 http://dx.doi.org/10.1038/s41598-018-26996-z |
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author | Chen, Caifeng Wu, Na Duan, Qiqi Yang, Huizi Wang, Xin Yang, Peiwen Zhang, Mengdi Liu, Jiankang Liu, Zhi Shao, Yongping Zheng, Yan |
author_facet | Chen, Caifeng Wu, Na Duan, Qiqi Yang, Huizi Wang, Xin Yang, Peiwen Zhang, Mengdi Liu, Jiankang Liu, Zhi Shao, Yongping Zheng, Yan |
author_sort | Chen, Caifeng |
collection | PubMed |
description | Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment. |
format | Online Article Text |
id | pubmed-5988722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59887222018-06-20 C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes Chen, Caifeng Wu, Na Duan, Qiqi Yang, Huizi Wang, Xin Yang, Peiwen Zhang, Mengdi Liu, Jiankang Liu, Zhi Shao, Yongping Zheng, Yan Sci Rep Article Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment. Nature Publishing Group UK 2018-06-05 /pmc/articles/PMC5988722/ /pubmed/29872130 http://dx.doi.org/10.1038/s41598-018-26996-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Caifeng Wu, Na Duan, Qiqi Yang, Huizi Wang, Xin Yang, Peiwen Zhang, Mengdi Liu, Jiankang Liu, Zhi Shao, Yongping Zheng, Yan C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title_full | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title_fullStr | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title_full_unstemmed | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title_short | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
title_sort | c10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988722/ https://www.ncbi.nlm.nih.gov/pubmed/29872130 http://dx.doi.org/10.1038/s41598-018-26996-z |
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