| Literature DB >> 16012195 |
Rafael Franco1, Francisco Ciruela, Vicent Casadó, Antonio Cortes, Enric I Canela, Josefa Mallol, Luigi F Agnati, Sergi Ferré, Kjell Fuxe, Carmen Lluis.
Abstract
G protein-coupled receptors (GPCRs) are targets for therapy in a variety of neurological diseases. Using adenosine A1 receptors (A1Rs) as paradigm of GPCRs, this review focuses on how protein-protein interactions, from monomers to heteromers, can contribute to hormone/neurotransmitter/neuromodulator regulation. The interaction of A1Rs with other membrane receptors, enzymes, and adaptor and scaffolding proteins is relevant for receptor traffic, internalization, and desensitization, and A1Rs are extremely important in driving signaling through different intracellular pathways. There is even the possibility of linking together GPCR heteromeric complexes with ion channel receptors in a receptor mosaic that might have special integrative value and might constitute the molecular basis for learning and memory.Entities:
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Year: 2005 PMID: 16012195 DOI: 10.1385/JMN:26:2-3:221
Source DB: PubMed Journal: J Mol Neurosci ISSN: 0895-8696 Impact factor: 3.444