Oxidative damage and impairment of protein quality control systems in keratinocytes exposed to a volatile organic compounds cocktail.
Marlène DezestMickael Le BechecLaurent ChavatteValérie DesauziersBenoît ChaputJean-Louis GrolleauPascal DescarguesCarine NizardSylvianne SchnebertSylvie LacombeAnne-Laure BulteauPublished in: Scientific reports (2017)
Compelling evidence suggests that volatile organic compounds (VOCs) have potentially harmful effects to the skin. However, knowledge about cellular signaling events and toxicity subsequent to VOC exposure to human skin cells is still poorly documented. The aim of this study was to focus on the interaction between 5 different VOCs (hexane, toluene, acetaldehyde, formaldehyde and acetone) at doses mimicking chronic low level environmental exposure and the effect on human keratinocytes to get better insight into VOC-cell interactions. We provide evidence that the proteasome, a major intracellular proteolytic system which is involved in a broad array of processes such as cell cycle, apoptosis, transcription, DNA repair, protein quality control and antigen presentation, is a VOC target. Proteasome inactivation after VOC exposure is accompanied by apoptosis, DNA damage and protein oxidation. Lon protease, which degrades oxidized, dysfunctional, and misfolded proteins in the mitochondria is also a VOC target. Using human skin explants we found that VOCs prevent cell proliferation and also inhibit proteasome activity in vivo. Taken together, our findings provide insight into potential mechanisms of VOC-induced proteasome inactivation and the cellular consequences of these events.
Keyphrases
- quality control
- cell cycle
- dna repair
- dna damage
- cell proliferation
- oxidative stress
- cell cycle arrest
- cell death
- induced apoptosis
- endoplasmic reticulum stress
- protein protein
- pi k akt
- healthcare
- endothelial cells
- diabetic rats
- amino acid
- wound healing
- single cell
- binding protein
- human health
- drug induced
- reactive oxygen species
- high glucose
- signaling pathway
- small molecule
- room temperature
- mass spectrometry
- induced pluripotent stem cells
- soft tissue