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Stargazing regulates synaptic targeting of AMPA receptors by two distinct mechanisms.

机译:观星通过两种不同的机制调节AMPA受体的突触靶向。

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摘要

Stargazer, an ataxic and epileptic mutant mouse, lacks functional AMPA (alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate) receptors on cerebellar granule cells. Stargazin, the mutated protein, interacts with both AMPA receptor subunits and synaptic PDZ proteins, such as PSD-95. The interaction of stargazin with AMPA receptor subunits is essential for delivering functional receptors to the surface membrane of granule cells, whereas its binding with PSD-95 and related PDZ proteins through a carboxy-terminal PDZ-binding domain is required for targeting the AMPA receptor to synapses. Expression of a mutant stargazin lacking the PDZ-binding domain in hippocampal pyramidal cells disrupts synaptic AMPA receptors, indicating that stargazin-like mechanisms for targeting AMPA receptors may be widespread in the central nervous system.
机译:Stargazer是一种共济失调和癫痫突变小鼠,在小脑颗粒细胞上缺乏功能性AMPA(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯)受体。突变蛋白Stargazin与AMPA受体亚基和突触PDZ蛋白(例如PSD-95)相互作用。 Stargazin与AMPA受体亚基的相互作用对于将功能性受体传递至颗粒细胞的表面膜至关重要,而将其通过羧基端PDZ结合域与PSD-95和相关PDZ蛋白结合需要将AMPA受体靶向到突触。在海马锥体细胞中缺乏PDZ结合结构域的突变stargazin的表达破坏了突触AMPA受体,表明靶向AMPA受体的stargazin样机制可能在中枢神经系统中广泛分布。

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