Trp proteins form store-operated cation channels in human vascular endothelial cells

FEBS Lett. 1998 Oct 16;437(1-2):101-6. doi: 10.1016/s0014-5793(98)01212-5.

Abstract

Members of the Trp protein family have been suggested as the structural basis of store-operated cation conductances. With this study, we provide evidence for the expression of three isoforms of Trp (hTrp1, 3 and 4) in human umbilical vein endothelial cells (HUVEC). The role of Trp proteins in store regulation of endothelial membrane conductances was tested by expression of an N-terminal fragment of hTrp3 (N-TRP) which exerts a dominant negative effect on Trp channel function presumably due to suppression of channel assembly. Depletion of intracellular Ca2+ stores with IP3 (100 microM) or thapsigargin (100 nM) induced a substantial cation conductance in sham-transfected HUVEC as well as in HUVEC transfected with hTrp3. In contrast, HUVEC transfected with N-TRP failed to exhibit store-operated currents. Our results suggest the involvement of Trp related proteins in the store-operated cation conductance of human vascular endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium Channels / genetics
  • Calcium Channels / metabolism*
  • Cells, Cultured
  • Endothelium, Vascular / metabolism*
  • Humans
  • Patch-Clamp Techniques
  • TRPC Cation Channels
  • Thapsigargin / pharmacology
  • Transfection
  • Umbilical Veins

Substances

  • Calcium Channels
  • TRPC Cation Channels
  • transient receptor potential cation channel, subfamily C, member 1
  • Thapsigargin