Partners for adenosine A1 receptors

被引:0
|
作者
Rafael Franco
Francisco Ciruela
Vicent Casadó
Antonio Cortes
Enric I. Canela
Josefa Mallol
Luigi F. Agnati
Sergi Ferré
Kjell Fuxe
Carmen Lluis
机构
[1] University of Barcelona,Department of Biochemistry and Molecular Biology
[2] University of Modena,Department of Biomedical Sciences
[3] National Institute on Drug Abuse,Department of Health and Human Services
[4] Intramural Research Program,Department of Neuroscience
[5] NIH,undefined
[6] Karolinska Institutet,undefined
来源
关键词
Heteromer; dimer; G protein-coupled receptors; adenosine deaminase; glutamate; metabotroppic scaffold; caveolin; brain;
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摘要
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.
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页码:221 / 232
页数:11
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