Receptor-receptor interactions: A novel concept in brain integration

被引:54
作者
Agnati, Luigi F. [1 ,2 ]
Guidolin, Diego [3 ]
Leo, Giuseppina [1 ,2 ]
Carone, Chiara [1 ,2 ]
Genedani, Susanna [1 ,2 ]
Fuxe, Kjell [4 ]
机构
[1] Univ Modena, Dept Biomed Sci, Lido Venezia, Italy
[2] IRCCS San Camillo, Lido Venezia, Italy
[3] Univ Padua, Dept Human Anat & Physiol, Padua, Italy
[4] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
关键词
Receptor mosaic; Atomic Force Microscopy; Parkinson's Disease; Homocysteine; Allosterism; CENTRAL-NERVOUS-SYSTEM; PROTEIN-COUPLED RECEPTORS; LONG-TERM POTENTIATION; VOLUME TRANSMISSION; DOPAMINE-D-2; RECEPTORS; ALLOSTERIC MODULATION; MOLECULAR NETWORKS; PARKINSONS-DISEASE; MOSAIC HYPOTHESIS; NEUROPEPTIDE-Y;
D O I
10.1016/j.pneurobio.2009.10.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A brief historical presentation of the hypothesis on receptor-receptor interactions as an important integrative mechanism taking place at plasma membrane level is given. Some concepts derived from this integrative mechanism especially the possible assemblage of receptors in receptor mosaics (high-order receptor oligomers) and their relevance for the molecular networks associated with the plasma membrane are discussed. In particular, the Rodbell's disaggregation theory for G-proteins is revisited in the frame of receptor mosaic model. The paper also presents some new indirect evidence on A2A boolean AND D2 receptor interactions obtained by means of Atomic Force Microscopy on immunogold preparations of A2A and D2 receptors in CHO cells. These findings support previous data obtained by means of computer-assisted confocal laser microscopy. The allosteric control of G-protein coupled receptors is examined in the light of the new views on allosterism and recent data on a homocysteine analogue capable of modulating D2 receptors are shown. Finally, the hypothesis is introduced on the existence of check-points along the amino acid pathways connecting allosteric and orthosteric binding sites of a receptor and their potential importance for drug development. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:157 / 175
页数:19
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