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Melanin Photosensitization and the Effect of Visible Light on Epithelial Cells
Author(s) -
Orlando Chiarelli-Neto,
Alan S. Ferreira,
Waleska K. Martins,
Christiane Pavani,
Divinomar Severino,
Fernanda FaiãoFlores,
Silvya Stuchi MariaEngler,
Eduardo Aliprandini,
Gláucia Regina Martinez,
Paolo Di Mascio,
Marisa Helena Gennari de Medeiros,
Maurı́cio S. Baptista
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0113266
Subject(s) - melanin , photobleaching , photoaging , dna damage , singlet oxygen , visible spectrum , photoprotection , chemistry , human skin , photobiology , cell damage , biophysics , microbiology and biotechnology , biology , dna , fluorescence , biochemistry , oxygen , materials science , genetics , optoelectronics , optics , physics , photosynthesis , organic chemistry , botany
Protecting human skin from sun exposure is a complex issue that involves unclear aspects of the interaction between light and tissue. A persistent misconception is that visible light is safe for the skin, although several lines of evidence suggest otherwise. Here, we show that visible light can damage melanocytes through melanin photosensitization and singlet oxygen ( 1 O 2 ) generation, thus decreasing cell viability, increasing membrane permeability, and causing both DNA photo-oxidation and necro-apoptotic cell death. UVA (355 nm) and visible (532 nm) light photosensitize 1 O 2 with similar yields, and pheomelanin is more efficient than eumelanin at generating 1 O 2 and resisting photobleaching. Although melanin can protect against the cellular damage induced by UVB, exposure to visible light leads to pre-mutagenic DNA lesions (i.e., Fpg- and Endo III-sensitive modifications); these DNA lesions may be mutagenic and may cause photoaging, as well as other health problems, such as skin cancer.

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