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Publication : Transferrin Receptor Controls AMPA Receptor Trafficking Efficiency and Synaptic Plasticity.

First Author  Liu K Year  2016
Journal  Sci Rep Volume  6
Pages  21019 PubMed ID  26880306
Mgi Jnum  J:250166 Mgi Id  MGI:6102243
Doi  10.1038/srep21019 Citation  Liu K, et al. (2016) Transferrin Receptor Controls AMPA Receptor Trafficking Efficiency and Synaptic Plasticity. Sci Rep 6:21019
abstractText  Transferrin receptor (TFR) is an important iron transporter regulating iron homeostasis and has long been used as a marker for clathrin mediated endocytosis. However, little is known about its additional function other than iron transport in the development of central nervous system (CNS). Here we demonstrate that TFR functions as a regulator to control AMPA receptor trafficking efficiency and synaptic plasticity. The conditional knockout (KO) of TFR in neural progenitor cells causes mice to develop progressive epileptic seizure, and dramatically reduces basal synaptic transmission and long-term potentiation (LTP). We further demonstrate that TFR KO remarkably reduces the binding efficiency of GluR2 to AP2 and subsequently decreases AMPA receptor endocytosis and recycling. Thus, our study reveals that TFR functions as a novel regulator to control AMPA trafficking efficiency and synaptic plasticity.
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