Ionic currents underlying HTRP3 mediated agonist-dependent Ca2+ influx in stably transfected HEK293 cells.

Abstract:

:hTrp3 is a human homologue of the Drosophila gene responsible for a transient receptor potential (trp) mutation. When stably expressed in HEK293 cells, hTrp3 formed ion channels that were active under resting conditions but could be further stimulated by carbachol or ATP via endogenous muscarinic or purinergic receptors, respectively. Agonist evoked currents reversed polarity near 0 mV in physiological ionic conditions and were associated with a significant increase in the current variance. These results suggest the involvement of a non-selective cation channel with relatively large unitary amplitude. Consistent with this, resolved unitary events had a conductance of approximately 60 pS in the negative voltage range and an extrapolated reversal potential near 0 mV.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Hurst RS,Zhu X,Boulay G,Birnbaumer L,Stefani E

doi

10.1016/s0014-5793(98)00035-0

subject

Has Abstract

pub_date

1998-02-06 00:00:00

pages

333-8

issue

3

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(98)00035-0

journal_volume

422

pub_type

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