Sergé Arnauld, Fourgeaud Lawrence, Hémar Agnès, Choquet Daniel
Physiologie Cellulaire de la Synapse, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5091, Institut François Magendie, 33077 Bordeaux, France.
J Neurosci. 2002 May 15;22(10):3910-20. doi: 10.1523/JNEUROSCI.22-10-03910.2002.
Glutamate receptors are clustered at the membrane through interactions with intracellular scaffolding proteins and cytoskeletal elements but can also be found in intracellular compartments or dispersed in the membrane. This distribution results from an equilibrium between the different pools of receptors whose dynamic is poorly known. The group I metabotropic glutamate receptor 5 (mGluR5) is concentrated in an annulus around the postsynaptic density but also found in large amounts in the extrasynaptic membrane. To analyze the dynamic of stabilization of mGluR5, we used single-particle tracking, force measurements, and fluorescence recovery to measure the mobility of mGluR5. We found that receptor activation increases receptor diffusion, whereas the scaffolding protein Homer favors confinement of receptor movements within clusters of Homer-mGluR5. However, this stabilization is reversible, because even in the presence of Homer, receptors still enter and exit from clusters at fast rates. Furthermore, clusters themselves are highly dynamic both in their movements and in their composition, which can vary within tens of seconds. Thus, exchange of receptors between dispersed and clustered states is fast and regulated during physiological processes. These properties may explain certain fast changes in receptor composition observed at postsynaptic densities.
谷氨酸受体通过与细胞内支架蛋白和细胞骨架成分相互作用而聚集在细胞膜上,但也可存在于细胞内区室或分散在细胞膜中。这种分布是由不同受体池之间的平衡导致的,而其动态变化鲜为人知。I 型代谢型谷氨酸受体 5(mGluR5)集中在突触后致密区周围的环状区域,但在突触外膜中也大量存在。为了分析 mGluR5 稳定化的动态过程,我们使用单粒子追踪、力测量和荧光恢复来测量 mGluR5 的流动性。我们发现受体激活会增加受体扩散,而支架蛋白 Homer 则有利于将受体运动限制在 Homer-mGluR5 簇内。然而,这种稳定化是可逆的,因为即使在有 Homer 的情况下,受体仍以快速速率进出簇。此外,簇本身在其运动和组成方面都具有高度动态性,其组成可在数十秒内发生变化。因此,在生理过程中,受体在分散状态和聚集状态之间的交换快速且受到调控。这些特性可能解释了在突触后致密区观察到的受体组成的某些快速变化。