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同时暴露于紫外线A和香烟侧流烟雾下基质金属蛋白酶-1表达增加及组蛋白乙酰化的作用

Increased matrix metalloproteinase-1 expression by coexposure to UVA and cigarette sidestream smoke and contribution of histone acetylation.

作者信息

Ito Ryoma, Komaki Yukako, Ibuki Yuko

机构信息

Graduate Division of Nutritional and Environmental Sciences, University of Shizuoka, Yada 52- 1, Suruga-ku, Shizuoka, 422-8526, Japan.

出版信息

Genes Environ. 2025 Jan 26;47(1):2. doi: 10.1186/s41021-025-00325-z.

DOI:10.1186/s41021-025-00325-z
PMID:39865280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11765920/
Abstract

BACKGROUND

Skin is exposed to various environmental factors throughout life, and some of these factors are known to contribute to skin aging. Long-term solar UV exposure is a well-known cause of skin aging, as is cigarette smoke, which contains a number of chemicals. In this study, combined effect of UVA and cigarette sidestream smoke (CSS) on matrix metalloproteinase-1 (MMP-1) induction was investigated. MMP-1 is the main protease that initiates collagen type I fiber fragmentation in human skin and is associated with aging.

RESULTS

Combined exposure to UVA and CSS enhanced MMP-1 induction, accompanied by collagen type I (COL1A1) gene suppression. The basal expression of MMP-1 was higher in senescent cells than in normal cells, with a pronounced increase after coexposure to UVA and CSS. UVA irradiation resulted in global histone H3 acetylation, and we considered this was responsible for the MMP-1 upregulation. Histone deacetylase inhibitors, sodium acetate, propionate, and butyrate, all enhanced the CSS-induced MMP-1 according to the degree of histone acetylation.

CONCLUSION

These results suggest that UVA and CSS additively induce MMP-1, which may lead to skin aging, and that such combined effect may further promote aging in aged skin. UVA-induced histone acetylation may contribute to MMP-1 induction.

摘要

背景

皮肤在其整个生命周期中都会接触到各种环境因素,其中一些因素已知会导致皮肤老化。长期暴露于太阳紫外线是众所周知的皮肤老化原因,香烟烟雾也是如此,它含有多种化学物质。在本研究中,我们调查了紫外线A(UVA)和香烟侧流烟雾(CSS)对基质金属蛋白酶-1(MMP-1)诱导的联合作用。MMP-1是启动人类皮肤中I型胶原纤维断裂的主要蛋白酶,与皮肤老化相关。

结果

UVA和CSS联合暴露增强了MMP-1的诱导,同时伴有I型胶原(COL1A1)基因抑制。MMP-1的基础表达在衰老细胞中高于正常细胞,在UVA和CSS共同暴露后显著增加。UVA照射导致整体组蛋白H3乙酰化,我们认为这是MMP-1上调的原因。组蛋白脱乙酰酶抑制剂,醋酸钠、丙酸钠和丁酸钠,均根据组蛋白乙酰化程度增强了CSS诱导的MMP-1。

结论

这些结果表明,UVA和CSS可叠加诱导MMP-1,这可能导致皮肤老化,并且这种联合作用可能会进一步促进老年皮肤的老化。UVA诱导的组蛋白乙酰化可能有助于MMP-1的诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/693cc460a361/41021_2025_325_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/477fd5b30d20/41021_2025_325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f87a826111d3/41021_2025_325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f76e6d10d6e2/41021_2025_325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f9fa05b27655/41021_2025_325_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/693cc460a361/41021_2025_325_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/477fd5b30d20/41021_2025_325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f87a826111d3/41021_2025_325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f76e6d10d6e2/41021_2025_325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/f9fa05b27655/41021_2025_325_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6222/11765920/693cc460a361/41021_2025_325_Fig5_HTML.jpg

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本文引用的文献

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UVB-mediated DNA damage induces matrix metalloproteinases to promote photoaging in an AhR- and SP1-dependent manner.
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