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Research Papers
Auxiliary β Subunits Differentially Determine PKA Utilization of Distinct Regulatory Sites on CaV1.3 L-Type Ca2+ Channels
Yixin Liang and Steven J. Tavalin
volume 1 | issue 2
March/April 2007Pages: 102 - 112
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L-type calcium channels (CaV1.1–CaV1.4) link Ca2+ influx to membrane depolarization and serve a critical role in regulating membrane excitability, muscle contraction, hormone secretion, and gene transcription. In many tissues, L-type calcium channel activity (CaV1.1 and CaV1.2) is enhanced by transmitters and hormones that activate the cAMP-dependent protein kinase (PKA), which is largely thought to be mediated via phosphorylation of the pore forming α subunit. However, the ability of PKA to regulate CaV1.3 and the sites contributing to effective modulation of channel activity remains to be established. Using HEK 293 cells, we demonstrate that currents carried by the long C-terminal splice variant of CaV1.3 (CaV1.3L) are selectively enhanced compared to the short C-terminal splice variant (CaV1.3S) when the catalytic subunit of PKA is introduced into the cell via the whole-cell recording electrode. However, the persistence of this regulation is dependent on the identity of the auxiliary β subunit, such that PKA produces only a transient increase in the presence of β3 while a persistent increase is observed in the presence of the β2a subunit. Site-directed mutagenesis of consensus PKA phosphorylation sites revealed that Ser1964 and Ser1743 in CaV1.3L were the predominant sites controlling PKA modulation in the presence of the β3 and β2a auxiliary subunits, respectively. Therefore, β subunits determine the contribution of distinct sites within CaV1.3 towards PKA-mediated enhancement of channel activity. These data suggest that auxiliary β subunits govern the access of signaling enzymes to L-type calcium channels.
Authors
Yixin Liang
Department of Pharmacology, University of Tennessee Health Science Center, Memphis, TN
Steven J. Tavalin
Department of Pharmacology, University of Tennessee Health Science Center, Memphis, TN
We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:
Download PDF If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.