TRPV6 modulates proliferation of human pancreatic neuroendocrine BON-1 tumour cells

Biosci Rep. 2016 Aug 24;36(4):e00372. doi: 10.1042/BSR20160106. Print 2016 Aug.

Abstract

Highly Ca(2+) permeable receptor potential channel vanilloid type 6 (TRPV6) modulates a variety of biological functions including calcium-dependent cell growth and apoptosis. So far, the role of TRPV6 in controlling growth of pancreatic neuroendocrine tumour (NET) cells is unknown. In the present study, we characterize the expression of TRPV6 in pancreatic BON-1 and QGP-1 NET cells. Furthermore, we evaluate the impact of TRPV6 on intracellular calcium, the activity of nuclear factor of activated T-cells (NFAT) and proliferation of BON-1 cells. TRPV6 expression was assessed by real-time PCR and Western blot. TRPV6 mRNA expression and protein production were down-regulated by siRNA. Changes in intracellular calcium levels were detected by fluorescence calcium imaging (fura-2/AM). NFAT activity was studied by NFAT reporter assay; cell proliferation by bromodeoxyuridine (BrdU), MTT and propidium iodine staining. TRPV6 mRNA and protein are present in BON-1 and QGP-1 NET-cells. Down-regulation of TRPV6 attenuates BON-1 cell proliferation. TRPV6 down-regulation is associated with decreased Ca(2+) response pattern and reduced NFAT activity. In conclusion, TRPV6 is expressed in pancreatic NETs and modulates cell proliferation via Ca(2+)-dependent mechanism, which is accompanied by NFAT activation.

Keywords: BON-1; QGP-1; TRPV6; calcium; neuroendocrine tumour; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology
  • Calcium / metabolism
  • Calcium Channels / metabolism*
  • Cell Line, Tumor
  • Cell Proliferation / physiology*
  • Down-Regulation / physiology
  • Humans
  • NFATC Transcription Factors / metabolism
  • Neuroendocrine Tumors / metabolism*
  • Neuroendocrine Tumors / pathology*
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology*
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • TRPV Cation Channels / metabolism*

Substances

  • Calcium Channels
  • NFATC Transcription Factors
  • RNA, Messenger
  • RNA, Small Interfering
  • TRPV Cation Channels
  • TRPV6 protein, human
  • Calcium