PubMed · 2013 · 29 citations · 25 references
Life SciencesCell BiologyDermatologyApoptosisCell DivisionCellular PharmacologyApoptosis RegulationBcl-2 Family ProteinsCell DeathCell-cycle DysregulationCytotoxicity AssessmentBcl-2 Protein ExpressionCell Cycle Arrest MechanismsCell Cycle Arrest SignalingKeratinocyte BiologyMitochondrial Pathway Of Apoptosis
Citric acid is an alpha-hydroxyacid (AHA) widely used in cosmetic dermatology and skincare products. However, there is concern regarding its safety for the skin. In this study, we investigated the cytotoxic effects of citric acid on the human keratinocyte cell line HaCaT. HaCaT cells were treated with citric acid at 2.5-12.5 mM for different time periods. Cell-cycle arrest and apoptosis were investigated by 4,6-diamidino-2-phenylindole dihydrochloride (DAPI) staining, flow cytometry, western blot and confocal microscopy. Citric acid not only inhibited proliferation of HaCaT cells in a dose-dependent manner, but also induced apoptosis and cell cycle-arrest at the G2/M phase (before 24 h) and S phase (after 24 h). Citric acid increased the level of Bcl-2-associated X protein (BAX) and reduced the levels of B-cell lymphoma-2 (BCL-2), B-cell lymphoma-extra large (BCL-XL) and activated caspase-9 and caspase-3, which subsequently induced apoptosis via caspase-dependent and caspase-independent pathways. Citric acid also activated death receptors and increased the levels of caspase-8, activated BH3 interacting-domain death agonist (BID) protein, Apoptosis-inducing factor (AIF), and Endonuclease G (EndoG). Therefore, citric acid induces apoptosis through the mitochondrial pathway in the human keratinocyte cell line HaCaT. The study results suggest that citric acid is cytotoxic to HaCaT cells via induction of apoptosis and cell-cycle arrest in vitro.
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Su‐Hua Huang, Liu-Wei Wu, An-Cheng Huang et al. · Journal of Agricultural and Food Chemistry · 2011 · 111 citations
Medicine, Cell Biology, Pharmacology +16