Evidence map›Paper›PMID 37534432›Full record

ArticleJournal of cell science2023

A novel homeostatic mechanism tunes PI(4,5)P2-dependent signaling at the plasma membrane.

Rachel C Wills, Colleen P Doyle, James P Zewe, Jonathan Pacheco, Scott D Hansen, Gerald R V Hammond

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed, 31 citations in OpenAlex.

  1. PI(3,5)PScience advances · 2026
    Article
  2. Review
  3. Article
  4. PIP4K attenuates PIP5K lipid kinase activity by disrupting membrane-mediated dimerization.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Subcellular Cartography of the Phosphoinositide Multiverse.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2026
    Review
  7. Distinct impact of PI(4)P flux on PI(4,5)PProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. PI(4,5)PBiochimica et biophysica acta. Molecular and cell biology of lipids · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Nonlinear dynamics in phosphoinositide metabolism.Current opinion in cell biology · 2024
    Review
  17. Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

Rachel C WillsDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.ORCID 0000-0003-2161-9235
Colleen P DoyleDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.ORCID 0000-0002-3326-792X
James P ZeweDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Jonathan PachecoDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Scott D HansenDepartment of Chemistry and Biochemistry, University of Oregon, Eugene, OR 97403, USA.
Gerald R V HammondDepartment of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.ORCID 0000-0002-6660-3272
University of Pittsburgh · USUniversity of Oregon · US

Funding

Directing Membrane Function with Inositol Lipids in Health and DiseaseR35GM119412 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Gerald R Hammond · 2016 to 2026
$4.3M
PIP5K1A as a novel driver of PI3K signaling in health and diseaseR03TR003624 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HAMMOND, GERALD R · 2021 to 2021
$157k
PIP5K1A Enhances Phosphoinositide Signaling to Drive Breast CancerF31CA247349 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WILLS, RACHEL · 2020 to 2021
$92k
NCATS NIH HHS R03 TR003624NCI NIH HHS F31 CA247349NIGMS NIH HHS R35 GM119412NIH HHS 2R35GM119412
6 · The paper itself

Abstract

The lipid molecule phosphatidylinositol (4,5)-bisphosphate [PI(4,5)P2] controls all aspects of plasma membrane (PM) function in animal cells, from its selective permeability to the attachment of the cytoskeleton. Although disruption of PI(4,5)P2 is associated with a wide range of diseases, it remains unclear how cells sense and maintain PI(4,5)P2 levels to support various cell functions. Here, we show that the PIP4K family of enzymes, which synthesize PI(4,5)P2 via a minor pathway, also function as sensors of tonic PI(4,5)P2 levels. PIP4Ks are recruited to the PM by elevated PI(4,5)P2 levels, where they inhibit the major PI(4,5)P2-synthesizing PIP5Ks. Perturbation of this simple homeostatic mechanism reveals differential sensitivity of PI(4,5)P2-dependent signaling to elevated PI(4,5)P2 levels. These findings reveal that a subset of PI(4,5)P2-driven functions might drive disease associated with disrupted PI(4,5)P2 homeostasis.

Indexed as

Phosphatidylinositol 4,5-DiphosphateSignal TransductionAnimalsCell MembraneHomeostasisPhosphatidylinositolsPhosphatidylinositol 4,5-DiphosphatePhosphatidylinositolsPhosphoinositidePI3KPIPKPlasma membranePLCPtdInsSignaling

Identifiers

PMID37534432
PMCPMC10482388
OpenAlexW4385514877

What Socratic 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 Socratic graph.