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Mechanical Stimulation-induced Calcium Wave Propagation in Cell Monolayers: The Example of Bovine Corneal Endothelial Cells
Published on: July 16, 2013
The calcium channel α2/δ1 subunit interacts with ATP5b in the plasma membrane of developing muscle cells
1Dept. of Physiology and Biophysics, Univ. of Illinois at Chicago, 835 South Wolcott Ave., MC 901, Chicago, IL 60612, USA. garmar@uic.edu.
Insights
The α2/δ1 subunit interacts with ATP5b in developing muscle cells, independent of dihydropyridine receptors. This novel signaling complex influences calcium transient decay.
Area of Science:
- Muscle development
- Cellular signaling
- Biochemistry
Background:
- The α2/δ1 and α(1)1.1 subunits form the dihydropyridine receptor (DHPR) in adult skeletal muscle.
- During myotube development, α2/δ1 levels exceed α(1)1.1, suggesting roles beyond DHPRs.
Purpose of the Study:
- To identify binding partners of the α2/δ1 subunit during early myotube development when α(1)1.1 levels are low.
- To investigate the functional significance of novel α2/δ1 interactions.
Main Methods:
- Analysis of protein complexes in native configuration.
- Fluorescence resonance energy transfer (FRET).
- Coimmunoprecipitation assays.
Main Results:
- The α2/δ1 subunit associates with ATP5b, a subunit of mitochondrial ATP synthase.
- This interaction occurs in intracellular and plasma membranes, forming a functional signaling complex.
- The α2/δ1-ATP5b complex accelerates the decline of calcium transients, particularly under pulsed stimulation.
Conclusions:
- The α2/δ1 subunit has roles independent of DHPRs in developing myotubes.
- A novel signaling complex involving α2/δ1 and ATP5b at the plasma membrane modulates calcium dynamics.
Abstract:
The α2/δ1 and α(1)1.1 subunits are present at a 1:1 ratio in the dihydropyridine receptor (DHPR) from adult skeletal muscle. In contrast, during early myotube development α2/δ1 is present at higher levels than α(1)1.1 and localizes at the ends of the cells, suggesting that α2/δ1 may have a role independent from DHPRs. We sought to identify binding partners of α2/δ1 at a period when levels of α(1)1.1 are low. Analysis of protein complexes in their native configuration established that α2/δ1 may be associating with ATP5b, a subunit of a mitochondrial ATP synthase complex. This interaction was confirmed with fluorescence resonance energy transfer and coimmunoprecipitation. The association of α2/δ1 and ATP5b occurs in intracellular membranes and at the plasma membrane, where they form a functional signaling complex capable of accelerating the rate of decline of calcium transients. The acceleration of decay was more evident when myotubes were stimulated with a train of pulses. Our data indicate that the α2/δ1 subunit is not only part of the DHPR but that it may interact with other cellular components in developing myotubes, such as the ATP5b in its atypical localization in the plasma membrane.
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