Abstract
Calcium influx into any cell requires fine tuning to guarantee the correct balance between activation of calcium-dependent processes, such as muscle contraction and neurotransmitter release, and calcium-induced cell damage. G protein-coupled receptors play a critical role in negative feedback to modulate the activity of the CaV2 subfamily of the voltage-dependent calcium channels, which are largely situated on neuronal and neuro-endocrine cells. The basis for the specificity of the relationships among membrane receptors, G proteins, and effector calcium channels will be discussed, as well as the mechanism by which G protein-mediated inhibition is thought to occur. The inhibition requires free Gβγ dimers, and the cytoplasmic linker between domains I and II of the CaV2 α1 subunits binds Gβγ dimers, whereas the intracellular N terminus of CaV2 α1 subunits provides essential determinants for G protein modulation. Evidence suggests a key role for the β subunits of calcium channels in the process of G protein modulation, and the role of a class of proteins termed “regulators of G protein signaling” will also be described.
- The American Society for Pharmacology and Experimental Therapeutics
PharmRev articles become freely available 12 months after publication, and remain freely available for 5 years.Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page.
|