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Environmental fluoxetine promotes skin cell proliferation and wound healing

Rodriguez-Barucg, Quentin; Garcia, Angel A.; Garcia-Merino, Belen; Akinmola, Tomilayo; Okotie-Eboh, Temisanren; Francis, Thomas; Bringas, Eugenio; Ortiz, Inmaculada; Wade, Mark; Dowle, Adam; Joyce, Domino A.; Hardman, Matthew J.; Wilkinson, Holly N.; Beltran-Alvarez, Pedro

Authors

Quentin Rodriguez-Barucg

Angel A. Garcia

Belen Garcia-Merino

Tomilayo Akinmola

Temisanren Okotie-Eboh

Thomas Francis

Eugenio Bringas

Inmaculada Ortiz

Profile image of Mark Wade

Dr Mark Wade M.Wade@hull.ac.uk
Senior Lecturer in Molecular Genetics

Adam Dowle

Profile image of Pedro Beltran-Alvarez

Dr Pedro Beltran-Alvarez P.Beltran-Alvarez@hull.ac.uk
Senior Lecturer in Health and Climate Change and Programme co-Director of the MSc Health and Climate Change



Abstract

This study investigates the effects of environmentally-relevant concentrations of fluoxetine (FLX, commercial name: Prozac) on wound healing. Pollution of water systems with pharmaceutical and personal care products, including antidepressants such as FLX and other selective serotonin reuptake inhibitors, is a growing environmental concern. Environmentally-relevant FLX concentrations are known to impact physiological functions and behaviour of aquatic animals, however, the effects of exposure on humans are currently unknown. Using a combination of human skin biopsies and a human keratinocyte cell line, we show that exposure to environmental FLX promotes wound closure. We show dose-dependent increases in wound closure with FLX concentrations from 125 ng/l. Using several –omics and pharmaceutical approaches, we demonstrate that the mechanisms underlying enhanced wound closure are increased cell proliferation and serotonin signalling. Transcriptomic analysis revealed 350 differentially expressed genes after exposure. Downregulated genes were enriched in pathways related to mitochondrial function and metabolism, while upregulated genes were associated with cell proliferation and tissue morphogenesis. Kinase profiling showed altered phosphorylation of kinases linked to the MAPK pathway. Consistent with this, phosphoproteomic analyses identified 235 differentially phosphorylated proteins after exposure, with enriched GO terms related to cell cycle, division, and protein biosynthesis. Treatment of skin biopsies and keratinocytes with ketanserin, a serotonin receptor antagonist, reversed the increase in wound closure observed upon exposure. These findings collectively show that exposure to environmental FLX promotes wound healing through modulating serotonin signalling, gene expression and protein phosphorylation, leading to enhanced cell proliferation. Our results justify a transition from the study of behavioural effects of environmental FLX in aquatic animals to the investigation of effects of exposure on wound healing in aquatic and terrestrial animals, including direct impacts on human health.

Citation

Rodriguez-Barucg, Q., Garcia, A. A., Garcia-Merino, B., Akinmola, T., Okotie-Eboh, T., Francis, T., Bringas, E., Ortiz, I., Wade, M., Dowle, A., Joyce, D. A., Hardman, M. J., Wilkinson, H. N., & Beltran-Alvarez, P. (2024). Environmental fluoxetine promotes skin cell proliferation and wound healing. Environmental pollution, 362, Article 124952. https://doi.org/10.1016/j.envpol.2024.124952

Journal Article Type Article
Acceptance Date Sep 12, 2024
Online Publication Date Sep 14, 2024
Publication Date Dec 1, 2024
Deposit Date Sep 12, 2024
Publicly Available Date Sep 20, 2024
Journal Environmental Pollution
Print ISSN 0269-7491
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 362
Article Number 124952
DOI https://doi.org/10.1016/j.envpol.2024.124952
Public URL https://hull-repository.worktribe.com/output/4830113

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