Abstract
Hydrogen peroxide (H2O2) may have a biphasic effect on melanin synthesis and melanosome transfer. High H2O2 concentrations are involved in impaired melanosome transfer in vitiligo. However, low H2O2 concentration promotes the beneficial proliferation and migration of melanocytes. The aim of this study was to explore low H2O2 and its mechanism in melanosome transfer, protease-activated receptor-2 (PAR-2) expression and calcium balance. Melanosomes were fluorescein-labeled for clear visualization of their transfer. The expression of protease-activated receptor-2 (PAR-2) in keratinocytes was determined by western blot analysis. Flow cytometry was employed to evaluate the effects of H2O2 on calcium levels in keratinocytes. Fluorescence microscopy showed the upregulation of melanosome transfer into keratinocytes following 0.3 mM H2O2 treatment in the co-cultures rather than in the untreated control groups, which was associated with higher expression of PAR-2 protein and increased calcium concentration. The addition of a PAR-2 antagonist inhibited the positive activity of H2O2 and calcium flow in keratinocytes. When calcium flow was blocked by a calcium chelator, the addition of H2O2 did not increase the PAR-2 expression level in keratinocytes, therefore, inhibiting dendrite formation and melanosome transfer. Low H2O2 concentration promotes melanosome transfer with increased PAR-2 expression level and calcium concentration in keratinocytes. In addition, the interaction between melanocytes and keratinocytes is more beneficial to enhance calcium levels in keratinocytes which mediate melanin transfer. Moreover, low H2O2 concentration promotes dendrite formation, in which extracellular calcium and Par-2 were involved.
Similar content being viewed by others
References
AlGhamdi KM, Kumar A, Ashour AE, AlGhamdi AA (2015) A comparative study of the effects of different low-level lasers on the proliferation, viability, and migration of human melanocytes in vitro. Lasers Med Sci 30:1541–1551. doi:10.1007/s10103-015-1758-x
Alkhateeb A, Fain PR, Thody A, Bennett DC, Spritz RA (2003) Epidemiology of vitiligo and associated autoimmune diseases in Caucasian probands and their families. Pigment Cell Res 16:208–214
Braga V, Harwood AJ (2001) Super glue. Nat Cell Biol 3:E168–E170. doi:10.1038/35083128
Choi EJ, Kang YG, Kim J, Hwang JK (2011) Macelignan inhibits melanosome transfer mediated by protease-activated receptor-2 in keratinocytes. Biol Pharm Bull 34:748–754
Choi HI, Sohn KC, Hong DK, Lee Y, Kim CD, Yoon TJ, Park JW, Jung S, Lee JH, Lee YH (2014) Melanosome uptake is associated with the proliferation and differentiation of keratinocytes. Arch Dermatol Res 306:59–66. doi:10.1007/s00403-013-1422-x
Duval C, Smit NP, Kolb AM, Regnier M, Pavel S, Schmidt R (2002) Keratinocytes control the pheo/eumelanin ratio in cultured normal human melanocytes. Pigment Cell Res 15:440–446
Gibbons NC, Wood JM, Rokos H, Schallreuter KU (2006) Computer simulation of native epidermal enzyme structures in the presence and absence of hydrogen peroxide (H2O2): potential and pitfalls. J Invest Dermatol 126:2576–2582. doi:10.1038/sj.jid.5700612
Gniadecki R, Gajkowska B (2003) Intracellular calcium pool emptying induces DNA synthesis in HaCaT keratinocytes. Exp Dermatol 12:453–459
Hirobe T (2011) How are proliferation and differentiation of melanocytes regulated? Pigment Cell Melanoma Res 24:462–478. doi:10.1111/j.1755-148X.2011.00845.x
Ito Y, Kanamaru A, Tada A (2006) Centaureidin promotes dendrite retraction of melanocytes by activating Rho. Biochim Biophys Acta 1760:487–494. doi:10.1016/j.bbagen.2006.01.003
Joshi PG, Nair N, Begum G, Joshi NB, Sinkar VP, Vora S (2007) Melanocyte-keratinocyte interaction induces calcium signalling and melanin transfer to keratinocytes. Pigment Cell Res 20:380–384. doi:10.1111/j.1600-0749.2007.00397.x
Khan R, Satyam A, Gupta S, Sharma VK, Sharma A (2009) Circulatory levels of antioxidants and lipid peroxidation in Indian patients with generalized and localized vitiligo. Arch Dermatol Res 301:731–737. doi:10.1007/s00403-009-0964-4
Kleszczynski K, Ernst IM, Wagner AE, Kruse N, Zillikens D, Rimbach G, Fischer TW (2013) Sulforaphane and phenylethyl isothiocyanate protect human skin against UVR-induced oxidative stress and apoptosis: role of Nrf2-dependent gene expression and antioxidant enzymes. Pharmacol Res 78:28–40. doi:10.1016/j.phrs.2013.09.009
Lei TC, Vieira WD, Hearing VJ (2002) In vitro migration of melanoblasts requires matrix metalloproteinase-2: implications to vitiligo therapy by photochemotherapy. Pigment Cell Res 15:426–432
Lei TC, Virador VM, Vieira WD, Hearing VJ (2002) A melanocyte-keratinocyte coculture model to assess regulators of pigmentation in vitro. Anal Biochem 305:260–268. doi:10.1006/abio.2002.5665
Lu-yan T, Wen-wen F, Lei-hong X, Yi J, Zhi-zhong Z (2006) Topical tacalcitol and 308-nm monochromatic excimer light: a synergistic combination for the treatment of vitiligo. Photodermatol Photoimmunol Photomed 22:310–314. doi:10.1111/j.1600-0781.2006.00250.x
Macfarlane SR, Sloss CM, Cameron P, Kanke T, McKenzie RC, Plevin R (2005) The role of intracellular Ca2+ in the regulation of proteinase-activated receptor-2 mediated nuclear factor kappa B signalling in keratinocytes. Br J Pharmacol 145:535–544. doi:10.1038/sj.bjp.0706204
Miyazaki K (2004) Novel approach for evaluation of estrogenic and anti-estrogenic activities of genistein and daidzein using B16 melanoma cells and dendricity assay. Pigment Cell Res 17:407–412. doi:10.1111/j.1600-0749.2004.00167.x
Moretti S, Nassini R, Prignano F, Pacini A, Materazzi S, Naldini A, Simoni A, Baroni G, Pellerito S, Filippi I, Lotti T, Geppetti P, Massi D (2009) Protease-activated receptor-2 downregulation is associated to vitiligo lesions. Pigment Cell Melanoma Res 22:335–338. doi:10.1111/j.1755-148X.2009.00562.x
Oh SH, Kim JY, Kim MR, Do JE, Shin JY, Hann SK (2012) DKK1 is highly expressed in the dermis of vitiligo lesion: is there association between DKK1 and vitiligo? J Dermatol Sci 66:163–165. doi:10.1016/j.jdermsci.2012.01.010
Park HY, Kosmadaki M, Yaar M, Gilchrest BA (2009) Cellular mechanisms regulating human melanogenesis. Cell Mol Life Sci 66:1493–1506. doi:10.1007/s00018-009-8703-8
Schallreuter KU, Moore J, Wood JM, Beazley WD, Gaze DC, Tobin DJ, Marshall HS, Panske A, Panzig E, Hibberts NA (1999) In vivo and in vitro evidence for hydrogen peroxide (H2O2) accumulation in the epidermis of patients with vitiligo and its successful removal by a UVB-activated pseudocatalase. J Investig Dermatol Symp Proc 4:91–96
Schallreuter KU, Rubsam K, Chavan B, Zothner C, Gillbro JM, Spencer JD, Wood JM (2006) Functioning methionine sulfoxide reductases A and B are present in human epidermal melanocytes in the cytosol and in the nucleus. Biochem Biophys Res Commun 342:145–152. doi:10.1016/j.bbrc.2006.01.124
Schallreuter KU, Salem MA, Holtz S, Panske A (2013) Basic evidence for epidermal H2O2/ONOO(−)-mediated oxidation/nitration in segmental vitiligo is supported by repigmentation of skin and eyelashes after reduction of epidermal H2O2 with topical NB-UVB-activated pseudocatalase PC-KUS. FASEB J 27:3113–3122. doi:10.1096/fj.12-226779
Schallreuter KU, Wazir U, Kothari S, Gibbons NC, Moore J, Wood JM (2004) Human phenylalanine hydroxylase is activated by H2O2: a novel mechanism for increasing the l-tyrosine supply for melanogenesis in melanocytes. Biochem Biophys Res Commun 322:88–92. doi:10.1016/j.bbrc.2004.07.082
Scott G, Deng A, Rodriguez-Burford C, Seiberg M, Han R, Babiarz L, Grizzle W, Bell W, Pentland A (2001) Protease-activated receptor 2, a receptor involved in melanosome transfer, is upregulated in human skin by ultraviolet irradiation. J Invest Dermatol 117:1412–1420. doi:10.1046/j.0022-202x.2001.01575.x
Scott G, Leopardi S, Parker L, Babiarz L, Seiberg M, Han R (2003) The proteinase-activated receptor-2 mediates phagocytosis in a Rho-dependent manner in human keratinocytes. J Invest Dermatol 121:529–541. doi:10.1046/j.1523-1747.2003.12427.x
Seiberg M (2001) Keratinocyte-melanocyte interactions during melanosome transfer. Pigment Cell Res 14:236–242
Seiberg M, Paine C, Sharlow E, Andrade-Gordon P, Costanzo M, Eisinger M, Shapiro SS (2000) The protease-activated receptor 2 regulates pigmentation via keratinocyte-melanocyte interactions. Exp Cell Res 254:25–32. doi:10.1006/excr.1999.4692
Sharlow ER, Paine CS, Babiarz L, Eisinger M, Shapiro S, Seiberg M (2000) The protease-activated receptor-2 upregulates keratinocyte phagocytosis. J Cell Sci 113(Pt 17):3093–3101
Tang L, Li J, Lin X, Wu W, Kang K, Fu W (2012) Oxidation levels differentially impact melanocytes: low versus high concentration of hydrogen peroxide promotes melanin synthesis and melanosome transfer. Dermatology 224:145–153. doi:10.1159/000336777
Tarafder AK, Bolasco G, Correia MS, Pereira FJ, Iannone L, Hume AN, Kirkpatrick N, Picardo M, Torrisi MR, Rodrigues IP, Ramalho JS, Futter CE, Barral DC, Seabra MC (2014) Rab11b mediates melanin transfer between donor melanocytes and acceptor keratinocytes via coupled exo/endocytosis. J Invest Dermatol 134:1056–1066. doi:10.1038/jid.2013.432
Tu CL, Chang W, Xie Z, Bikle DD (2008) Inactivation of the calcium sensing receptor inhibits E-cadherin-mediated cell-cell adhesion and calcium-induced differentiation in human epidermal keratinocytes. J Biol Chem 283:3519–3528. doi:10.1074/jbc.M708318200
Wolff K, Goldsmith L, Katz S, Gilchrest B, Paller A, Leffell D (2007) Fitzpatrick’s dermatology in general medicine, 7th edn. Mac Graw Hill, USA
Wu JB, Song NN, Wei XB, Guan HS, Zhang XM (2008) Protective effects of paeonol on cultured rat hippocampal neurons against oxygen-glucose deprivation-induced injury. J Neurol Sci 264:50–55. doi:10.1016/j.jns.2007.06.057
Pelle E, Mammone T, Maes D, Frenkel K (2005) Keratinocytes act as a source of reactive oxygen species by transferring hydrogen peroxide to melanocytes. J invest dermatol 124(4):793–797. doi:10.1111/j.0022-202X.2005.23661.x
Acknowledgments
The present work was sponsored by the Science and Technology Commission of Shanghai Municipality (Grant No. 13401902600).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Ethical approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee of Huashan Hospital of Fudan University and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Informed consent
Informed consent was obtained from all individual participants included in the study.
Conflict of interest
The authors declare that they have no conflict of interest.
Rights and permissions
About this article
Cite this article
Li, J., Tang, LY., Fu, WW. et al. Low-concentration hydrogen peroxide can upregulate keratinocyte intracellular calcium and PAR-2 expression in a human keratinocyte–melanocyte co-culture system. Arch Dermatol Res 308, 723–731 (2016). https://doi.org/10.1007/s00403-016-1692-1
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00403-016-1692-1