Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis

Abstract Matrix metalloproteinase13 (MMP13) can be released by keratinocytes and fibroblasts and involved in the pathogenesis of skin disorders. Retinoic acid derivative drugs include tazarotene and acitretin. Tazarotene/acitretin and narrow-band ultraviolet B (NB-UVB) irradiation are common treatme...

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Autores principales: Chan Xi, Chuanxi Xiong, Huiping Wang, Yuanjun Liu, Suju Luo
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/c0e55550661a48d2bf8c016d9d55a65d
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spelling oai:doaj.org-article:c0e55550661a48d2bf8c016d9d55a65d2021-12-02T18:02:49ZCombination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis10.1038/s41598-021-92599-w2045-2322https://doaj.org/article/c0e55550661a48d2bf8c016d9d55a65d2021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-92599-whttps://doaj.org/toc/2045-2322Abstract Matrix metalloproteinase13 (MMP13) can be released by keratinocytes and fibroblasts and involved in the pathogenesis of skin disorders. Retinoic acid derivative drugs include tazarotene and acitretin. Tazarotene/acitretin and narrow-band ultraviolet B (NB-UVB) irradiation are common treatment options for psoriasis. However, their impact on MMP13 expression in the context of psoriasis has yet to be determined. The expression of MMP13 was analyzed in patients with psoriasis. The effects of tazarotene/acitretin and NB-UVB on MMP13 expression were also investigated in a mouse model of psoriasis. Human HaCaT keratinocytes were exposed to acitretin or NB-UVB and then assayed for cell proliferation and MMP13 expression levels. We showed that patients with psoriasis had increased levels of MMP13 protein in skin lesions and serum samples. Exposure to acitretin and NB-UVB irradiation alone or in combination led to reduction of cell proliferation and MMP13 expression in HaCaT cells. Consistently, tazarotene treatment or NB-UVB irradiation attenuated imiquimod-induced psoriasis-like dermatitis and decreased MMP13 expression in a mouse model. Based on these from HaCaT keratinocytes cells and animal experiments, we suggest that tazarotene/acitretin and NB-UVB irradiation can inhibit the expression of MMP13 in HaCaT keratinocytes and psoriasis mouse models. Blockade of MMP13 activity may have therapeutic potential in improving symptoms of psoriasis.Chan XiChuanxi XiongHuiping WangYuanjun LiuSuju LuoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Chan Xi
Chuanxi Xiong
Huiping Wang
Yuanjun Liu
Suju Luo
Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
description Abstract Matrix metalloproteinase13 (MMP13) can be released by keratinocytes and fibroblasts and involved in the pathogenesis of skin disorders. Retinoic acid derivative drugs include tazarotene and acitretin. Tazarotene/acitretin and narrow-band ultraviolet B (NB-UVB) irradiation are common treatment options for psoriasis. However, their impact on MMP13 expression in the context of psoriasis has yet to be determined. The expression of MMP13 was analyzed in patients with psoriasis. The effects of tazarotene/acitretin and NB-UVB on MMP13 expression were also investigated in a mouse model of psoriasis. Human HaCaT keratinocytes were exposed to acitretin or NB-UVB and then assayed for cell proliferation and MMP13 expression levels. We showed that patients with psoriasis had increased levels of MMP13 protein in skin lesions and serum samples. Exposure to acitretin and NB-UVB irradiation alone or in combination led to reduction of cell proliferation and MMP13 expression in HaCaT cells. Consistently, tazarotene treatment or NB-UVB irradiation attenuated imiquimod-induced psoriasis-like dermatitis and decreased MMP13 expression in a mouse model. Based on these from HaCaT keratinocytes cells and animal experiments, we suggest that tazarotene/acitretin and NB-UVB irradiation can inhibit the expression of MMP13 in HaCaT keratinocytes and psoriasis mouse models. Blockade of MMP13 activity may have therapeutic potential in improving symptoms of psoriasis.
format article
author Chan Xi
Chuanxi Xiong
Huiping Wang
Yuanjun Liu
Suju Luo
author_facet Chan Xi
Chuanxi Xiong
Huiping Wang
Yuanjun Liu
Suju Luo
author_sort Chan Xi
title Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
title_short Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
title_full Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
title_fullStr Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
title_full_unstemmed Combination of retinoids and narrow-band ultraviolet B inhibits matrix metalloproteinase 13 expression in HaCaT keratinocytes and a mouse model of psoriasis
title_sort combination of retinoids and narrow-band ultraviolet b inhibits matrix metalloproteinase 13 expression in hacat keratinocytes and a mouse model of psoriasis
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c0e55550661a48d2bf8c016d9d55a65d
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AT huipingwang combinationofretinoidsandnarrowbandultravioletbinhibitsmatrixmetalloproteinase13expressioninhacatkeratinocytesandamousemodelofpsoriasis
AT yuanjunliu combinationofretinoidsandnarrowbandultravioletbinhibitsmatrixmetalloproteinase13expressioninhacatkeratinocytesandamousemodelofpsoriasis
AT sujuluo combinationofretinoidsandnarrowbandultravioletbinhibitsmatrixmetalloproteinase13expressioninhacatkeratinocytesandamousemodelofpsoriasis
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