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Disruption of AMPA receptor GluR2 clusters following long-term depression induction in cerebellar Purkinje neurons

机译:小脑浦肯野神经元长期抑郁诱导后AMPA受体GluR2簇的破坏

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摘要

Cerebellar long-term depression (LTD) is thought to play an important role in certain types of motor learning. However, the molecular mechanisms underlying this event have not been clarified. Here, using cultured Purkinje cells, we show that stimulations inducing cerebellar LTD cause phosphorylation of Ser880 in the intracellular C-terminal domain of the AMPA receptor subunit GluR2. This phosphorylation is accompanied by both a reduction in the affinity of GluR2 to glutamate receptor interacting protein (GRIP), a molecule known to be critical for AMPA receptor clustering, and a significant disruption of postsynaptic GluR2 clusters. Moreover, GluR2 protein released from GRIP is shown to be internalized. These results suggest that the dissociation of postsynaptic GluR2 clusters and subsequent internalization of the receptor protein, initiated by the phosphorylation of Ser880, are the mechanisms underlying the induction of cerebellar LTD.
机译:小脑长期抑郁症(LTD)被认为在某些类型的运动学习中起着重要作用。但是,尚不清楚该事件的潜在分子机制。在这里,使用培养的浦肯野细胞,我们显示刺激诱导小脑LTD引起AMPA受体亚基GluR2的细胞内C末端域中Ser880的磷酸化。这种磷酸化伴随着GluR2对谷氨酸受体相互作用蛋白(GRIP)的亲和力降低(已知对AMPA受体簇至关重要的分子)以及突触后GluR2簇的显着破坏。而且,从GRIP释放的GluR2蛋白显示为被内在化。这些结果表明,由Ser880的磷酸化引发的突触后GluR2簇的解离和随后受体蛋白的内在化是诱导小脑LTD的基础机制。

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