The α1ECalcium Channel Exhibits Permeation Properties Similar to Low-Voltage-Activated Calcium Channels
Open Access
- 15 August 1996
- journal article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 16 (16), 4983-4993
- https://doi.org/10.1523/jneurosci.16-16-04983.1996
Abstract
The physiological and pharmacological properties of the α1E calcium (Ca) channel subtype do not exactly match any of the established categories described for native neuronal Ca currents. Many of the key diagnostic features used to assign cloned Ca channels to their native counterparts, however, are dependent on a number of factors, including cellular environment, β subunit coexpression, and modulation by second messengers and G-proteins. Here, by examining the intrinsic pore characteristics of a family of transiently expressed neuronal Ca channels, we demonstrate that the permeation properties of α1E closely resemble those described for a subset of low-threshold Ca channels. The α1A (P-/Q-type), α1B(N-type), and α1C (L-type) high-threshold Ca channels all exhibit larger whole-cell currents with barium (Ba) as the charge carrier as compared with Ca or strontium (Sr). In contrast, macroscopic α1E currents are largest in Sr, followed by Ca and then Ba. The unique permeation properties of α1E are maintained at the single-channel level, are independent of the nature of the expression system, and are not affected by coexpression of α2 and β subunits. Overall, the permeation characteristics of α1E are distinct from those described for R-type currents and share some similarities with native low-threshold Ca channels.Keywords
This publication has 46 references indexed in Scilit:
- Essential Ca 2+ -Binding Motif for Ca 2+ -Sensitive Inactivation of L-Type Ca 2+ ChannelsScience, 1995
- Expression of low-voltage activated Ca2+ channels from rat brain neurones in Xenopus oocytesNeuroReport, 1994
- Calcium currents recorded from a neuronal α1C L‐type calcium channel in Xenopus oocytesFEBS Letters, 1994
- Regulation of the cloned L‐type cardiac calcium channel by cyclic‐AMP‐dependent protein kinaseFEBS Letters, 1994
- Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neuronsNeuropharmacology, 1993
- Distinctive biophysical and pharmacological properties of class A (BI) calcium channel α1 subunitsNeuron, 1993
- Structure and Functional Expression of a Member of the Low Voltage-Activated Calcium Channel FamilyScience, 1993
- Structure and Functional Expression of an ω-Conotoxin-Sensitive Human N-Type Calcium ChannelScience, 1992
- Structure and functional expression of α1, α2, and β subunits of a novel human neuronal calcium channel subtypeNeuron, 1992
- Calcium currents in embryonic and neonatal mammalian skeletal muscle.The Journal of general physiology, 1988