Evidence map›Paper›PMID 19765991›Full record

ArticleCurrent biology : CB2009

Ribosome-free terminals of rough ER allow formation of STIM1 puncta and segregation of STIM1 from IP(3) receptors.

Gyorgy Lur, Lee P Haynes, Ian A Prior, Oleg V Gerasimenko, Stefan Feske, Ole H Petersen, Robert D Burgoyne, Alexei V Tepikin

Open access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

63 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The role of CaCell calcium · 2023
    Review
  7. Review
  8. Article
  9. Intracellular CaInternational journal of molecular sciences · 2020
    Review
  10. Review
  11. Article
  12. Review
  13. The Orai CaThe Journal of physiology · 2019
    Article
  14. Mitochondrial junctions with cellular organelles: CaPflugers Archiv : European journal of physiology · 2018
    Review
  15. Can pancreatitis be treated by inhibiting CaAnnals of translational medicine · 2018
    Article
  16. Article
  17. CaOncotarget · 2017
    Review
  18. CaNature communications · 2017
    Article
  19. ER-plasma membrane junctions: Why and how do we study them?Biochimica et biophysica acta. Molecular cell research · 2017
    Review
  20. CaThe Journal of physiology · 2017
    Review

3 more citing papers are in PubMed but not listed here.

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 2 countries.

Gyorgy LurDepartment of Physiology, School of Biomedical Sciences, University of Liverpool, Liverpool L69 3BX, UK.
Lee P Haynes
Ian A Prior
Oleg V Gerasimenko
Stefan Feske
Ole H Petersen
Robert D Burgoyne
Alexei V Tepikin
University of Liverpool · GBNYU Langone Health · US

Funding

Medical Research Council G0700167Medical Research Council G9900432Wellcome Trust 074766Wellcome Trust 080906/Z/06/ZWellcome Trust 082151
6 · The paper itself

Abstract

Store-operated Ca(2+) entry is a ubiquitous mechanism that prevents the depletion of endoplasmic reticulum (ER) calcium. A reduction of ER calcium triggers translocation of STIM proteins, which serve as calcium sensors in the ER, to subplasmalemmal puncta where they interact with and activate Orai channels. In pancreatic acinar cells, inositol 1,4,5-trisphosphate (IP(3)) receptors populate the apical part of the ER. Here, however, we observe that STIM1 translocates exclusively to the lateral and basal regions following ER Ca(2+) loss. This finding is paradoxical because the basal and lateral regions of the acinar cells contain rough ER (RER); the size of the ribosomes that decorate RER is larger than the distance that can be spanned by a STIM-Orai complex, and STIM1 function should therefore not be possible. We resolve this paradox and characterize ribosome-free terminals of the RER that form junctions between the reticulum and the plasma membrane in the basal and lateral regions of the acinar cells. Our findings indicate that different ER compartments specialize in different calcium-handling functions (Ca(2+) release and Ca(2+) reloading) and that any potential interference between Ca(2+) release and Ca(2+) influx is minimized by the spatial separation of the two processes.

Indexed as

AnimalsCalciumCalcium ChannelsEndoplasmic ReticulumInositol 1,4,5-Trisphosphate ReceptorsMembrane GlycoproteinsMiceMicroscopy, ConfocalMicroscopy, ElectronPancreasPlasmidsProtein TransportRibosomesStromal Interaction Molecule 1CalciumCalcium ChannelsInositol 1,4,5-Trisphosphate ReceptorsMembrane GlycoproteinsStim1 protein, mouseStromal Interaction Molecule 1

Identifiers

PMID19765991
PMCPMC2887489
OpenAlexW2168026341

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.