Reconstitution of β-adrenergic regulation of CaV1.2: Rad-dependent and Rad-independent protein kinase A mechanisms

Proc Natl Acad Sci U S A. 2021 May 25;118(21):e2100021118. doi: 10.1073/pnas.2100021118.

Abstract

L-type voltage-gated CaV1.2 channels crucially regulate cardiac muscle contraction. Activation of β-adrenergic receptors (β-AR) augments contraction via protein kinase A (PKA)-induced increase of calcium influx through CaV1.2 channels. To date, the full β-AR cascade has never been heterologously reconstituted. A recent study identified Rad, a CaV1.2 inhibitory protein, as essential for PKA regulation of CaV1.2. We corroborated this finding and reconstituted the complete pathway with agonist activation of β1-AR or β2-AR in Xenopus oocytes. We found, and distinguished between, two distinct pathways of PKA modulation of CaV1.2: Rad dependent (∼80% of total) and Rad independent. The reconstituted system reproduces the known features of β-AR regulation in cardiomyocytes and reveals several aspects: the differential regulation of posttranslationally modified CaV1.2 variants and the distinct features of β1-AR versus β2-AR activity. This system allows for the addressing of central unresolved issues in the β-AR-CaV1.2 cascade and will facilitate the development of therapies for catecholamine-induced cardiac pathologies.

Keywords: adrenergic; calcium channel; cardiac; heterologous; protein kinase A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Channels, L-Type / genetics
  • Calcium Channels, L-Type / metabolism*
  • Cyclic AMP / metabolism
  • Cyclic AMP-Dependent Protein Kinases / genetics
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Gene Expression Regulation
  • Humans
  • Ion Transport
  • Mice
  • Mutation
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / metabolism*
  • Oocytes / cytology
  • Oocytes / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA / genetics
  • RNA / metabolism
  • Rabbits
  • Receptors, Adrenergic, beta / genetics
  • Receptors, Adrenergic, beta / metabolism*
  • Xenopus laevis
  • ras Proteins / genetics
  • ras Proteins / metabolism*

Substances

  • Calcium Channels, L-Type
  • L-type calcium channel alpha(1C)
  • Protein Isoforms
  • RRAD protein, human
  • Receptors, Adrenergic, beta
  • RNA
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • ras Proteins
  • Calcium