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Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)

Xeroderma Pigmentosum (XP) is a DNA repair disease characterized by nucleotide excision repair (NER) malfunction, leading to photosensitivity and increased incidence of skin malignancies. The role of XP-A in NER pathways has been well studied while discrepancies associated with ROS levels and the ro...

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Autores principales: Krokidis, Marios G., Parlanti, Eleonora, D’Errico, Mariarosaria, Pascucci, Barbara, Pino, Anna, Alimonti, Alessandro, Pietraforte, Donatella, Masi, Annalisa, Ferreri, Carla, Chatgilialoglu, Chryssostomos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912421/
https://www.ncbi.nlm.nih.gov/pubmed/31683970
http://dx.doi.org/10.3390/cells8111377
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author Krokidis, Marios G.
Parlanti, Eleonora
D’Errico, Mariarosaria
Pascucci, Barbara
Pino, Anna
Alimonti, Alessandro
Pietraforte, Donatella
Masi, Annalisa
Ferreri, Carla
Chatgilialoglu, Chryssostomos
author_facet Krokidis, Marios G.
Parlanti, Eleonora
D’Errico, Mariarosaria
Pascucci, Barbara
Pino, Anna
Alimonti, Alessandro
Pietraforte, Donatella
Masi, Annalisa
Ferreri, Carla
Chatgilialoglu, Chryssostomos
author_sort Krokidis, Marios G.
collection PubMed
description Xeroderma Pigmentosum (XP) is a DNA repair disease characterized by nucleotide excision repair (NER) malfunction, leading to photosensitivity and increased incidence of skin malignancies. The role of XP-A in NER pathways has been well studied while discrepancies associated with ROS levels and the role of radical species between normal and deficient XPA cell lines have been observed. Using liquid chromatography tandem mass spectrometry we have determined the four 5’,8-cyclopurines (cPu) lesions (i.e., 5′R-cdG, 5′S-cdG, 5′R-cdA and 5′S-cdA), 8-oxo-dA and 8-oxo-dG in wt (EUE-pBD650) and XPA-deficient (EUE-siXPA) human embryonic epithelial cell lines, under different oxygen tension (hyperoxic 21%, physioxic 5% and hypoxic 1%). The levels of Fe and Cu were also measured. The main findings of our study were: (i) the total amount of cPu (1.82–2.52 lesions/10(6) nucleotides) is the same order of magnitude as 8-oxo-Pu (3.10–4.11 lesions/10(6) nucleotides) in both cell types, (ii) the four cPu levels are similar in hyperoxic and physioxic conditions for both wt and deficient cell lines, whereas 8-oxo-Pu increases in all cases, (iii) both wt and deficient cell lines accumulated high levels of cPu under hypoxic compared to physioxic conditions, whereas the 8-oxo-Pu levels show an opposite trend, (iv) the diastereoisomeric ratios 5′R/5′S are independent of oxygen concentration being 0.29 for cdG and 2.69 for cdA for EUE-pBD650 (wt) and 0.32 for cdG and 2.94 for cdA for EUE-siXPA (deficient), (v) in deficient cell lines Fe levels were significantly higher. The data show for the first time the connection of oxygen concentration in cells with different DNA repair ability and the levels of different DNA lesions highlighting the significance of cPu. Membrane lipidomic data at 21% O(2) indicated differences in the fatty acid contents between wild type and deficient cells, envisaging functional effects on membranes associated with the different repair capabilities, to be further investigated.
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spelling pubmed-69124212020-01-02 Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA) Krokidis, Marios G. Parlanti, Eleonora D’Errico, Mariarosaria Pascucci, Barbara Pino, Anna Alimonti, Alessandro Pietraforte, Donatella Masi, Annalisa Ferreri, Carla Chatgilialoglu, Chryssostomos Cells Article Xeroderma Pigmentosum (XP) is a DNA repair disease characterized by nucleotide excision repair (NER) malfunction, leading to photosensitivity and increased incidence of skin malignancies. The role of XP-A in NER pathways has been well studied while discrepancies associated with ROS levels and the role of radical species between normal and deficient XPA cell lines have been observed. Using liquid chromatography tandem mass spectrometry we have determined the four 5’,8-cyclopurines (cPu) lesions (i.e., 5′R-cdG, 5′S-cdG, 5′R-cdA and 5′S-cdA), 8-oxo-dA and 8-oxo-dG in wt (EUE-pBD650) and XPA-deficient (EUE-siXPA) human embryonic epithelial cell lines, under different oxygen tension (hyperoxic 21%, physioxic 5% and hypoxic 1%). The levels of Fe and Cu were also measured. The main findings of our study were: (i) the total amount of cPu (1.82–2.52 lesions/10(6) nucleotides) is the same order of magnitude as 8-oxo-Pu (3.10–4.11 lesions/10(6) nucleotides) in both cell types, (ii) the four cPu levels are similar in hyperoxic and physioxic conditions for both wt and deficient cell lines, whereas 8-oxo-Pu increases in all cases, (iii) both wt and deficient cell lines accumulated high levels of cPu under hypoxic compared to physioxic conditions, whereas the 8-oxo-Pu levels show an opposite trend, (iv) the diastereoisomeric ratios 5′R/5′S are independent of oxygen concentration being 0.29 for cdG and 2.69 for cdA for EUE-pBD650 (wt) and 0.32 for cdG and 2.94 for cdA for EUE-siXPA (deficient), (v) in deficient cell lines Fe levels were significantly higher. The data show for the first time the connection of oxygen concentration in cells with different DNA repair ability and the levels of different DNA lesions highlighting the significance of cPu. Membrane lipidomic data at 21% O(2) indicated differences in the fatty acid contents between wild type and deficient cells, envisaging functional effects on membranes associated with the different repair capabilities, to be further investigated. MDPI 2019-11-01 /pmc/articles/PMC6912421/ /pubmed/31683970 http://dx.doi.org/10.3390/cells8111377 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Krokidis, Marios G.
Parlanti, Eleonora
D’Errico, Mariarosaria
Pascucci, Barbara
Pino, Anna
Alimonti, Alessandro
Pietraforte, Donatella
Masi, Annalisa
Ferreri, Carla
Chatgilialoglu, Chryssostomos
Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title_full Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title_fullStr Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title_full_unstemmed Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title_short Purine DNA Lesions at Different Oxygen Concentration in DNA Repair-Impaired Human Cells (EUE-siXPA)
title_sort purine dna lesions at different oxygen concentration in dna repair-impaired human cells (eue-sixpa)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912421/
https://www.ncbi.nlm.nih.gov/pubmed/31683970
http://dx.doi.org/10.3390/cells8111377
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