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Metabolomics study of fibroblasts damaged by UVB and BaP

We have recently shown that both UVB and BaP can induce the production of ROS, apoptosis and even cancer. However, the differences in the metabolic profiles of skin damaged by UVB, BaP or UVB combined with BaP have not been studied. Therefore, we examined the metabolic changes in the human foreskin...

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Autores principales: Yang, Xiaoyu, Wang, Jiateng, Wang, Hecong, Li, Xueying, He, Congfen, Liu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160258/
https://www.ncbi.nlm.nih.gov/pubmed/34045475
http://dx.doi.org/10.1038/s41598-021-90186-7
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author Yang, Xiaoyu
Wang, Jiateng
Wang, Hecong
Li, Xueying
He, Congfen
Liu, Lei
author_facet Yang, Xiaoyu
Wang, Jiateng
Wang, Hecong
Li, Xueying
He, Congfen
Liu, Lei
author_sort Yang, Xiaoyu
collection PubMed
description We have recently shown that both UVB and BaP can induce the production of ROS, apoptosis and even cancer. However, the differences in the metabolic profiles of skin damaged by UVB, BaP or UVB combined with BaP have not been studied. Therefore, we examined the metabolic changes in the human foreskin fibroblast injured by UVB or BaP or the combination of the two, using ultra performance liquid chromatography (UPLC) coupled with quadrupole time-of-flight mass spectrometry (qTOF-MS). 24 metabolites were altered in the UVB damage group, 25 in the BaP damage group, and 33 in the UVB combined with BaP group. These alterations indicated that the metabolic mechanisms of HFF-1 cells treated with UVB or BaP are related to multiple main metabolites including glycerophosphocholine (PC), lactosylceramide (LacCer), guanidinosuccinic acid (GSA), glutathione(GSH), and lysophosphatidylcholine (LysoPC) and the main mechanisms involved glycerophospholipid and glutathione metabolism. Thus, our report provided useful insight into the underlying mechanisms of UVB and BaP damage to skin cells.
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spelling pubmed-81602582021-06-01 Metabolomics study of fibroblasts damaged by UVB and BaP Yang, Xiaoyu Wang, Jiateng Wang, Hecong Li, Xueying He, Congfen Liu, Lei Sci Rep Article We have recently shown that both UVB and BaP can induce the production of ROS, apoptosis and even cancer. However, the differences in the metabolic profiles of skin damaged by UVB, BaP or UVB combined with BaP have not been studied. Therefore, we examined the metabolic changes in the human foreskin fibroblast injured by UVB or BaP or the combination of the two, using ultra performance liquid chromatography (UPLC) coupled with quadrupole time-of-flight mass spectrometry (qTOF-MS). 24 metabolites were altered in the UVB damage group, 25 in the BaP damage group, and 33 in the UVB combined with BaP group. These alterations indicated that the metabolic mechanisms of HFF-1 cells treated with UVB or BaP are related to multiple main metabolites including glycerophosphocholine (PC), lactosylceramide (LacCer), guanidinosuccinic acid (GSA), glutathione(GSH), and lysophosphatidylcholine (LysoPC) and the main mechanisms involved glycerophospholipid and glutathione metabolism. Thus, our report provided useful insight into the underlying mechanisms of UVB and BaP damage to skin cells. Nature Publishing Group UK 2021-05-27 /pmc/articles/PMC8160258/ /pubmed/34045475 http://dx.doi.org/10.1038/s41598-021-90186-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Xiaoyu
Wang, Jiateng
Wang, Hecong
Li, Xueying
He, Congfen
Liu, Lei
Metabolomics study of fibroblasts damaged by UVB and BaP
title Metabolomics study of fibroblasts damaged by UVB and BaP
title_full Metabolomics study of fibroblasts damaged by UVB and BaP
title_fullStr Metabolomics study of fibroblasts damaged by UVB and BaP
title_full_unstemmed Metabolomics study of fibroblasts damaged by UVB and BaP
title_short Metabolomics study of fibroblasts damaged by UVB and BaP
title_sort metabolomics study of fibroblasts damaged by uvb and bap
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160258/
https://www.ncbi.nlm.nih.gov/pubmed/34045475
http://dx.doi.org/10.1038/s41598-021-90186-7
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