Article ID Journal Published Year Pages File Type
4330883 Brain Research 2007 11 Pages PDF
Abstract

Voltage-dependent calcium channels are important for calcium influx and the ensuing intracellular calcium signal in various excitable membranes. The β subunits of these channels modify calcium currents through pore-forming α1 subunits of the high-voltage- activated calcium channels. In the present study, β3 subunit-null mice were used to investigate the importance of the β3 subunit of the voltage-dependent calcium channel, which couples with the CaV2.2 (α1B) subunit to form the major component of neuronal N-type calcium channels in the brain. Western blot analysis revealed a significant decrease in N-type calcium channels in β3 subunit-null mice, while protein levels of other high-voltage-activated calcium channel α1 subunits were unchanged. Immunoprecipitation analysis with an anti-CaV2.2 antibody showed that reshuffling of the assembly of N-type channels had occurred in the β3 subunit-null mice. Ablation of this subunit resulted in modified nociception, decreased anxiety, and increased aggression. The β3 subunit-null mice also showed impaired learning ability. These results suggest the importance of voltage-dependent calcium channels and the key role of the β3 subunit in memory formation, nociceptive sensory transduction, and various neurological signal transduction pathways.

Related Topics
Life Sciences Neuroscience Neuroscience (General)
Authors
, , , , , , ,