Channel name | TRPC71,2 |
Description | Cardiac TRP channel |
Other names | TRP7 |
Molecular information | Human unigene: Hs0.283104, chr. 5q31.1 |
Mouse unigene: Mm0.62409, chr. 13 B2 | |
Associated subunits | TRPC3, TRPC6, calmodulin, FKBP12 |
Functional assays | Patch-clamp, calcium imaging |
Current | Inwardly and outwardly rectifying, nonselective cation current |
Conductance | 50pS (0–100 mV); 25pS (–100 to 0 mV) |
Ion selectivity | PNa/PCa ∼1:1.9 |
Activation | Sensitive to intracellular Ca2+ |
Inactivation | Not established |
Activators | DAG and analogs (100 μM) |
Gating inhibitors | None |
Blockers | La3+ (100 μM), SKF96365 (25 μM), 0.1–0.4 mM [Ca2+]o |
Radioligands | None |
Channel distribution | Heart, lung, eye, brain, spleen, testis |
Physiological functions | Cation influx in response to Gq activation |
Mutations and pathophysiology | Not established |
Pharmacological significance | Extracellular ATP (possibly via purinergic receptors), modulated by intracellular calcium, PKC |
chr., chromosome.
↵1. Okada T, Inoue R, Yamazaki K, Maeda A, Kurosaki T, Yamakuni T, Tanaka I, Shimizu S, Ikenaka K, Imoto K, et al. (1999) Molecular and functional characterization of a novel mouse transient receptor potential protein homologue TRP7. Ca2+-permeable cation channel that is constitutively activated and enhanced by stimulation of G protein-coupled receptor. J Biol Chem 274:27359-27370
↵2. Shi J, Mori E, Mori Y, Mori M, Li J, Ito Y, and Inoue R (2004) Multiple regulation by calcium of murine homologues of transient receptor potential proteins TRPC6 and TRPC7 expressed in HEK293 cell. J Physiol 561:415-432