Evidence map›Paper›PMID 23479744›Full record

ArticleThe Journal of cell biology2013

Bidirectional Ca²⁺ signaling occurs between the endoplasmic reticulum and acidic organelles.

Anthony J Morgan, Lianne C Davis, Siegfried K T Y Wagner, Alexander M Lewis, John Parrington, Grant C Churchill, Antony Galione

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
16.4field-weighted citation impact, top 1% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. Stay in touch with the endoplasmic reticulum.Science China. Life sciences · 2024
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Endolysosomal TPCs regulate social behavior by controlling oxytocin secretion.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. TRPML1-Induced Lysosomal CaInternational journal of molecular sciences · 2023
    Article
  8. NAADP-Mediated CaHandbook of experimental pharmacology · 2023
    Article
  9. GABACells · 2022
    Article
  10. Two-pore channels: going with the flows.Biochemical Society transactions · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. The lysosomotrope GPN mobilises CaJournal of cell science · 2021
    Article
  20. IPProgress in molecular and subcellular biology · 2021
    Review

16 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

7 authors at 1 institution in 1 country.

Anthony J MorganDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, England, UK. antony.galione@pharm.ox.ac.uk
Lianne C Davis
Siegfried K T Y Wagner
Alexander M Lewis
John Parrington
Grant C Churchill
Antony Galione
University of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G008523/1Wellcome Trust
6 · The paper itself

Abstract

The endoplasmic reticulum (ER) and acidic organelles (endo-lysosomes) act as separate Ca(2+) stores that release Ca(2+) in response to the second messengers IP3 and cADPR (ER) or NAADP (acidic organelles). Typically, trigger Ca(2+) released from acidic organelles by NAADP subsequently recruits IP3 or ryanodine receptors on the ER, an anterograde signal important for amplification and Ca(2+) oscillations/waves. We therefore investigated whether the ER can signal back to acidic organelles, using organelle pH as a reporter of NAADP action. We show that Ca(2+) released from the ER can activate the NAADP pathway in two ways: first, by stimulating Ca(2+)-dependent NAADP synthesis; second, by activating NAADP-regulated channels. Moreover, the differential effects of EGTA and BAPTA (slow and fast Ca(2+) chelators, respectively) suggest that the acidic organelles are preferentially activated by local microdomains of high Ca(2+) at junctions between the ER and acidic organelles. Bidirectional organelle communication may have wider implications for endo-lysosomal function as well as the generation of Ca(2+) oscillations and waves.

Indexed as

AnimalsCalciumCalcium SignalingChelating AgentsEgtazic AcidEndoplasmic ReticulumEndosomesLysosomesLytechinusNADP1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acidCalciumChelating AgentsEgtazic AcidNAADPNADP

Identifiers

PMID23479744
PMCPMC3601362
OpenAlexW1983181941

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.