How does the skin sense sun light? An integrative view of light sensing molecules
Tài liệu tham khảo
Leiter, 2014, Epidemiology of skin cancer, Adv. Exp. Med. Biol., 810, 120
Cohen, 2020, Cutaneous interaction with visible light: what do we know, J. Am. Acad. Dermatol., 10.1016/j.jaad.2020.03.115
AAD (American Academy of Dermatology), Vitamin D and UV exposure, (n.d.). https://www.aad.org/media/stats/prevention-and-care/vitamin-d-and-uv-exposure.
Apalla, 2017, Epidemiological trends in skin cancer, Dermatol. Pract. Concept., 7, 1, 10.5826/dpc.0702a01
TMR (Transparency Market Research), 2015
Kolbe, 2012, How much sun protection is needed?: Are we on the way to full-spectrum protection?, J. Invest. Dermatol., 132, 1756, 10.1038/jid.2012.148
Liebel, 2012, Irradiation of skin with visible light induces reactive oxygen species and matrix-degrading enzymes, J. Invest. Dermatol., 132, 1901, 10.1038/jid.2011.476
Tonolli, 2017, Lipofuscin generated by UVA turns keratinocytes photosensitive to visible light, J. Invest. Dermatol., 137, 2447, 10.1016/j.jid.2017.06.018
Markiewicz, 2020, Melanogenic difference consideration in ethic skin type: a balance approach between skin brightening applications and beneficial sun exposure, Clin. Cosm. Investig. Dermatol., 13, 215, 10.2147/CCID.S245043
Brenner, 2008, The protective role of melanin against UV damage in human skin, Photochem. Photobiol., 84, 539, 10.1111/j.1751-1097.2007.00226.x
Zastrow, 2009, The missing link - Light-induced (280-1,600 nm) free radical formation in human skin, Skin Pharmacol. Physiol., 22, 31, 10.1159/000188083
Cho, 2009, Effects of infrared radiation and heat on human skin aging in vivo, J. Investig. Dermatol. Symp. Proc., 14, 15, 10.1038/jidsymp.2009.7
George, 2018, Effect of red light and near infrared laser on the generation of reactive oxygen species in primary dermal fibroblasts, J. Photochem. Photobiol. B, Biol., 188, 60, 10.1016/j.jphotobiol.2018.09.004
Regazzetti, 2017, Melanocytes sense blue light and regulate pigmentation through opsin-3, J. Invest. Dermatol., 138, 171, 10.1016/j.jid.2017.07.833
de Assis, 2018, Melanopsin and rhodopsin mediate UVA-induced immediate pigment darkening:unravelling the photosensitive system of the skin, Eur. J. Cell Biol., 97, 150, 10.1016/j.ejcb.2018.01.004
Kaidbey, 1979, Photoprotection by melanin—a comparison of black and Caucasian skin, J. Am. Acad. Dermatol., 1, 249, 10.1016/S0190-9622(79)70018-1
Chiarelli-Neto, 2011, Generation and suppression of singlet oxygen in hair by photosensitization of melanin, Free Rad. Biol. Med., 51, 1195, 10.1016/j.freeradbiomed.2011.06.013
Chiarelli-Neto, 2014, Photosensitization of melanin and the effect of visible light on skin and hair, PLoS One, 9, e113266, 10.1371/journal.pone.0113266
Chiarelli-Neto, 2016, Photosensitizing properties of melanin upon excitation with visible light, Trends Photochem. Photobiol., 17, 57
Vashi, 2016, Aging differences in ethnic skin, J. Clin. Aesthet. Dermatol., 9, 31
Davis, 2011, Vitamin D deficiency and type 2 diabetes in African Americans: the common denominators, Diabetes Spectr., 24, 148, 10.2337/diaspect.24.3.148
1992, IARC 1992 IARC Monograph on the evaluation of carcinogenic risks to human. Solar and ultraviolet radiation, IARC Monogr. Eval. Carcinog. Risks Hum., 55, 1
Matsui, 2009, Non- sunscreen photoprotection: antioxidants add value to a sunscreen, JID Symp. Proc., 14, 56
Eberlein-König, 2005, Relevance of vitamins C and E in cutaneous photoprotection, J. Cosmet. Dermatol., 4, 4, 10.1111/j.1473-2165.2005.00151.x
Freitas, 2019, Antioxidant role on the protection of melanocytes against visible light-induced photodamage, Free Rad. Biol. Med., 131, 399, 10.1016/j.freeradbiomed.2018.12.028
IARC, 2001, IARC handbooks of cancer prevention, Volume 5
Dennis, 2003, Sunscreen use and the risk for melanoma: a quantitative review, Ann. Intern. Med., 139, 966, 10.7326/0003-4819-139-12-200312160-00006
Gallagher, 2005, Sunscreens in melanoma and skin cancer prevention, CMAJ, 173, 244, 10.1503/cmaj.050762
DiNardo, 2018, Dermatological and environmental toxicological impact of the sunscreen ingredient oxybenzone/benzophenone-3, J. Cosmet. Dermatol., 17, 15, 10.1111/jocd.12449
2019, FDA proposes changes to US sunscreen rules
Downs, 2016, Toxicopathological effects of the sunscreen UV filter, oxybenzone (benzophenone-3), on coral planulae and cultured primary cells and its environmental contamination in Hawaii and the U.S. Virgin Islands, Arch. Environ. Contam. Toxicol., 70, 265, 10.1007/s00244-015-0227-7
Danovaro, 2008, Sunscreens cause coral bleaching by promoting viral infections, Environ. Health Perspect., 116, 421, 10.1289/ehp.10966
2018
Naeem, 2010, Vitamin d deficiency- an ignored epidemic, Int. J. Health Sci. (Qassim), 4, V
Pilz, 2016, Vitamin D and cardiovascular disease prevention, Nat. Rev. Cardiol., 13, 404, 10.1038/nrcardio.2016.73
Civitelli, 2011, Calcium and phosphate homeostasis: concerted interplay of new regulators, J. Endocrinol. Invest., 34, 3
Aranow, 2012, Vitamin D and the immune system, J. Investig. Med., 59, 881, 10.2310/JIM.0b013e31821b8755
Penckofer, 2010, Vitamin D and depression: where is all the sunshine, Issues Ment. Health Nurs., 31, 385, 10.3109/01612840903437657
Samanek, 2006, Estimates of beneficial and harmful sun exposure times during the year for major Australian population centres, Med. J. Aust., 184, 338, 10.5694/j.1326-5377.2006.tb00267.x
Holick, 2008, Vitamin D deficiency: a worldwide problem with health consequences, Am. J. Clin. Nutr., 87, 1080S, 10.1093/ajcn/87.4.1080S
Grant, 2007, An estimate of cancer mortality rate reductions in Europe and the US with 1,000 IU of oral vitamin D per day, Recent Results Cancer Res., 174, 225, 10.1007/978-3-540-37696-5_20
CDC, 2014
Haltaufderhyde, 2015, Opsin expression in human epidermal skin, Photochem. Photobiol., 91, 117, 10.1111/php.12354
Ozdeslik, 2019, Human nonvisual opsin 3 regulates pigmentation of epidermal melanocytes through functional interaction with melanocortin 1 receptor, Proc. Natl. Acad. Sci. U. S. A., 116, 11508, 10.1073/pnas.1902825116
Leung, 2017, Unconventional roles of opsins, Annu. Rev. Cell Dev. Biol., 33, 241, 10.1146/annurev-cellbio-100616-060432
Duffy, 2009, Effect of light on human circadian physiology, Sleep Med. Clin., 4, 165, 10.1016/j.jsmc.2009.01.004
Roenneberg, 2013, Light and the human circadian clock, Handb. Exp. Pharmacol., 217, 311, 10.1007/978-3-642-25950-0_13
Roenneberg, 2016, The circadian clock and human health, Curr. Biol., 26, R432, 10.1016/j.cub.2016.04.011
Fleury, 2016, Sun exposure and its effects on human health: mechanisms through which sun exposure could reduce the risk of developing obesity and cardiometabolic dysfunction, Int. J. Environ. Res. Public Health, 13, 999, 10.3390/ijerph13100999
Liu, 2014, UVA irradiation of human skin vasodilates arterial vasculature and lowers blood pressure independently of nitric oxide synthase, J. Invest. Dermatol., 134, 1839, 10.1038/jid.2014.27
Halliday, 2014, An unexpected role: UVA-induced release of nitric oxide from skin may have unexpected health benefits, J. Invest. Dermatol., 134, 1791, 10.1038/jid.2014.33
Weller, 2016, Sunlight has cardiovascular benefits independently of vitamin D, Blood Purif., 41, 130, 10.1159/000441266
Ondrusova, 2017, Subcutaneous white adipocytes express a light sensitive signaling pathway mediated via a melanopsin/TRPC channel axis, Sci. Rep., 7, 16332, 10.1038/s41598-017-16689-4
Lindqvist, 2016, Avoidance of sun exposure as a risk factor for major causes of death: a competing risk analysis of the melanoma in Southern Sweden cohort, J. Intern. Med., 280, 375, 10.1111/joim.12496
McLafferty, 2012, The integumentary system: anatomy, physiology and function of skin, Nurs. Stand., 27, 35, 10.7748/ns2012.09.27.3.35.c9299
Slominski, 2004, Melanin pigmentation in mammalian skin and its hormonal regulation, Physiol. Rev., 84, 1155, 10.1152/physrev.00044.2003
Lin, 2007, Melanocyte biology and skin pigmentation, Nature, 445, 843, 10.1038/nature05660
Sklar, 2013, Effects of ultraviolet radiation, visible light, and infrared radiation on erythema and pigmentation: a review, Photochem. Photobiol. Sci., 12, 54, 10.1039/c2pp25152c
Rivera-Gonzalez, 2014, Adipocytes in skin health and disease, Cold Spring Harb. Perspect. Med., 4, 10.1101/cshperspect.a015271
Kruglikov, 2016, Dermal adipocytes: from irrelevance to metabolic targets?, Trends Endocrinol. Metab., 27, 1, 10.1016/j.tem.2015.11.002
Passeron, 2020, Clinical and biological impact of the exposome on the skin, J. Eur. Acad. Dermatol. Venereol., 34, 4, 10.1111/jdv.16614
Dupont, 2013, Beyond UV radiation: a skin under challenge, Int. J. Cosmet. Sci., 35, 224, 10.1111/ics.12036
Mahmoud, 2008, Effects of visible light on the skin, Photochem. Photobiol., 84, 450, 10.1111/j.1751-1097.2007.00286.x
D’Orazio, 2013, UV radiation and the skin, Int. J. Mol. Sci., 14, 12222, 10.3390/ijms140612222
Clement, 2005, Optimising the design of a broad-band light source for the treatment of skin, J. Cosmet. Laser Ther., 7, 177, 10.1080/14764170500344575
Ash, 2017, Effect of wavelength and beam width on penetration in light-tissue interaction using computational methods, Lasers Med. Sci., 32, 1909, 10.1007/s10103-017-2317-4
Ridley, 2009, Cellular and sub-cellular responses to UVA in relation to carcinogenesis, Int. J. Radiat. Biol., 85, 177, 10.1080/09553000902740150
Brand, 2018, Targeting mitochondrial oxidative stress to mitigate UV-induced skin damage, Front. Pharmacol., 9, 920, 10.3389/fphar.2018.00920
Mullenders, 2018, Solar UV damage to cellular DNA: from mechanisms to biological effects, Photochem. Photobiol. Sci., 17, 1842, 10.1039/c8pp00182k
Skobowiat, 2015, UVB activates hypothalamic-pituitary-adrenal axis in C57BL/6 mice, J. Invest. Dermatol., 135, 1638, 10.1038/jid.2014.450
Albers, 2019, Blue light (lambda=453nm) nitric oxide dependently induces beta-endorphin production of human skin keratinocytes in-vitro and increases systemic beta-endorphin levels in humans in-vivo, Free Radic. Biol. Med., 145, 78, 10.1016/j.freeradbiomed.2019.09.022
Holick, 2017, Ultraviolet B radiation: the vitamin d connection, Adv. Exp. Med. Biol., 996, 137, 10.1007/978-3-319-56017-5_12
Liebmann, 2010, Blue-light irradiation regulates proliferation and differentiation in human skin cells, J. Invest. Dermatol., 130, 259, 10.1038/jid.2009.194
Buscone, 2017, A new path in defining light parameters for hair growth: discovery and modulation of photoreceptors in human hair follicle, Lasers Surg. Med., 49, 705, 10.1002/lsm.22673
Kim, 2016, Short wavelength visible light suppresses innate immunity-related responses by modulating protein S-nitrosylation in keratinocytes, J. Invest. Dermatol., 136, 727, 10.1016/j.jid.2015.12.004
Oh, 2016, Blue light emitting diode induces apoptosis in lymphoid cells by stimulating autophagy, Int. J. Biochem. Cell Biol., 70, 13, 10.1016/j.biocel.2015.11.004
Sikka, 2014, Melanopsin mediates light-dependent relaxation in blood vessels, Proc. Natl. Acad. Sci. U. S. A., 111, 17977, 10.1073/pnas.1420258111
Kim, 2013, Violet light down- regulates the expression of specific differentiation markers through rhodopsin in normal human epidermal keratinocytes, PLoS One, 8, 10.1371/journal.pone.0073678
Catao, 2016, Green LED light has anti-inflammatory effects on burns in rats, Burns, 42, 392, 10.1016/j.burns.2015.07.003
Simoes, 2020, Photobiomodulation of red and green lights in the repair process of third-degree skin burns, Lasers Med. Sci., 35, 51, 10.1007/s10103-019-02776-7
Chen, 2018, Light-emitting diode 585nm photomodulation inhibiting melanin synthesis and inducing autophagy in human melanocytes, J. Dermatol. Sci., 89, 11, 10.1016/j.jdermsci.2017.10.001
Kim, 2017, A protective mechanism of visible red light in normal human dermal fibroblasts: enhancement of GADD45A-mediated DNA repair activity, J. Invest. Dermatol., 137, 466, 10.1016/j.jid.2016.07.041
Rohringer, 2017, The impact of wavelengths of LED light-therapy on endothelial cells, Sci. Rep., 7, 10700, 10.1038/s41598-017-11061-y
Ma, 2018, Effect of low-level laser therapy on proliferation and collagen synthesis of human fibroblasts in vitro, J. Wound Manag. Res., 14, 1, 10.22467/jwmr.2018.00283
Opel, 2015, Light- emitting diodes: a brief review and clinical experience, J. Clin. Aesthet. Dermatol., 8, 36
Serrage, 2019, Under the spotlight: mechanisms of photobiomodulation concentrating on blue and green light, Photochem. Photobiol. Sci., 18, 1877, 10.1039/c9pp00089e
Mignon, 2017, Photobiomodulation of human dermal fibroblasts in vitro: decisive role of cell culture conditions and treatment protocols on experimental outcome, Sci. Rep., 7, 2797, 10.1038/s41598-017-02802-0
Slominski, 2000, Neuroendocrinology of the skin, Endocr. Rev., 21, 457
Slominski, 2012, Sensing the environment: regulation of local and global homeostasis by the skin’s neuroendocrine system, Adv. Anat. Embryol. Cell Biol., 212, 1
Raj, 2006, Keratinocyte apoptosis in epidermal development and disease, J. Invest. Dermatol., 126, 243, 10.1038/sj.jid.5700008
Costanzo, 2015, Programmed cell death in the skin, Int. J. Dev. Biol., 59, 73, 10.1387/ijdb.150050ac
Mohania, 2017, Ultraviolet radiations: skin defense-damage mechanism, Adv. Exp. Med. Biol., 996, 71, 10.1007/978-3-319-56017-5_7
Dakup, 2017, Impact of the circadian clock on UV-induced DNA damage response and photocarcinogenesis, Photochem. Photobiol., 93, 296, 10.1111/php.12662
Rinnerthaler, 2015, Oxidative stress in aging human skin, Biomolecules, 5, 545, 10.3390/biom5020545
Polefka, 2016, Cutaneous oxidative stress and aging, 651
Wang, 2017, Time-restricted feeding shifts the skin circadian clock and alters UVB-induced DNA damage, Cell Rep., 20, 1061, 10.1016/j.celrep.2017.07.022
de Assis, 2019, The molecular clock in the skin, its functionality, and how it is disrupted in cutaneous melanoma: a new pharmacological target?, Cell. Mol. Life Sci., 76, 3801, 10.1007/s00018-019-03183-5
Welz, 2019, BMAL1-driven tissue clocks respond independently to light to maintain homeostasis, Cell, 177, 1436, 10.1016/j.cell.2019.05.009
Schlosser, 1991, Atmospheric effects on starlight and sunlight, 98
Bohm, 2002, Thermal effect of glazing in driver’s cabs: evaluation of the impact of different types of glazing on the thermal comfort, Semant. Sch.- Environ. Sci.
Hanafi, 2005, In vivo measurement of lower back deformations with Fourier-transform profilometry, Appl. Opt., 44, 2266, 10.1364/AO.44.002266
Anderson, 1981, The optics of human skin, J. Invest. Dermatol., 77, 13, 10.1111/1523-1747.ep12479191
Schroeder, 2010, Photoprotection beyond ultraviolet radiation – effective sun protection has to include protection against infrared A radiation-induced skin damage, Skin Pharmacol. Physiol., 23, 15, 10.1159/000257259
Scenihr, 2012
Barun, 2007, Absorption spectra and light penetration depth of normal and pathologically altered human skin, J. Appl. Spectrosc., 74, 430, 10.1007/s10812-007-0071-2
Henderson, 2004, 474
Leff, 1967, A mutagenic effect of visible light mediated by endogenous pigments in Euglena gracilis, Science, 158, 1332, 10.1126/science.158.3806.1332
Pfeifer, 2005, Mutations induced by ultraviolet light, Mutat. Res. Mol. Mech. Mutagen., 571, 19, 10.1016/j.mrfmmm.2004.06.057
Pfeifer, 2012, UV wavelength-dependent DNA damage and human non- melanoma and melanoma skin cancer, Photochem. Photobiol. Sci., 11, 90, 10.1039/c1pp05144j
Deaton, 2011, CpG islands and the regulation of transcription, Genes Dev., 25, 1010, 10.1101/gad.2037511
Cadet, 2005, Ultraviolet radiation-mediated damage to cellular DNA, Mutat. Res. – Fundam. Mol. Mech. Mutagen., 571, 3, 10.1016/j.mrfmmm.2004.09.012
Li, 2006, Similarities and differences between cyclobutane pyrimidine dimer photolyase and (6-4) photolyase as revealed by resonance Raman spectroscopy: electron transfer from the FAD cofactor to ultraviolet-damaged DNA, J. Biol. Chem., 281, 25551, 10.1074/jbc.M604483200
Tasso, 2019, Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers, J. Am. Chem. Soc., 141, 15547, 10.1021/jacs.9b05991
Baptista, 2017, Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways, Photochem. Photobiol., 93, 912, 10.1111/php.12716
Bacellar, 2018, Photosensitized membrane permeabilization requires contact- dependent reactions between photosensitizer and lipids, J. Am. Chem. Soc., 140, 9606, 10.1021/jacs.8b05014
Baier, 2006, Singlet oxygen generation by UVA light exposure of endogenous photosensitizers, Biophys. J., 91, 1452, 10.1529/biophysj.106.082388
Wondrak, 2006, Endogenous UVA-photosensitizers: mediators of skin photodamage and novel targets for skin photoprotection, Photochem. Photobiol. Sci., 5, 215, 10.1039/b504573h
Miyachi, 1995, Photoaging from an oxidative standpoint, J. Dermatol. Sci., 9, 79, 10.1016/0923-1811(94)00363-J
Gorman, 1987, Ergosterol (provitamin D2) triplet state: an efficient sensitizer of singlet oxygen, O2(Δg), formation, Photochem. Photobiol., 45, 215, 10.1111/j.1751-1097.1987.tb05366.x
Gorman, 1990, A pulse radiolysis and pulsed laser study of the vitamin D3 triplet state: lifetime, relaxation and nonvertical excitation, Photochem. Photobiol., 51, 29, 10.1111/j.1751-1097.1990.tb01680.x
Oliveros, 1995, Singlet oxygen (1Δg) sensitization and quenching by vitamin B12 derivatives, J. Photochem. Photobiol. B, Biol., 29, 37
Feis, 1997, Role of the triplet state in retinal photoisomerization as studied by laser-induced optoacoustic spectroscopy, J. Phys. Chem. B, 101, 7620, 10.1021/jp970879d
Bhattacharyya, 1985, Quantitative aspects of all-trans-retinol singlet and triplet quenching by oxygen, Chem. Phys. Lett., 116, 326, 10.1016/0009-2614(85)80178-0
Silva, 2015, Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites, Tetrahedron, 71, 457, 10.1016/j.tet.2014.11.072
Consiglieri, 2019, Single mutation in a novel bacterial LOV protein yields a singlet oxygen generator, Photochem. Photobiol. Sci., 18, 2657, 10.1039/c9pp00328b
Thomas, 2003, Singlet oxygen (1Δg) production by pterin derivatives in aqueous solutions, Photochem. Photobiol. Sci., 2, 245, 10.1039/b209993d
Bishop, 1994, Singlet oxygen sensitisation by excited state DNA, J. Chem. Soc. Chem. Commun., 1994, 871, 10.1039/c39940000871
Chin, 2008, Quantitative determination of singlet oxygen generated by excited state aromatic amino acids, proteins, and immunoglobulins, J. Am. Chem. Soc., 52, 7671
Egorov, 1991, Laser-induced luminescence of singlet molecular oxygen: generation by drugs and pigments of biological importance, Proc. SPIE 1403, Laser Appl. Life Sci.
Uchoa, 2008, Singlet oxygen generation in the reaction centers of Rhodobacter sphaeroides, Eur. Biophys. J., 37, 843, 10.1007/s00249-008-0287-y
Rózanowska, 1998, Blue light-induced singlet oxygen generation by retinal lipofuscin in non-polar media, Free Radic. Biol. Med., 24, 1107, 10.1016/S0891-5849(97)00395-X
Spudich, 2000, Retinylidene proteins: structures and functions from archaea to humans, Annu. Rev. Cell Dev. Biol., 16, 365, 10.1146/annurev.cellbio.16.1.365
Kefalov, 2012, Rod and cone visual pigments and phototransduction through pharmacological, genetic, and physiological approaches, J. Biol. Chem., 287, 1635, 10.1074/jbc.R111.303008
Terakita, 2014, Functional properties of opsins and their contribution to light- sensing physiology, Zool. Sci., 31, 653, 10.2108/zs140094
Shen, 1994, A human opsin-related gene that encodes a retinaldehyde binding protein, Biochemistry, 33, 13117, 10.1021/bi00248a022
Koyanagi, 2002, Amphioxus homologs of Go- coupled rhodopsin and peropsin having 11-cis- and all-trans-retinals as their chromophores, FEBS Lett., 531, 525, 10.1016/S0014-5793(02)03616-5
Okano, 1994, Pinopsin is a chicken pineal photoreceptive molecule, Nature, 372, 94, 10.1038/372094a0
Max, 1995, Pineal opsin: a nonvisual opsin expressed in chick pineal, Science, 267, 1502, 10.1126/science.7878470
Kawamura, 1997, Expression of visual and nonvisual opsins in American chameleon, Vis. Res., 37, 1867, 10.1016/S0042-6989(96)00309-4
Yoshikawa, 1994, Immunoreactivities to rhodopsin and rod/cone transducin antisera in the retina, pineal complex and deep brain of the bullfrog, Rana catesbeiana, Zool. Sci., 11, 675
Yokoyama, 1997, Cloning and characterization of the pineal gland-specific opsin gene of marine lamprey (Petromyzon marinus), Gene, 202, 89, 10.1016/S0378-1119(97)00458-7
Provencio, 1998, Melanopsin: an opsin in melanophores, brain, and eye, Proc. Natl. Acad. Sci. U. S. A., 95, 340, 10.1073/pnas.95.1.340
Provencio, 2000, A novel human opsin in the inner retina, J. Neurosci., 20, 600, 10.1523/JNEUROSCI.20-02-00600.2000
Panda, 2003, Melanopsin is required for non-image-forming photic responses in blind mice, Science, 301, 525, 10.1126/science.1086179
Miyashita, 2001, Expression of opsin molecule in cultured murine melanocyte, J. Investig. Dermatol. Symp. Proc., 6, 54, 10.1046/j.0022-202x.2001.00018.x
Lopes, 2010, Modulation of rhodopsin gene expression and signaling mechanisms evoked by endothelins in goldfish and murine pigment cell lines, Braz. J. Med. Biol. Res., 43, 828, 10.1590/S0100-879X2010007500087
Bellingham, 2002, Zebrafish melanopsin: isolation, tissue localisation and phylogenetic position, Brain Res. Mol. Brain Res., 107, 128, 10.1016/S0169-328X(02)00454-0
Oshima, 2001, Direct reception of light by chromatophores of lower vertebrates, Pigment Cell Res., 14, 312, 10.1034/j.1600-0749.2001.140502.x
Tsutsumi, 2009, Expressions of rod and cone photoreceptor-like proteins in human epidermis, Exp. Dermatol., 18, 567, 10.1111/j.1600-0625.2009.00851.x
Wicks, 2011, UVA phototransduction drives early melanin synthesis in human melanocytes, Curr. Biol., 21, 1906, 10.1016/j.cub.2011.09.047
Denda, 2008, Visible radiation affects epidermal permeability barrier recovery: selective effects of red and blue light, J. Invest. Dermatol., 28, 1335, 10.1038/sj.jid.5701168
Kojima, 2011, UV-sensitive photoreceptor protein OPN5 in humans and mice, PLoS One, 6, 10.1371/journal.pone.0026388
de Assis, 2016, The effect of white light on normal and malignant murine melanocytes: A link between opsins, clock genes, and melanogenesis, Biochim. Biophys. Acta, 1863, 1119, 10.1016/j.bbamcr.2016.03.001
Toh, 2016, Expression of peropsin in human skin is related to phototransduction of violet light in keratinocytes, Exp. Dermatol., 25, 1002, 10.1111/exd.13226
Lan, 2019, Opsin 3 is a key regulator of ultraviolet A-induced photoaging in human dermal fibroblast cells, Br. J. Dermatol., 182, 1228, 10.1111/bjd.18410
Kusumoto, 2020, OPN4 belongs to the photosensitive system of the human skin, Genes Cells, 25, 215, 10.1111/gtc.12751
Hinterhuber, 2004, RPE65 of retinal pigment epithelium, a putative receptor molecule for plasma retinol-binding protein, is expressed in human keratinocytes, J. Invest. Dermatol., 122, 406, 10.1046/j.0022-202X.2004.22216.x
Shichida, 2009, Evolution of opsins and phototransduction, Philos. Trans. R. Soc. B Biol. Sci., 364, 2881, 10.1098/rstb.2009.0051
Birge, 1990, Photophysics and molecular electronic applications of the rhodopsins, Annu. Rev. Phys. Chem., 41, 683, 10.1146/annurev.pc.41.100190.003343
Oesterhelt, 1973, Functions of a new photoreceptor membrane, Proc. Natl. Acad. Sci. U. S. A., 70, 2853, 10.1073/pnas.70.10.2853
Inoue, 2014, Molecular and evolutionary aspects of microbial sensory rhodopsins, Biochim. Biophys. Acta, 1837, 562, 10.1016/j.bbabio.2013.05.005
Kurihara, 2015, Microbial rhodopsins: wide distribution, rich diversity and great potential, Biophys. Physicobiol., 12, 121, 10.2142/biophysico.12.0_121
Cooper, 1979, Energy uptake in the first step of visual excitation, Nature, 282, 531, 10.1038/282531a0
Zhukovsky, 1989, Effect of carboxylic acid side chains on the absorption maximum of visual pigments, Science, 246, 928, 10.1126/science.2573154
Shichida, 1998, Visual pigment: G-protein-coupled receptor for light signals, Cell. Mol. Life Sci., 54, 1299, 10.1007/s000180050256
Kim, 2001, Wavelength dependent cis-trans isomerization in vision, Biochemistry, 40, 13774, 10.1021/bi0116137
Schoenlein, 1991, The first step in vision: femtosecond isomerization of rhodopsin, Science, 254, 412, 10.1126/science.1925597
Polli, 2010, Conical intersection dynamics of the primary photoisomerization event in vision, Nature, 467, 440, 10.1038/nature09346
Moiseyev, 2005, RPE65 is the isomerohydrolase in the retinoid visual cycle, Proc. Natl. Acad. Sci. U. S. A., 102, 12413, 10.1073/pnas.0503460102
Matsuyama, 2012, Photochemical properties of mammalian melanopsin, Biochemistry, 51, 5454, 10.1021/bi3004999
Koyanagi, 2005, Cephalochordate melanopsin: evolutionary linkage between invertebrate visual cells and vertebrate photosensitive retinal ganglion cells, Curr. Biol., 15, 1065, 10.1016/j.cub.2005.04.063
Sugihara, 2016, Absorption characteristics of vertebrate non-visual opsin, Opn3, PLoS One, 11, 10.1371/journal.pone.0161215
Solomon, 2007, The machinery of colour vision, Nat. Rev. Neurosci., 8, 276, 10.1038/nrn2094
Bellono, 2013, UV light phototransduction depolarizes human melanocytes, Channels, 7, 243, 10.4161/chan.25322
Bellono, 2013, UV light phototransduction activates transient receptor potential A1 ion channels in human melanocytes, Proc. Natl. Acad. Sci. U. S. A., 110, 2383, 10.1073/pnas.1215555110
Shen, 2011, Function of rhodopsin in temperature discrimination in Drosophila, Science, 331, 1333, 10.1126/science.1198904
Barlow, 1988, The thermal limit to seeing, Nature, 334, 296, 10.1038/334296a0
Barlow, 1993, On the molecular origin of photoreceptor noise, Nature, 366, 64, 10.1038/366064a0
Guo, 2017, Probing the remarkable thermal kinetics of visual rhodopsin with E181Q and S186A mutants, J. Chem. Phys., 146, 215104, 10.1063/1.4984818
Sokabe, 2016, A switch in thermal preference in Drosophila larvae depends on multiple rhodopsins, Cell Rep., 17, 336, 10.1016/j.celrep.2016.09.028
Pérez-Cerezales, 2015, Involvement of opsins in mammalian sperm thermotaxis, Sci. Rep., 5, 16146, 10.1038/srep16146
Roy, 2020, Rhodopsin and melanopsin coexist in mammalian sperm cell and activate different signaling pathways for thermotaxis, Sci. Rep., 10, 112, 10.1038/s41598-019-56846-5
Moraes, 2017, Melanopsin, a canonical light receptor, mediates thermal activation of clock genes, Sci. Rep., 7, 13977, 10.1038/s41598-017-13939-3
Bellono, 2014, UV light activates a Galphaq/11-coupled phototransduction pathway in human melanocytes, J. Gen. Physiol., 143, 203, 10.1085/jgp.201311094
Sugiyama, 2014, Light-induced rapid Ca2+ response and MAPK phosphorylation in the cells heterologously expressing human OPN5, Sci. Rep., 4, 5352, 10.1038/srep05352
de Assis, 2017, Heat shock antagonizes UVA- induced responses in murine melanocytes and melanoma cells: an unexpected interaction, Photochem. Photobiol. Sci., 16, 633, 10.1039/c6pp00330c
Hu, 2017, Induction of retinal- dependent calcium influx in human melanocytes by UVA or UVB radiation contributes to the stimulation of melanosome transfer, Cell Prolif., 50, 10.1111/cpr.12372
Castellano-Pellicena, 2019, Does blue light restore human epidermal barrier function via activation of opsin during cutaneous wound healing? Lasers Surg, Med., 51, 370
Lan, 2019, Opsin 3 is a key regulator of ultraviolet A-induced photoaging in human dermal fibroblast cells, Br. J. Dermatol., 182, 1228, 10.1111/bjd.18410
Wang, 2020, Opsin3 downregulation induces apoptosis of human epidermal 509 melanocytes via mitochondrial pathway, Photochem. Photobiol., 96, 83, 10.1111/php.13178
de Assis, 2020, Melanopsin mediates UVA-dependent modulation of proliferation, pigmentation, apoptosis, and molecular clock in normal and malignant melanocytes, BBA – Mol. Cell. Res., 1867, 118789
Dumbuya, 2020, Cross talk between calcium and ROS regulates the UVA-induced melanin response in human melanocytes, FASEB J., 34, 11605, 10.1096/fj.201903024R
Buhr, 2019, Neuropsin (OPN5) mediates local light-dependent induction of circadian clock genes and circadian photoentrainment in exposed murine skin, Curr. Biol., 29, 3478, 10.1016/j.cub.2019.08.063
Fan, 2018, External light activates hair follicle stem cells through eyes via an ipRGC-SCN-sympathetic neural pathway, Proc. Natl. Acad. Sci. U. S. A., 115, E6880, 10.1073/pnas.1719548115
Leung, 2020, Functions of opsins in Drosophila taste, Curr. Biol., 30, 1367, 10.1016/j.cub.2020.01.068
Wehling, 2018, Rapid actions of aldosterone revisited: receptors in the limelight, J. Steroid Biochem. Mol. Biol., 176, 94, 10.1016/j.jsbmb.2017.01.016