Evidence map›Paper›PMID 26924250›Full record

ReviewBiochimica et biophysica acta2016

Homeostatic regulation of the PI(4,5)P2-Ca(2+) signaling system at ER-PM junctions.

Chi-Lun Chang, Jen Liou

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Roles of Cholesterol and PtdIns(4,5)PAdvances in experimental medicine and biology · 2023
    Review
  12. Article
  13. Article
  14. Phosphoinositide transport and metabolism at membrane contact sites.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Review
  15. Review
  16. PIPCell calcium · 2021
    Article
  17. SLC6 transporter oligomerization.Journal of neurochemistry · 2021
    Review
  18. ER-PM Contact Sites - SNARING Actors in Emerging Functions.Frontiers in cell and developmental biology · 2021
    Review
  19. Rushing to maintain plasma membrane phosphoinositide levels.The Journal of general physiology · 2020
    Article
  20. Store-Operated Calcium Channels: From Function to Structure and Back Again.Cold Spring Harbor perspectives in biology · 2020
    Review
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

2 authors at 1 institution in 1 country.

Chi-Lun ChangDepartment of Physiology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Jen LiouDepartment of Physiology, UT Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: Jen.Liou@UTSouthwestern.edu.
Southwestern Medical Center · US

Funding

Functions and regulation of endoplasmic reticulum-plasma membrane junctionsR01GM113079 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI LIOU, JEN · 2016 to 2020
$1.6M
NIGMS NIH HHS GM113079NIGMS NIH HHS R01 GM113079
6 · The paper itself

Abstract

The phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2)-Ca(2+) signaling system is important for cell activation in response to various extracellular stimuli. This signaling system is initiated by receptor-induced hydrolysis of PI(4,5)P2 in the plasma membrane (PM) to generate the soluble second messenger inositol 1,4,5-trisphosphate (IP3). IP3 subsequently triggers the release of Ca(2+) from the endoplasmic reticulum (ER) store to the cytosol to activate Ca(2+)-mediated responses, such as secretion and proliferation. The consumed PM PI(4,5)P2 and ER Ca(2+) must be quickly restored to sustain signaling responses, and to maintain the homeostasis of PI(4,5)P2 and Ca(2+). Since phosphatidylinositol (PI), the precursor lipid for PM PI(4,5)P2, is synthesized in the ER membrane, and a Ca(2+) influx across the PM is required to refill the ER Ca(2+) store, efficient communications between the ER and the PM are critical for the homeostatic regulation of the PI(4,5)P2-Ca(2+) signaling system. This review describes the major findings that established the framework of the PI(4,5)P2-Ca(2+) signaling system, and recent discoveries on feedback control mechanisms at ER-PM junctions that sustain the PI(4,5)P2-Ca(2+) signaling system. Particular emphasis is placed on the characterization of ER-PM junctions where efficient communications between the ER and the PM occur, and the activation mechanisms of proteins that dynamically localize to ER-PM junctions to provide the feedback control during PI(4,5)P2-Ca(2+) signaling, including the ER Ca(2+) sensor STIM1, the extended synaptotagmin E-Syt1, and the PI transfer protein Nir2. This article is part of a Special Issue entitled: The cellular lipid landscape edited by Tim P. Levine and Anant K. Menon.

Indexed as

AnimalsCalciumCalcium ChannelsCalcium SignalingCell MembraneEndoplasmic ReticulumHomeostasisHumansMembrane ProteinsNeoplasm ProteinsORAI1 ProteinPhosphatidylinositol 4,5-DiphosphateStromal Interaction Molecule 1CalciumCalcium ChannelsMembrane ProteinsNeoplasm ProteinsORAI1 ProteinORAI1 protein, humanPhosphatidylinositol 4,5-DiphosphateSTIM1 protein, humanStromal Interaction Molecule 1ER–PM junctionsESyt1Nir2PI(4,5)P(2)–Ca(2+) signalingPI cycleSOCE

Identifiers

PMID26924250
PMCPMC4907847
OpenAlexW2286280596

What OpenQuestion holds

Textmetadata
LicenceTDM
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.