Environmental fluoxetine promotes skin cell proliferation and wound healing

被引:1
|
作者
Rodriguez-Barucg, Quentin [1 ]
Garcia, Angel A. [1 ]
Garcia-Merino, Belen [1 ,2 ]
Akinmola, Tomilayo [1 ]
Okotie-Eboh, Temisanren [1 ]
Francis, Thomas [1 ]
Bringas, Eugenio [2 ]
Ortiz, Inmaculada [2 ]
Wade, Mark A. [1 ]
Dowle, Adam [3 ]
Joyce, Domino A. [4 ]
Hardman, Matthew J. [1 ]
Wilkinson, Holly N. [1 ]
Beltran-Alvarez, Pedro [1 ]
机构
[1] Univ Hull, Biomed Inst Multimorbid, Ctr Biomed, Hull York Med Sch, Cottingham Rd, Kingston Upon Hull HU6 7RX, England
[2] Univ Cantabria, ETSIIT, Dept Chem & Biomol Engn, Castros S-N, Santander 39005, Spain
[3] Univ York, Metabol & Prote Lab, Biosci Technol Facil, Dept Biol, York YO10 5DD, England
[4] Univ Hull, Sch Nat Sci, Evolutionary & Ecol Genom Grp, Cottingham Rd, Kingston Upon Hull HU6 7RX, England
基金
英国工程与自然科学研究理事会;
关键词
Fluoxetine; Keratinocyte; Serotonin; Skin; Wound healing; SEROTONIN REUPTAKE INHIBITORS; PERSONAL CARE PRODUCTS; ANTIDEPRESSANT FLUOXETINE; THERAPEUTIC CLASSES; PREDATOR AVOIDANCE; WASTE-WATER; PHARMACEUTICALS; RECEPTOR; BEHAVIOR; IMPACT;
D O I
10.1016/j.envpol.2024.124952
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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.
引用
收藏
页数:14
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