Evidence map›Paper›PMID 27568566›Full record

ArticleCell reports2016

Upregulation of μ3A Drives Homeostatic Plasticity by Rerouting AMPAR into the Recycling Endosomal Pathway.

Celine C Steinmetz, Vedakumar Tatavarty, Ken Sugino, Yasuyuki Shima, Anne Joseph, Heather Lin, Michael Rutlin, Mary Lambo, Chris M Hempel, Benjamin W Okaty and 3 more

Abstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Activity Deprivation Modulates the Shank3/Homer1/mGluR5 Signaling Pathway to Enable Synaptic Upscaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. Modular arrangement of synaptic and intrinsic homeostatic plasticity within visual cortical circuits.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Postsynaptic receptors regulate presynaptic transmitter stability through transsynaptic bridges.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. MicroRNA-186-5p controls GluA2 surface expression and synaptic scaling in hippocampal neurons.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Review
  11. Article
  12. CaThe EMBO journal · 2018
    Article
  13. Recent Findings on AMPA Receptor Recycling.Frontiers in cellular neuroscience · 2018
    Review
  14. Article
  15. Mechanisms of AMPA Receptor Endosomal Sorting.Frontiers in molecular neuroscience · 2018
    Review
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Celine C SteinmetzDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Vedakumar TatavartyDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Ken SuginoDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Yasuyuki ShimaDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Anne JosephDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Heather LinDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Michael RutlinDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Mary LamboDepartment of Brain and Cognitive Science, MIT, Cambridge, MA 02139, USA.
Chris M HempelDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Benjamin W OkatyDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Suzanne ParadisDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA.
Sacha B NelsonDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA. Electronic address: nelson@brandeis.edu.
Gina G TurrigianoDepartment of Biology and Center for Behavioral Genomics, Brandeis University, Waltham, MA 02454, USA. Electronic address: turrigiano@brandeis.edu.

Funding

Quantitative Neuroscience: Tools for Bridging Levels of AnalysisT32NS007292 · NINDS · BRANDEIS UNIVERSITY · PI GINA G TURRIGIANO · 1986 to 2026
$12.7M
SETTING FIRING RATE SET POINTS IN NEOCORTICAL PYRAMIDAL NEURONSP01NS079419 · NINDS · BRANDEIS UNIVERSITY · PI TURRIGIANO, GINA G · 2013 to 2017
$6.2M
Semaphorin-Dependent GABAergic Synapse Formation: A Novel Approach to Increasing Inhibition in the Intact BrainR01NS065856 · NINDS · BRANDEIS UNIVERSITY · PI PARADIS, SUZANNE · 2010 to 2024
$5.4M
A genetic and genomic resource for vision researchR01EY022360 · NEI · BRANDEIS UNIVERSITY · PI NELSON, SACHA B · 2012 to 2016
$2.0M
Synaptic Homeostasis in Neocortical Neurons and CircuitsR37NS092635 · NINDS · BRANDEIS UNIVERSITY · PI TURRIGIANO, GINA G · 2015 to 2018
$1.6M
Zeiss Axioimager Z2 Imaging System for Array TomographyS10RR031531 · NCRR · BRANDEIS UNIVERSITY · PI NELSON, SACHA B · 2011 to 2011
$156k
NCRR NIH HHS S10 RR031531NEI NIH HHS R01 EY022360NINDS NIH HHS P01 NS079419NINDS NIH HHS R01 NS065856NINDS NIH HHS R37 NS092635NINDS NIH HHS T32 NS007292
6 · The paper itself

Abstract

Synaptic scaling is a form of homeostatic plasticity driven by transcription-dependent changes in AMPA-type glutamate receptor (AMPAR) trafficking. To uncover the pathways involved, we performed a cell-type-specific screen for transcripts persistently altered during scaling, which identified the μ subunit (μ3A) of the adaptor protein complex AP-3A. Synaptic scaling increased μ3A (but not other AP-3 subunits) in pyramidal neurons and redistributed dendritic μ3A and AMPAR to recycling endosomes (REs). Knockdown of μ3A prevented synaptic scaling and this redistribution, while overexpression (OE) of full-length μ3A or a truncated μ3A that cannot interact with the AP-3A complex was sufficient to drive AMPAR to REs. Finally, OE of μ3A acted synergistically with GRIP1 to recruit AMPAR to the dendritic membrane. These data suggest that excess μ3A acts independently of the AP-3A complex to reroute AMPAR to RE, generating a reservoir of receptors essential for the regulated recruitment to the synaptic membrane during scaling up.

Indexed as

HomeostasisUp-RegulationAdaptor Protein Complex 3Adaptor Protein Complex mu SubunitsAdaptor Proteins, Signal TransducingAnimalsDendritesDiscs Large Homolog 1 ProteinEndocytosisEndosomesGene Knockdown TechniquesMiceNerve Tissue ProteinsNeuronal PlasticityPyramidal CellsReceptors, AMPAAdaptor Protein Complex 3Adaptor Protein Complex mu SubunitsAdaptor Proteins, Signal TransducingDiscs Large Homolog 1 ProteinDlg1 protein, mouseglutamate receptor ionotropic, AMPA 2Grip1 protein, mouseNerve Tissue ProteinsReceptors, AMPA

Identifiers

PMID27568566
PMCPMC5226429

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.