Literature DB >> 16298688

Low UVA doses activate the transcription factor NFAT in human fibroblasts by a calcium-calcineurin pathway.

Cécile Mazière1, Patrice Morlière, Christophe Louandre, Marie-Alix Conte, Cathy Gomilla, René Santus, Franck Antonicelli, William Hornebeck, Jean-Claude Mazière.   

Abstract

UVA radiation induces an inflammatory response as observed in erythema, and the cytokine genes involved in this response are under the control of the transcription factor NFAT (nuclear factor of activated T lymphocytes). The effects of UVA on NFAT DNA binding activity were investigated in cultured human fibroblasts. A dose-dependent increase was observed within the range of 0.6-4.5 J/cm2 UVA. Beyond this value, the activity decreased and a value of 60% of control was found at 13.5 J/cm2. The enhancement of NFAT activity was transient and peaked 45 min after irradiation. Furthermore, immunoblot analysis demonstrated a nuclear translocation of NFAT under low UVA doses. Concomitantly, as assessed by the fluorescent probe Fluo3, UVA induced an increase in intracellular free calcium, with a maximum increase found at 9 J/cm2. The UVA-induced activation of NFAT was prevented by the intracellular calcium trapping drug BAPTA, whereas the extracellular calcium chelator EGTA had no significant effect. In addition, the calcineurin inhibitors cyclosporin A and FK506 both prevented the UVA-induced NFAT activation. Furthermore, the antioxidant vitamin E prevented the UVA-induced increase in both intracellular free calcium and NFAT binding activity. Finally, the cytotoxicity of UVA was enhanced in the presence of the inhibitors cyclosporin and FK506, suggesting that the activation of NFAT might play a protective role after the UVA-induced oxidative stress. These results demonstrate that UVA activates the calcium-calcineurin signaling pathway of NFAT activation, that the calcium ions are mainly released from intracellular stores, and that the increase in calcium is, at least partially, due to the oxidative stress generated under UVA. Because NFAT regulates several genes implicated in the inflammatory response, the enhancement of NFAT activity by low UVA doses might be interpreted in view of the proinflammatory action of solar radiation.

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Year:  2005        PMID: 16298688     DOI: 10.1016/j.freeradbiomed.2005.08.003

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  4 in total

1.  7-Dehydrocholesterol enhances ultraviolet A-induced oxidative stress in keratinocytes: roles of NADPH oxidase, mitochondria, and lipid rafts.

Authors:  Antonio Valencia; Anpuchchelvi Rajadurai; A Bjorn Carle; Irene E Kochevar
Journal:  Free Radic Biol Med       Date:  2006-09-09       Impact factor: 7.376

2.  Mechanisms of Action Involved in Ozone Therapy: Is healing induced via a mild oxidative stress?

Authors:  Masaru Sagai; Velio Bocci
Journal:  Med Gas Res       Date:  2011-12-20

Review 3.  Protein kinases and transcription factors activation in response to UV-radiation of skin: implications for carcinogenesis.

Authors:  César López-Camarillo; Elena Aréchaga Ocampo; Mavil López Casamichana; Carlos Pérez-Plasencia; Elizbeth Alvarez-Sánchez; Laurence A Marchat
Journal:  Int J Mol Sci       Date:  2011-12-23       Impact factor: 5.923

4.  NFAT regulates induction of COX-2 and apoptosis of keratinocytes in response to ultraviolet radiation exposure.

Authors:  R J Flockhart; B L Diffey; P M Farr; J Lloyd; N J Reynolds
Journal:  FASEB J       Date:  2008-08-15       Impact factor: 5.191

  4 in total

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