Evidence map›Paper›PMID 35378706›Full record

ArticleSub-cellular biochemistry2022

Roles for 3' Phosphoinositides in Macropinocytosis.

Joel A Swanson, Nobukazu Araki

Open access · greenAbstract read
In one paragraph

Article in Sub-cellular biochemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.0field-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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Macropinocytosis inFrontiers in plant science · 2023
    Article
  7. Review
  8. The orchestrated signaling by PI3Kα and PTEN at the membrane interface.Computational and structural biotechnology journal · 2022
    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 2 institutions in 2 countries.

Joel A SwansonDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA. jswan@umich.edu.
Nobukazu ArakiDepartment of Histology and Cell Biology, School of Medicine, Kagawa University, Miki, Kagawa, Japan.
Kagawa University · JPUniversity of Michigan–Ann Arbor · US

Funding

The Regulation of MacropinocytosisR35GM131720 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SWANSON, JOEL A · 2019 to 2023
$2.4M
NIGMS NIH HHS R35 GM131720
6 · The paper itself

Abstract

The distinct movements of macropinosome formation and maturation have corresponding biochemical activities which occur in a defined sequence of stages and transitions between those stages. Each stage in the process is regulated by variously phosphorylated derivatives of phosphatidylinositol (PtdIns) which reside in the cytoplasmic face of the membrane lipid bilayer. PtdIns derivatives phosphorylated at the 3' position of the inositol moiety, called 3' phosphoinositides (3'PIs), regulate different stages of the sequence. 3'PIs are synthesized by numerous phosphoinositide 3'-kinases (PI3K) and other lipid kinases and phosphatases, which are themselves regulated by small GTPases of the Ras superfamily. The combined actions of these enzymes localize four principal species of 3'PI to distinct domains of the plasma membrane or to discrete organelles, with distinct biochemical activities confined to those domains. Phosphatidylinositol (3,4,5)-trisphosphate (PtdIns(3,4,5)P

Indexed as

PhosphatidylinositolsPinocytosisCell MembraneEndosomesPhosphoric Monoester HydrolasesPhosphatidylinositolsPhosphoric Monoester HydrolasesMacrophageMacropinosome closurePhosphatidylinositol 3-kinaseRuffling

Identifiers

PMID35378706
PMCPMC9910326
OpenAlexW4225540737

What Socratic 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 Socratic graph.