| Literature DB >> 1648939 |
P S McPherson1, Y K Kim, H Valdivia, C M Knudson, H Takekura, C Franzini-Armstrong, R Coronado, K P Campbell.
Abstract
The release of stored Ca2+ from intracellular pools triggers a variety of important neuronal processes. Physiological and pharmacological evidence has indicated the presence of caffeine-sensitive intracellular pools that are distinct from the well-characterized inositol 1,4,5,-trisphosphate (IP3)-gated pools. Here we report that the brain ryanodine receptor functions as a caffeine- and ryanodine-sensitive Ca2+ release channel that is distinct from the brain IP3 receptor. The brain ryanodine receptor has been purified 6700-fold with no change in [3H]ryanodine binding affinity and shown to be a homotetramer composed of an approximately 500 kd protein subunit, which is identified by anti-peptide antibodies against the skeletal and cardiac muscle ryanodine receptors. Our results demonstrate that the brain ryanodine receptor functions as a caffeine-sensitive Ca2+ release channel and thus is the likely gating mechanism for intracellular caffeine-sensitive Ca2+ pools in neurons.Entities:
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Year: 1991 PMID: 1648939 DOI: 10.1016/0896-6273(91)90070-g
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173