Down-regulation of TRPM6-mediated magnesium influx by cyclosporin A

Naunyn Schmiedebergs Arch Pharmacol. 2008 Jun;377(4-6):333-43. doi: 10.1007/s00210-007-0212-4. Epub 2007 Nov 17.

Abstract

Transient receptor potential melastatin 6 (TRPM6) is distributed along the apical membrane of the renal tubular cells and is involved in the reabsorption of magnesium. In this study, we show that TRPM6 expression is suppressed by cyclosporin A (CsA) via a down-regulation of c-Fos expression. TRPM6 was expressed in NRK-52E, but not in Madin-Darby canine kidney cells. In contrast, its homolog, TRPM7, was equally expressed in both cells. In NRK-52E cells, CsA dose-dependently decreased TRPM6 expression without affecting TRPM7 expression. Magnesium load measurements revealed the rise in the intracellular free magnesium concentration ([Mg2+]i) to be inhibited by CsA. The transfection of TRPM6 siRNA decreased TRPM6 expression without affecting TRPM7 expression and inhibited the elevation of [Mg2+]i. CsA did not affect the intracellular distribution of nuclear factor of activated T cells (NFATc). Furthermore, TRPM6 expression was not changed by a NFATc inhibitor. Next, we examined the effect of CsA on the transcription factors c-Fos and c-Jun. CsA decreased c-Fos expression without affecting c-Jun expression. The transfection of c-Fos siRNA suppressed TRPM6 expression without affecting TRPM7 expression. We suggest that CsA decreases TRPM6 expression mediated by inhibition of c-Fos transcription, resulting in a decrease of renal Mg2+ reabsorption.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cyclosporine / administration & dosage
  • Cyclosporine / pharmacology*
  • Dogs
  • Dose-Response Relationship, Drug
  • Down-Regulation / drug effects
  • Immunosuppressive Agents / administration & dosage
  • Immunosuppressive Agents / pharmacology*
  • Kidney / metabolism
  • Magnesium / metabolism*
  • NFATC Transcription Factors / drug effects
  • NFATC Transcription Factors / metabolism
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / metabolism
  • RNA, Small Interfering / metabolism
  • Rats
  • TRPM Cation Channels / drug effects*
  • TRPM Cation Channels / metabolism
  • Transcription, Genetic / drug effects
  • Transfection

Substances

  • Immunosuppressive Agents
  • NFATC Transcription Factors
  • Proto-Oncogene Proteins c-fos
  • RNA, Small Interfering
  • TRPM Cation Channels
  • TRPM6 protein, rat
  • Cyclosporine
  • Trpm7 protein, rat
  • Magnesium