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Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis

BACKGROUND: Psoriasis is a chronic inflammatory skin disease. The etiology of psoriasis is not fully understood, but the genetic background is considered to be the most important factor. To date, many psoriasis-related genes have been discovered, but the role of many important genes has not been wel...

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Autores principales: Hong, Dong-Kyun, Choi, Mi-Ra, Hwang, Yul-Lye, Lee, Jae Kyung, Lee, Young, Seo, Young-Joon, Kim, Sooil, Lee, Young-Ho, Kim, Chang-Deok, Lee, Jeung-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273324/
https://www.ncbi.nlm.nih.gov/pubmed/34341635
http://dx.doi.org/10.5021/ad.2021.33.4.339
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author Hong, Dong-Kyun
Choi, Mi-Ra
Hwang, Yul-Lye
Lee, Jae Kyung
Lee, Young
Seo, Young-Joon
Kim, Sooil
Lee, Young-Ho
Kim, Chang-Deok
Lee, Jeung-Hoon
author_facet Hong, Dong-Kyun
Choi, Mi-Ra
Hwang, Yul-Lye
Lee, Jae Kyung
Lee, Young
Seo, Young-Joon
Kim, Sooil
Lee, Young-Ho
Kim, Chang-Deok
Lee, Jeung-Hoon
author_sort Hong, Dong-Kyun
collection PubMed
description BACKGROUND: Psoriasis is a chronic inflammatory skin disease. The etiology of psoriasis is not fully understood, but the genetic background is considered to be the most important factor. To date, many psoriasis-related genes have been discovered, but the role of many important genes has not been well understood. OBJECTIVE: The purpose of this study is to uncover possible roles of MDA5 in psoriasis. METHODS: Expression of MDA5 was investigated using immunohistochemistry. Then, MDA5 was overexpressed in keratinocytes using a recombinant adenovirus. RESULTS: As a result of immunohistochemical staining, the expression of MDA5 was significantly increased in the epidermis of psoriasis compared to normal skin. Similarly, the expression of MDA5 was increased in imiquimod-induced psoriasiform dermatitis model. In cultured keratinocytes, toll-like receptor 3 agonist poly(I:C) induced expression of MDA5 at both mRNA and protein levels. When MDA5 was overexpressed using a recombinant adenovirus, poly(I:C)-induced cytokine expression was significantly increased. Finally, MDA5 overexpression significantly inhibited calcium-induced differentiation of keratinocytes. CONCLUSION: These results suggest that MDA5 increases in psoriasis and negatively regulates keratinocyte differentiation.
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spelling pubmed-82733242021-08-01 Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis Hong, Dong-Kyun Choi, Mi-Ra Hwang, Yul-Lye Lee, Jae Kyung Lee, Young Seo, Young-Joon Kim, Sooil Lee, Young-Ho Kim, Chang-Deok Lee, Jeung-Hoon Ann Dermatol Original Article BACKGROUND: Psoriasis is a chronic inflammatory skin disease. The etiology of psoriasis is not fully understood, but the genetic background is considered to be the most important factor. To date, many psoriasis-related genes have been discovered, but the role of many important genes has not been well understood. OBJECTIVE: The purpose of this study is to uncover possible roles of MDA5 in psoriasis. METHODS: Expression of MDA5 was investigated using immunohistochemistry. Then, MDA5 was overexpressed in keratinocytes using a recombinant adenovirus. RESULTS: As a result of immunohistochemical staining, the expression of MDA5 was significantly increased in the epidermis of psoriasis compared to normal skin. Similarly, the expression of MDA5 was increased in imiquimod-induced psoriasiform dermatitis model. In cultured keratinocytes, toll-like receptor 3 agonist poly(I:C) induced expression of MDA5 at both mRNA and protein levels. When MDA5 was overexpressed using a recombinant adenovirus, poly(I:C)-induced cytokine expression was significantly increased. Finally, MDA5 overexpression significantly inhibited calcium-induced differentiation of keratinocytes. CONCLUSION: These results suggest that MDA5 increases in psoriasis and negatively regulates keratinocyte differentiation. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2021-08 2021-07-01 /pmc/articles/PMC8273324/ /pubmed/34341635 http://dx.doi.org/10.5021/ad.2021.33.4.339 Text en Copyright © 2021 The Korean Dermatological Association and The Korean Society for Investigative Dermatology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hong, Dong-Kyun
Choi, Mi-Ra
Hwang, Yul-Lye
Lee, Jae Kyung
Lee, Young
Seo, Young-Joon
Kim, Sooil
Lee, Young-Ho
Kim, Chang-Deok
Lee, Jeung-Hoon
Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title_full Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title_fullStr Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title_full_unstemmed Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title_short Potential Role of Cytosolic RNA Sensor MDA5 as an Inhibitor for Keratinocyte Differentiation in the Pathogenesis of Psoriasis
title_sort potential role of cytosolic rna sensor mda5 as an inhibitor for keratinocyte differentiation in the pathogenesis of psoriasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273324/
https://www.ncbi.nlm.nih.gov/pubmed/34341635
http://dx.doi.org/10.5021/ad.2021.33.4.339
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