Channel name | TRPV61,2,3 |
Description | Calcium-selective TRP channel |
Other names | ECaC2, CaT1 |
Molecular information | Human unigene: Hs0.302740, chr. 7q33–34 |
Mouse unigene: Mm0.296889, chr. 6 | |
Associated subunits | Not established |
Functional assays | Patch-clamp, calcium imaging |
Current | Inwardly rectifying, calcium-sensitive cation current |
Conductance | 42–58pS in calcium-free solution |
Erev in saline solution >50 mV | |
Ion selectivity | Ca2+ > Ba2+ > Sr2+ > Mn2+; PNa/PCa = 1:130 |
Activation | Constitutively active |
Inactivation | Not established |
Activators | None |
Gating inhibitors | None |
Blockers | Ruthenium red (5 μM), La3+ |
Radioligands | None |
Channel distribution | Kidney, intestine |
Physiological functions | Not established |
Mutations and pathophysiology | Not established |
Pharmacological significance | Not established |
Comments | One of only two known TRP channels (with TRPV5) that is relatively highly Ca2+-selective |
chr., chromosome.
↵1. Yue L, Peng JB, Hediger MA, and Clapham DE (2001) CaT1 manifests the pore properties of the calcium-release-activated calcium channel. Nature (Lond) 410:705-709
↵2. Bodding M and Flockerzi V (2004) Ca2+ dependence of the Ca2+-selective TRPV6 channel. J Biol Chem 279:36546-36552
↵3. Lambers TT, Weidema AF, Nilius B, Hoenderop JG, and Bindels RJ (2004) Regulation of the mouse epithelial Ca2+ channel TRPV6 by the Ca2+-sensor calmodulin. J Biol Chem 279:28855-28861