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Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy
Ultraviolet radiation is markedly increased because of pollution and the depletion of the stratospheric ozone layer. Excessive exposure to sunlight can negatively affect the skin, resulting in sunburn, photo-aging, or skin cancer. In this study, we first determined the photoprotective effect of sans...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325150/ https://www.ncbi.nlm.nih.gov/pubmed/30622245 http://dx.doi.org/10.1038/s41419-018-1261-y |
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author | Hao, Dan Wen, Xiang Liu, Lian Wang, Lian Zhou, Xianli Li, Yanmei Zeng, Xin He, Gu Jiang, Xian |
author_facet | Hao, Dan Wen, Xiang Liu, Lian Wang, Lian Zhou, Xianli Li, Yanmei Zeng, Xin He, Gu Jiang, Xian |
author_sort | Hao, Dan |
collection | PubMed |
description | Ultraviolet radiation is markedly increased because of pollution and the depletion of the stratospheric ozone layer. Excessive exposure to sunlight can negatively affect the skin, resulting in sunburn, photo-aging, or skin cancer. In this study, we first determined the photoprotective effect of sanshool, a major component in Zanthoxylum bungeanum, on UVB-irradiated responses in human dermal fibroblasts (HDFs) and nude mouse. We found that sanshool treatment can protect cells against the effects of UVB irradiation by (i) increasing cell viability, (ii) inhibiting MMP expression, and (iii) inducing autophagy. We also used the recombinant CSF2 or anti-CSF2 antibody co-cultured with human dermal fibroblasts (HDFs) and found that CSF2 contributes to sanshool-induced autophagy. Sanshool hindered the UVB-induced activation of JAK2-STAT3 signaling in HDFs, thereby inhibiting the expression of MMPs and activation of autophagic flux. Exposure of the dorsal skin of hairless mice to UVB radiation and subsequent topical application of sanshool delayed the progression of skin inflammation, leading to autophagy and inhibiting the activation of JAK2-STAT3 signaling. These results provide a basis for the study of the photoprotective effect of sanshool and suggest that it can be potentially used as an agent against UVB-induced skin damage in humans. |
format | Online Article Text |
id | pubmed-6325150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63251502019-01-09 Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy Hao, Dan Wen, Xiang Liu, Lian Wang, Lian Zhou, Xianli Li, Yanmei Zeng, Xin He, Gu Jiang, Xian Cell Death Dis Article Ultraviolet radiation is markedly increased because of pollution and the depletion of the stratospheric ozone layer. Excessive exposure to sunlight can negatively affect the skin, resulting in sunburn, photo-aging, or skin cancer. In this study, we first determined the photoprotective effect of sanshool, a major component in Zanthoxylum bungeanum, on UVB-irradiated responses in human dermal fibroblasts (HDFs) and nude mouse. We found that sanshool treatment can protect cells against the effects of UVB irradiation by (i) increasing cell viability, (ii) inhibiting MMP expression, and (iii) inducing autophagy. We also used the recombinant CSF2 or anti-CSF2 antibody co-cultured with human dermal fibroblasts (HDFs) and found that CSF2 contributes to sanshool-induced autophagy. Sanshool hindered the UVB-induced activation of JAK2-STAT3 signaling in HDFs, thereby inhibiting the expression of MMPs and activation of autophagic flux. Exposure of the dorsal skin of hairless mice to UVB radiation and subsequent topical application of sanshool delayed the progression of skin inflammation, leading to autophagy and inhibiting the activation of JAK2-STAT3 signaling. These results provide a basis for the study of the photoprotective effect of sanshool and suggest that it can be potentially used as an agent against UVB-induced skin damage in humans. Nature Publishing Group UK 2019-01-08 /pmc/articles/PMC6325150/ /pubmed/30622245 http://dx.doi.org/10.1038/s41419-018-1261-y 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 Hao, Dan Wen, Xiang Liu, Lian Wang, Lian Zhou, Xianli Li, Yanmei Zeng, Xin He, Gu Jiang, Xian Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title | Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title_full | Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title_fullStr | Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title_full_unstemmed | Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title_short | Sanshool improves UVB-induced skin photodamage by targeting JAK2/STAT3-dependent autophagy |
title_sort | sanshool improves uvb-induced skin photodamage by targeting jak2/stat3-dependent autophagy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325150/ https://www.ncbi.nlm.nih.gov/pubmed/30622245 http://dx.doi.org/10.1038/s41419-018-1261-y |
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