H. Kahr and R. Schindl contributed equally to the work.
CaT1 knock-down strategies fail to affect CRAC channels in mucosal-type mast cells
Article first published online: 4 MAY 2004
The Journal of Physiology
Volume 557, Issue 1, pages 121–132, May 2004
How to Cite
Kahr, H., Schindl, R., Fritsch, R., Heinze, B., Hofbauer, M., Hack, M. E., Mörtelmaier, M. A., Groschner, K., Peng, J.-B., Takanaga, H., Hediger, M. A. and Romanin, C. (2004), CaT1 knock-down strategies fail to affect CRAC channels in mucosal-type mast cells. The Journal of Physiology, 557: 121–132. doi: 10.1113/jphysiol.2004.062653
- Issue published online: 4 MAY 2004
- Article first published online: 4 MAY 2004
- (Resubmitted 11 February 2004; accepted after revision 11 March 2004; first published online 12 March 2004)
CaT1, the calcium transport protein 1 encoded by TRPV6, is able to generate a Ca2+ conductance similar but not identical to the classical CRAC current in mucosal-type mast cells. Here we show that CaT1-derived Ca2+ entry into HEK293 cells is effectively inhibited either by expression of various dominant negative N-terminal fragments of CaT1 (N334-CaT1, N198-CaT1 and N154-CaT1) or by antisense suppression. By contrast, the endogenous CRAC current of the mast cells was unaffected by CaT1 antisense and siRNA knockdown but markedly suppressed by two (N334-CaT1, N198-CaT1) of the dominant negative N-CaT1 fragments. Inhibition of CRAC current was not an unspecific, toxic effect, as inward rectifier K+ and MagNuM currents of the mast cells were not significantly affected by these N-CaT1 fragments. The shortest N154-CaT1 fragment inhibited CaT1-derived currents in mast cells, but failed to inhibit CRAC currents. Thus, the structural requirements of rCaT N-terminal fragments for inhibition of rCaT1 and CRAC channels are different. These results together with the lack of CaT1 antisense and siRNA effects on currents render it unlikely that CaT1 is a component of native CRAC channels in mast cells. The data further demonstrate a novel strategy for CRAC current inhibition by an N-terminal structure of CaT1.