Basal levels of AMPA receptor GluA1 subunit phosphorylation at threonine 840 and serine 845 in hippocampal neurons
- 1Department of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, California 90095, USA
- 2Interdepartmental Ph.D. Program for Neuroscience at UCLA, Los Angeles, California 90095, USA
- 3UCLA Integrative Center for Learning and Memory, Brain Research Institute, Los Angeles, California 90095, USA
- Corresponding author: todell{at}mednet.ucla.edu
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↵4 These authors contributed equally to this work.
Abstract
Dephosphorylation of AMPA receptor (AMPAR) GluA1 subunits at two sites, serine 845 (S845) and threonine 840 (T840), is thought to be involved in NMDA receptor-dependent forms of long-term depression (LTD). Importantly, the notion that dephosphorylation of these sites contributes to LTD assumes that a significant fraction of GluA1 subunits are basally phosphorylated at these sites. To examine this question, we used immunoprecipitation/depletion assays to estimate the proportion of GluA1 subunits basally phosphorylated at S845 and T840. Although dephosphorylation of S845 is thought to have a key role in LTD, our results indicate that few GluA1 subunits in hippocampal neurons are phosphorylated at this site. In contrast, ∼50% of GluA1 subunits are basally phosphorylated at T840, suggesting that dephosphorylation of this site can contribute to the down-regulation of AMPAR-mediated synaptic transmission in LTD.
Footnotes
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Article is online at http://www.learnmem.org/cgi/doi/10.1101/lm.040675.115.
- Received October 13, 2015.
- Accepted January 12, 2016.
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