Evidence map›Paper›PMID 23864710›Full record

ArticleMolecular biology of the cell2013

Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs.

Philip D Fox, Christopher J Haberkorn, Aubrey V Weigel, Jenny L Higgins, Elizabeth J Akin, Matthew J Kennedy, Diego Krapf, Michael M Tamkun

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Pentameric assembly of the Kv2.1 tetramerization domain.Acta crystallographica. Section D, Structural biology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Lipid transporter TMEM24/C2CD2L is a CaProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. Review
  12. Kv2 potassium channels form endoplasmic reticulum/plasma membrane junctions via interaction with VAPA and VAPB.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. ER-plasma membrane junctions: Why and how do we study them?Biochimica et biophysica acta. Molecular cell research · 2017
    Review
  17. Article
  18. Disruption of KNeuroscience · 2017
    Article
  19. STIM1 CaCell reports · 2017
    Article
  20. 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

8 authors at 2 institutions in 1 country.

Philip D FoxDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Christopher J Haberkorn
Aubrey V Weigel
Jenny L Higgins
Elizabeth J Akin
Matthew J Kennedy
Diego Krapf
Michael M Tamkun
Colorado State University · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Mechanisms of dendritic exocytosisR01NS082271 · NINDS · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2013 to 2017
$1.7M
Kv2.1 membrane corrals:Regulators of K+ channel function and traffickingR01GM084136 · NIGMS · COLORADO STATE UNIVERSITY · PI TAMKUN, MICHAEL M. · 2009 to 2012
$1.6M
NIGMS NIH HHS R01 GM084136NIGMS NIH HHS R01GM084136S1NIGMS NIH HHS R01GM84136NINDS NIH HHS R01 NS082271
6 · The paper itself

Abstract

In mammalian cells, the cortical endoplasmic reticulum (cER) is a network of tubules and cisterns that lie in close apposition to the plasma membrane (PM). We provide evidence that PM domains enriched in underlying cER function as trafficking hubs for insertion and removal of PM proteins in HEK 293 cells. By simultaneously visualizing cER and various transmembrane protein cargoes with total internal reflectance fluorescence microscopy, we demonstrate that the majority of exocytotic delivery events for a recycled membrane protein or for a membrane protein being delivered to the PM for the first time occur at regions enriched in cER. Likewise, we observed recurring clathrin clusters and functional endocytosis of PM proteins preferentially at the cER-enriched regions. Thus the cER network serves to organize the molecular machinery for both insertion and removal of cell surface proteins, highlighting a novel role for these unique cellular microdomains in membrane trafficking.

Indexed as

Protein TransportCell MembraneCell MovementClathrinEndocytosisEndoplasmic ReticulumExocytosisHEK293 CellsHumansKv1.4 Potassium ChannelMembrane ProteinsMicroscopy, FluorescenceReceptors, TransferrinShab Potassium ChannelsClathrinKCNB1 protein, humanKv1.4 Potassium ChannelMembrane ProteinsReceptors, TransferrinShab Potassium Channels

Identifiers

PMID23864710
PMCPMC3756922
OpenAlexW2154990586

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.