1. Academic Validation
  2. UV-induced DNA Damage in Skin is Reduced by CaSR Inhibition

UV-induced DNA Damage in Skin is Reduced by CaSR Inhibition

  • Photochem Photobiol. 2022 Sep;98(5):1157-1166. doi: 10.1111/php.13615.
Chen Yang 1 Mark Stephen Rybchyn 1 2 Warusavithana Gunawardena Manori De Silva 1 Jim Matthews 3 Andrew J A Holland 4 Arthur David Conigrave 5 Rebecca Sara Mason 1 5
Affiliations

Affiliations

  • 1 Department of Physiology and Bosch Institute, School of Medical Sciences, University of Sydney, NSW, Australia.
  • 2 School of Chemical Engineering, University of New South Wales, Sydney, NSW, Australia.
  • 3 Sydney Informatics Hub, University of Sydney, Sydney, NSW, Australia.
  • 4 Douglas Cohen Department of Paediatric Surgery, Faculty of Medicine and Health, The Children's Hospital at Westmead Clinical School, The University of Sydney School of Medicine, Sydney, NSW, Australia.
  • 5 School of Life and Environmental Sciences, Charles Perkins Centre (D17), University of Sydney, Sydney, NSW, 2006, Australia.
Abstract

The epidermis maintains a cellular calcium gradient that supports keratinocyte differentiation from its basal layers (low) to outer layers (high) leading to the development of the stratum corneum, which resists penetration of UV radiation. The calcium-sensing receptor (CaSR) expressed in keratinocytes responds to the calcium gradient with signals that promote differentiation. In this study, we investigated whether the CaSR is involved more directly in protection from UV damage in studies of human keratinocytes in primary culture and in mouse skin studied in vivo. siRNA-directed reductions in CaSR protein levels in human keratinocytes significantly reduced UV-induced direct cyclobutane pyrimidine dimers (CPD) by ~80% and oxidative DNA damage (8-OHdG) by ~65% compared with control transfected cells. Similarly, in untransfected cells, the CaSR negative modulator, NPS-2143 (500 nm), reduced UV-induced CPD and 8-OHdG by ~70%. NPS-2143 also enhanced DNA repair and reduced Reactive Oxygen Species (ROS) by ~35% in UV-exposed keratinocytes, consistent with reduced DNA damage after UV exposure. Topical application of NPS-2143 also protected hairless Skh:hr1 mice from UV-induced CPD, oxidative DNA damage and inflammation, similar to the reductions observed in response to the well-known photoprotection agent 1,25(OH)2 D3 (calcitriol). Thus, negative modulators of the CaSR offer a new approach to reducing UV-induced skin damage.

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