Energy metabolism rewiring following acute UVB irradiation is largely dependent on nuclear DNA damage

Léa Dousset, Walid Mahfouf, Hadi Younes, Hala Fatrouni, Corinne Faucheux, Elodie Muzotte, Ferial Khalife, Rodrigue Rossignol, François Moisan, Muriel Cario, Stéphane Claverol, Laure Favot-Laforge, Anni I. Nieminen, Seppo Vainio, Nsrein Ali, Hamid Reza Rezvani

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Solar ultraviolet B (UVB) radiation-induced DNA damage is a well-known initiator of skin carcinomas. The UVB-induced DNA damage response (DDR) involves series of signaling cascades that are activated to maintain cell integrity. Among the different biological processes, little is known about the role of energy metabolism in the DDR. We sought to determine whether UVB-induced nuclear and/or mitochondrial cyclobutane pyrimidine dimers (CPDs) alter cellular energy metabolism. To gain insight into this question, we took advantage of keratinocytes expressing nuclear or mitochondrial CPD photolyase. Applying a quantitative proteomic approach and targeted metabolomics, we observed biphasic alterations in multiple metabolic pathways and in the abundance of various metabolites, largely influenced by the presence of genomic CPDs. The heightened oxygen consumption rate post-irradiation, along with mitochondrial structural rearrangements, was found to be dependent on both mitochondrial and nuclear CPDs. Understanding the influence of nuclear and mitochondrial DNA damage on keratinocyte responses to UVB irradiation deepens current knowledge regarding skin cancer prevention, initiation, and therapy.

Original languageEnglish
JournalFree Radical Biology and Medicine
Volume227
Pages (from-to)459-471
Number of pages13
ISSN0891-5849
DOIs
Publication statusPublished - 1 Feb 2025
MoE publication typeA1 Journal article-refereed

Bibliographical note

Publisher Copyright:
© 2024 The Authors

Fields of Science

  • 1182 Biochemistry, cell and molecular biology
  • Hypoxia-inducible factor-1-alpha
  • Induced apoptosis
  • Mitochondrial
  • Cells
  • Expression
  • Repair
  • Inhibition
  • Activation
  • Stress
  • Growth

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