Heptaspanning membrane receptors and cytoskeletal/scaffolding proteins -: Focus on adenosine, dopamine, and metabotropic glutamate receptor function

被引:22
作者
Ciruela, F [1 ]
Canela, L
Burgueño, J
Soriguera, A
Cabello, N
Canela, EI
Casadó, V
Cortés, A
Mallol, J
Woods, AS
Ferré, S
Lluis, C
Franco, R
机构
[1] Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
[2] Target Validat, Lab Dr Esteve, Barcelona 08028, Spain
[3] NIDA, Behav Neurosci Branch, Intramural Res Program, NIH,Dept Hlth & Human Serv, Baltimore, MD 21224 USA
关键词
GPCR; adenosine; glutamate; dopamine; protein-protein interaction;
D O I
10.1385/JMN:26:2-3:277
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most cellular functions are mediated by multiprotein complexes. In neurons, these complexes are directly involved in the proper neuronal transmission, which is responsible for phenomena like learning, memory and development. In recent years studies based on two-hybrid screens and proteomic, biochemical, and cell biology approaches have shown that intracellular domains of G protein-coupled receptors (GPCRs) or heptaspanning membrane receptors (HSMRs) interact with intracellular proteins. These interactions are the basis of a protein network associated with these receptors, which includes scaffolding proteins containing one or several PDZ (post-synaptic-density-95 /discs-large/zona occludens-1) domains, signaling proteins, and proteins of the cytoskeleton. The present article is focused on the emerging evidence for interactions of adenosine, dopamine, and metabotropic glutamate receptors, with scaffolding and cytoskeletal proteins that play a role in the targeting and anchoring of these receptors to the plasma membrane, thus contributing to neuronal development and plasticity. Finally, given the complexity of neurological disorders such as ischemic stroke, Alzheimer's disease, and epilepsy, exploitation of these HSMR-associated interactions might prove to be efficient in the treatment of such disorders.
引用
收藏
页码:277 / 292
页数:16
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