ORAI1 Ca(2+) channels control endothelin-1-induced mitogenesis and melanogenesis in primary human melanocytes

J Invest Dermatol. 2012 May;132(5):1443-51. doi: 10.1038/jid.2011.478. Epub 2012 Feb 9.

Abstract

UV radiation of the skin triggers keratinocytes to secrete endothelin-1 (ET-1) that binds to endothelin receptors on neighboring melanocytes. Melanocytes respond with a prolonged increase in intracellular Ca(2+) concentration ([Ca(2+)](i)), which is necessary for proliferation and melanogenesis. A major fraction of the Ca(2+) signal is caused by entry through Ca(2+)-permeable channels of unknown identity in the plasma membrane. ORAI Ca(2+) channels are molecular determinants of Ca(2+) release-activated Ca(2+) (CRAC) channels and are expressed in many tissues. Here, we show that ORAI1-3 and their activating partners stromal interaction molecules 1 and 2 (STIM1 and STIM2) are expressed in human melanocytes. Although ORAI1 is the predominant ORAI isoform, STIM2 mRNA expression exceeds STIM1. Inhibition of ORAI1 by 2-aminoethoxydiphenyl borate (2-APB) or downregulation of ORAI1 by small interfering RNA (siRNA) reduced Ca(2+) entry and CRAC current amplitudes in activated melanocytes. In addition, suppression of ORAI1 caused reduction in the ET-1-induced cellular viability, melanin synthesis, and tyrosinase activity. Our results imply a role for ORAI1 channels in skin pigmentation and their potential involvement in UV-induced stress responses of the human skin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron Compounds / pharmacology
  • Calcium / metabolism
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism*
  • Cell Adhesion Molecules / metabolism
  • Cells, Cultured
  • Down-Regulation
  • Endothelin-1 / metabolism*
  • Humans
  • Melanins / biosynthesis*
  • Melanocytes / metabolism
  • Melanocytes / physiology*
  • Membrane Proteins / metabolism
  • Mitosis / physiology*
  • Neoplasm Proteins / metabolism
  • ORAI1 Protein
  • ORAI2 Protein
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology
  • Stromal Interaction Molecule 1
  • Stromal Interaction Molecule 2

Substances

  • Boron Compounds
  • Calcium Channels
  • Cell Adhesion Molecules
  • Endothelin-1
  • Melanins
  • Membrane Proteins
  • Neoplasm Proteins
  • ORAI1 Protein
  • ORAI1 protein, human
  • ORAI2 Protein
  • ORAI2 protein, human
  • Orai3 protein, human
  • RNA, Messenger
  • RNA, Small Interfering
  • STIM1 protein, human
  • STIM2 protein, human
  • Stromal Interaction Molecule 1
  • Stromal Interaction Molecule 2
  • 2-aminoethoxydiphenyl borate
  • Calcium