Subject(s)
Interferon-alpha , Keratinocytes , Lupus Erythematosus, Cutaneous , Poly I-C , Humans , Keratinocytes/drug effects , Lupus Erythematosus, Cutaneous/drug therapy , Lupus Erythematosus, Cutaneous/pathology , Poly I-C/pharmacology , Poly I-C/administration & dosage , TYK2 Kinase/antagonists & inhibitors , TYK2 Kinase/metabolism , Protein Kinase Inhibitors/pharmacologyABSTRACT
Chloracne is the major skin symptom caused by dioxin intoxication. Dioxin activates the aryl hydrocarbon receptor (AHR)â»cytochrome p450 1A1 (CYP1A1) system, generates oxidative stress, and induces hyperkeratinization of keratinocytes and sebocytes leading to chloracne. Nuclear factor-erythroid 2-related factor-2 (NRF2) is a master switch that induces the expression of various antioxidative enzymes, such as heme oxygenase-1. Cinnamaldehyde is an antioxidant phytochemical that inhibits AHRâ»CYP1A1 signaling and activates the NRF2â»antioxidative axis. The cinnamaldehyde-containing Kampo herbal medicine Keishibukuryogan is capable of improving chloracne in Yusho patients who are highly contaminated with dioxin. Agents with dual functions in promoting AHRâ»CYP1A1 inhibition and NRF2 activation may be useful for managing dioxin-related health hazards.
ABSTRACT
[This corrects the article DOI: 10.1155/2018/9524657.].
ABSTRACT
The skin covers the outer surface of the body, so the epidermal keratinocytes within it are susceptible to reactive oxygen species (ROS) generated by environmental pollutants such as benzo(a)pyrene (BaP), a potent activator of aryl hydrocarbon receptor (AHR). Antioxidant activity is generally mediated by the nuclear factor-erythroid 2-related factor-2 (NRF2) and heme oxygenase-1 (HO1) axis in human keratinocytes. Perillaldehyde is the main component of Perilla frutescens, which is a medicinal antioxidant herb traditionally consumed in East Asia. However, the effect of perillaldehyde on the AHR/ROS and/or NRF2/HO1 pathways remains unknown. In human keratinocytes, we found that perillaldehyde (1) inhibited BaP-induced AHR activation and ROS production, (2) inhibited BaP/AHR-mediated release of the CCL2 chemokine, and (3) activated the NRF2/HO1 antioxidant pathway. Perillaldehyde is thus potentially useful for managing inflammatory skin diseases or disorders related to oxidative stress.
Subject(s)
Basic Helix-Loop-Helix Transcription Factors/antagonists & inhibitors , Keratinocytes/drug effects , Monoterpenes/pharmacology , NF-E2-Related Factor 2/metabolism , Receptors, Aryl Hydrocarbon/antagonists & inhibitors , Antioxidants/metabolism , Basic Helix-Loop-Helix Transcription Factors/metabolism , Benzo(a)pyrene/pharmacology , Cell Line , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Cell Survival/drug effects , Chemokine CCL2/biosynthesis , Cytochrome P-450 CYP1A1/antagonists & inhibitors , Cytochrome P-450 CYP1A1/biosynthesis , Heme Oxygenase-1/antagonists & inhibitors , Heme Oxygenase-1/metabolism , Humans , Keratinocytes/cytology , Keratinocytes/metabolism , Reactive Oxygen Species/antagonists & inhibitors , Reactive Oxygen Species/metabolism , Receptors, Aryl Hydrocarbon/metabolism , Signal Transduction/drug effectsABSTRACT
Wound healing is an elaborate process composed of overlapping phases, such as proliferation and remodeling, and is delayed in several circumstances, including diabetes. Although several treatment strategies for chronic wounds, such as growth factors, have been applied, further alternatives are required. The skin, especially keratinocytes, is continually exposed to UV rays, which impairs wound healing. 6-Formylindolo[3,2-b]carbazole (FICZ) is a tryptophan photoproduct formed by UV exposure, indicating that FICZ might be one of the effectors of UV radiation. In contrast, treatment with tryptophan, the precursor for FICZ, promoted wound closure in keratinocytes. Therefore, the aim of our study was to determine the role of FICZ in wound healing. Here we showed that FICZ enhanced keratinocyte migration through mitogen-activated protein kinase/extracellular signal-regulated kinase activation, and promoted wound healing in various mouse models, including db/db mice, which exhibit wound healing impairments because of type 2 diabetes. Moreover, FICZ, the endogenous ligand of an aryl hydrocarbon receptor, accelerated migration even in the aryl hydrocarbon receptor knockdown condition and also promoted wound healing in DBA/2 mice, bearing a low-affinity aryl hydrocarbon receptor, suggesting that FICZ enhanced keratinocyte migration in a mitogen-activated protein kinase/extracellular signal-regulated kinase-dependent, but aryl hydrocarbon receptor-independent, manner. The function of FICZ might indicate the possibility of its clinical use for intractable chronic wounds.
Subject(s)
Carbazoles/pharmacology , Diabetes Mellitus, Experimental , Extracellular Signal-Regulated MAP Kinases/metabolism , Receptors, Aryl Hydrocarbon/metabolism , Skin/pathology , Wound Healing/drug effects , Animals , Cell Line , Cell Movement , Humans , Keratinocytes/metabolism , Mice , Mice, Inbred DBA , Skin/drug effects , Skin/metabolismSubject(s)
Collagen Type VII/genetics , Epidermolysis Bullosa Dystrophica/complications , Genetic Predisposition to Disease , Skin Diseases/etiology , Xanthomatosis/etiology , Biopsy, Needle , Disease Progression , Epidermolysis Bullosa Dystrophica/genetics , Epidermolysis Bullosa Dystrophica/pathology , Female , Humans , Immunohistochemistry , Mutation , Prognosis , Rare Diseases , Risk Assessment , Skin Diseases/physiopathology , Xanthomatosis/physiopathology , Young AdultABSTRACT
S100P is a member of the S100 family. Increased levels of S100P have been documented in various malignancies. Binding of extracellular S100P to receptor for advanced glycation end products (RAGE) or coupling of intracellular S100P with a cytoskeletal protein, ezrin, play a crucial role in tumor growth, invasion and metastasis. However, little is known about the expression of S100P, RAGE and ezrin in malignant melanoma. We immunostained these three molecules in 20 primary and 20 metastatic melanomas. Samples of 20 benign nevus pigmentosus and 10 of normal skin were tested as controls. The expression levels (percentage of positively stained cells) of S100P, RAGE and ezrin were significantly higher in melanomas than in nevus pigmentosus. Moreover, slightly but significantly higher expression levels were observed in metastatic than in primary melanomas. Significant positive correlations were evident between the expression levels of S100P and RAGE, S100P and ezrin, and RAGE and ezrin, respectively. In conclusion, the coordinate upregulation of S100P, RAGE and ezrin may possibly facilitate malignant transformation of melanoma.
