Transient receptor potential channel TRPM8 agonists stimulate calcium influx and neurotensin secretion in neuroendocrine tumor cells

Neuroendocrinology. 2007;85(2):81-92. doi: 10.1159/000101693. Epub 2007 Apr 5.

Abstract

TRPM8 is a member of the melastatin-type transient receptor potential ion channel family. Activation by cold or by agonists (menthol, icilin) induces a transient rise in intracellular free calcium concentration ([Ca(2+)](i)). Our previous study demonstrated that Ca(2+)-permeable cation channels play a role in IGF-1-induced secretion of chromogranin A in human neuroendocrine tumor (NET) cell line BON [Mergler et al.: Neuroendocrinology 2006;82:87-102]. Here, we extend our earlier study by investigating the expression of TRPM8 and characterizing its impact on [Ca(2+)](i) and the secretion of neurotensin (NT). We identified TRPM8 expression in NET BON cells by RT-PCR, Western blotting and immunofluorescence staining. Icilin increased [Ca(2+)](i) in TRPM8-transfected human embryonic kidney cells (HEK293) but not in mock-transfected cells. Icilin and menthol induced Ca(2+) transients in BON cells as well as in primary NET cell cultures of two different pancreatic NETs as detected by single cell fluorescence imaging. Icilin increased non-selective cation channel currents in BON cells as detected by patch-clamp recordings. This activation was associated with increased NT secretion. Taken together, this study demonstrates for the first time the expression TRPM8 in NET cells and its role in regulating [Ca(2+)](i) and NT secretion. The regulation of NT secretion in NETs by TRPM8 may have a potential clinical implication in diagnosis or therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism*
  • Humans
  • Membrane Potentials / drug effects
  • Menthol / pharmacology*
  • Models, Biological
  • Neuroendocrine Tumors / pathology*
  • Neurotensin / metabolism*
  • Pancreatic Neoplasms / pathology*
  • Pyrimidinones / pharmacology*
  • TRPM Cation Channels / agonists*
  • TRPM Cation Channels / metabolism
  • Tumor Cells, Cultured

Substances

  • Pyrimidinones
  • TRPM Cation Channels
  • TRPM8 protein, human
  • Menthol
  • Neurotensin
  • icilin
  • Calcium