Metabolomics study of fibroblasts damaged by UVB and BaP

Abstract 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...

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Autores principales: Xiaoyu Yang, Jiateng Wang, Hecong Wang, Xueying Li, Congfen He, Lei Liu
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:082892cd81e445ac8703c444149c24932021-12-02T14:49:24ZMetabolomics study of fibroblasts damaged by UVB and BaP10.1038/s41598-021-90186-72045-2322https://doaj.org/article/082892cd81e445ac8703c444149c24932021-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-90186-7https://doaj.org/toc/2045-2322Abstract 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.Xiaoyu YangJiateng WangHecong WangXueying LiCongfen HeLei LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiaoyu Yang
Jiateng Wang
Hecong Wang
Xueying Li
Congfen He
Lei Liu
Metabolomics study of fibroblasts damaged by UVB and BaP
description Abstract 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.
format article
author Xiaoyu Yang
Jiateng Wang
Hecong Wang
Xueying Li
Congfen He
Lei Liu
author_facet Xiaoyu Yang
Jiateng Wang
Hecong Wang
Xueying Li
Congfen He
Lei Liu
author_sort Xiaoyu Yang
title Metabolomics study of fibroblasts damaged by UVB and BaP
title_short 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_sort metabolomics study of fibroblasts damaged by uvb and bap
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/082892cd81e445ac8703c444149c2493
work_keys_str_mv AT xiaoyuyang metabolomicsstudyoffibroblastsdamagedbyuvbandbap
AT jiatengwang metabolomicsstudyoffibroblastsdamagedbyuvbandbap
AT hecongwang metabolomicsstudyoffibroblastsdamagedbyuvbandbap
AT xueyingli metabolomicsstudyoffibroblastsdamagedbyuvbandbap
AT congfenhe metabolomicsstudyoffibroblastsdamagedbyuvbandbap
AT leiliu metabolomicsstudyoffibroblastsdamagedbyuvbandbap
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