Overexpression of CaV beta subunits increased basal current density and decreased the magnitude of PKA regulation, revealing a limited functional reserve for PKA modulation of CaV1.2 channels.
Does overexpression of specific CaV beta subunits alter PKA modulation of cardiac CaV1.2 channels in heart cells?
The study redefines the role of beta subunits in PKA modulation of CaV1.2 channels, demonstrating that beta phosphorylation is not necessary and revealing a limited functional reserve for this regulation in the heart.
Protein kinase A (PKA)-mediated enhancement of L-type calcium currents (I(Ca,L)) is essential for sympathetic regulation of the heartbeat and is the classic example of channel regulation by phosphorylation, and its loss is a common hallmark of heart failure. Mechanistic understanding of how distinct Ca(V) channel subunits contribute to PKA modulation of I(Ca,L) has been intensely pursued yet remains elusive. Moreover, critical features of this regulation such as its functional reserve (the surplus capacity available for modulation) in the heart are unknown. Here, we use an overexpression paradigm in heart cells to simultaneously identify the impact of auxiliary Ca(V)betas on PKA modulation of I(Ca,L) and to gauge the functional reserve of this regulation in the heart. Ca(V)1.2 channels containing wild-type beta(2a) or a phosphorylation-deficient mutant (beta(2a,AAA)) were equally upregulated by PKA, discounting a necessary role for beta phosphorylation. Nevertheless, channels reconstituted with beta(2a) displayed a significantly diminished PKA response compared with other beta isoforms, an effect explainable by a uniquely higher basal P(o) of beta(2a) channels. Overexpression of all betas increased basal current density, accompanied by a concomitant decrease in the magnitude of PKA regulation. Scatter plots of fold increase in current against basal current density revealed an inverse relationship that was conserved across species and conformed to a model in which a large fraction of channels remained unmodified after PKA activation. These results redefine the role of beta subunits in PKA modulation of Ca(V)1.2 channels and uncover a new design principle of this phenomenon in the heart, vis à vis a limited functional reserve.
Miriyala et al. (Fri,) reported a other. Overexpression of auxiliary CaV beta subunits vs. Other beta isoforms or basal state was evaluated on PKA modulation of L-type calcium currents (I(Ca,L)). Overexpression of CaV beta subunits increased basal current density and decreased the magnitude of PKA regulation, revealing a limited functional reserve for PKA modulation of CaV1.2 channels.