دورية أكاديمية

Melanopsin (OPN4) is a novel player in skin homeostasis and attenuates UVA-induced effects.

التفاصيل البيبلوغرافية
العنوان: Melanopsin (OPN4) is a novel player in skin homeostasis and attenuates UVA-induced effects.
المؤلفون: Sua-Cespedes C; Department of Physiology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil., Lacerda JT; Department of Physiology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil., Zanetti G; Department of Physiology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil., David DD; Department of Physiology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil., Moraes MN; Department of Biological Sciences, Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of São Paulo, São Paulo, Brazil., de Assis LVM; Institute of Neurobiology, University of Lübeck, Lübeck, Germany., Castrucci AML; Department of Physiology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil; Department of Biology, University of Virginia, Charlottesville, USA. Electronic address: amdlcast@ib.usp.br.
المصدر: Journal of photochemistry and photobiology. B, Biology [J Photochem Photobiol B] 2023 May; Vol. 242, pp. 112702. Date of Electronic Publication: 2023 Mar 28.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Elsevier Sequoia Country of Publication: Switzerland NLM ID: 8804966 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2682 (Electronic) Linking ISSN: 10111344 NLM ISO Abbreviation: J Photochem Photobiol B Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Lausanne : Elsevier Sequoia, 1987-
مواضيع طبية MeSH: Rod Opsins*/genetics , Rod Opsins*/metabolism , Skin*/metabolism, Animals ; Mice ; Homeostasis ; Melanocytes/metabolism ; Membrane Proteins/metabolism ; Ultraviolet Rays/adverse effects
مستخلص: The presence of melanopsin (OPN4) has been shown in cultured murine melanocytes and was associated with ultraviolet A radiation (UVA) reception. Here we demonstrated the protective role of OPN4 in skin physiology and the increased UVA-induced damage in its absence. Histological analysis showed a thicker dermis and thinner hypodermal white adipose tissue layer in Opn4 -/- (KO) mice than in wild-type (WT) animals. Proteomics analyses revealed molecular signatures associated with proteolysis, remodeling chromatin, DNA damage response (DDR), immune response, and oxidative stress coupled with antioxidant responses in the skin of Opn4 KO mice compared to WT. Skin protein variants were found in Opn4 KO mice and Opn2, Opn3, and Opn5 gene expressions were increased in the genotype. We investigated each genotype response to UVA stimulus (100 kJ/m 2 ). We found an increase of Opn4 gene expression following stimulus on the skin of WT mice suggesting melanopsin as a UVA sensor. Proteomics findings suggest that UVA decreases DDR pathways associated with ROS accumulation and lipid peroxidation in the skin of Opn4 KO mice. Relative changes in methylation (H3-K79) and acetylation sites of histone between genotypes and differentially modulated by UVA stimulus were also observed. We also identified alterations of molecular traits of the central hypothalamus-pituitary- adrenal (HPA) and the skin HPA-like axes in the absence of OPN4. Higher skin corticosterone levels were detected in UVA-stimulated Opn4 KO compared to irradiated WT mice. Taken altogether, functional proteomics associated with gene expression experiments allowed a high-throughput evaluation that suggests an important protective role of OPN4 in regulating skin physiology in the presence and absence of UVA radiation.
Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2023 Elsevier B.V. All rights reserved.)
فهرسة مساهمة: Keywords: Melanopsin; Neuroendocrine axes; Proteomics; Skin; UVA radiation
المشرفين على المادة: 0 (melanopsin)
0 (Membrane Proteins)
0 (OPN3 protein, mouse)
0 (OPN5 protein, mouse)
0 (Rod Opsins)
تواريخ الأحداث: Date Created: 20230405 Date Completed: 20230411 Latest Revision: 20230411
رمز التحديث: 20240628
DOI: 10.1016/j.jphotobiol.2023.112702
PMID: 37018912
قاعدة البيانات: MEDLINE
الوصف
تدمد:1873-2682
DOI:10.1016/j.jphotobiol.2023.112702