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Abstract Long-term depression (LTD) of synaptic strength can take multiple forms and contribute to circuit remodeling, memory encoding or erasure. The generic term LTD encompasses various induction pathways, including activation of NMDA, mGlu or P2X receptors. However, the associated specific molecular mechanisms and effects on synaptic physiology are still unclear. We here compare how NMDAR- or P2XR-dependent LTD affect synaptic nanoscale organization and function in rodents. While both LTDs are associated with a loss and reorganization of synaptic AMPARs, only NMDAR-dependent LTD induction triggers a profound reorganization of PSD-95. This modification, which requires the autophagy machinery to remove the T19-phosphorylatedmore »Free, publicly-accessible full text available December 1, 2022
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Jullié, Damien ; Stoeber, Miriam ; Sibarita, Jean-Baptiste ; Zieger, Hanna L. ; Bartol, Thomas M. ; Arttamangkul, Seksiri ; Sejnowski, Terrence J. ; Hosy, Eric ; von Zastrow, Mark ( , Neuron)