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Functional compartmentalization of endosomal trafficking for the synaptic delivery of AMPA receptors during long-term potentiation.
Full Abstract
Endosomal membrane trafficking in dendritic spines is important for proper synaptic function and plasticity. However, little is known about the molecular identity and functional compartmentalization of the membrane trafficking machinery operating at the postsynaptic terminal. Here we report that the transport of AMPA-type glutamate receptors into synapses occurs in two discrete steps, and we identify the specific endosomal functions that control this process during long-term potentiation. We found that Rab11-dependent endosomes translocate AMPA receptors from the dendritic shaft into spines. Subsequently, an additional endosomal trafficking step, controlled by Rab8, drives receptor insertion into the synaptic membrane. Separate from this receptor delivery route, we show that Rab4 mediates a constitutive endosomal recycling within the spine. This Rab4-dependent cycling is critical for maintaining spine size but does not influence receptor transport. Therefore, our data reveal a highly compartmentalized endosomal network within the spine and identify the molecular components and functional organization of the membrane organelles that mediate AMPA receptor synaptic delivery during plasticity.
Author information
Author/s: Brown, Tyler C (TC); Correia, Susana S (SS); Petrok, Cortney N (CN); Esteban, José A (JA);
Affiliation: Neuroscience Program and Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Grants: F31-MH070205 (Agency:NIMH NIH HHS) ; MH070417 (Agency:NIMH NIH HHS)
Journal and publication information
Publication Type: In Vitro; Journal Article; Research Support, N.I.H., Extramural
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci), published in United States. (Language: eng)
Reference: 2007-Nov; vol 27 (issue 48) : pp 13311-5
Dates: Created 2007/11/29; Completed 2008/01/03;
PMID: 18045925, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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