Evidence map›Paper›PMID 22325604›Full record

ArticleMethods in cell biology2012

Acute manipulation of phosphoinositide levels in cells.

Belle Chang-Ileto, Samuel G Frere, Gilbert Di Paolo

Abstract read
In one paragraph

Article in Methods in cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Sphingolipid homeostasis in the endoplasmic reticulum and beyond.Cold Spring Harbor perspectives in biology · 2013
    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

3 authors.

Belle Chang-IletoDepartment of Pathology and Cell Biology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, USA.
Samuel G Frere
Gilbert Di Paolo

Funding

Role of phospholipids in membrane traffic at the synapseR01NS056049 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LIEM, RONALD K. · 2006 to 2016
$3.7M
Role of PIP2 metabolism imbalance in Down SyndromeR01HD055457 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DI PAOLO, GILBERT · 2008 to 2012
$1.7M
Regulation of PIP2 Metabolism in Nerve TerminalsF31NS058096 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHANG, BELLE · 2007 to 2009
$123k
NICHD NIH HHS R01 HD055457NICHD NIH HHS R01 HD05547NINDS NIH HHS F31 NS058096NINDS NIH HHS R01 NS056049
6 · The paper itself

Abstract

Phosphoinositides are membrane-bound signaling phospholipids that function in a myriad of cellular processes, including membrane trafficking, cytoskeletal dynamics, ion channel and transporter function, and signal transduction. In order to better understand the role of phosphoinositides in cellular processes, different approaches to study the effects of the presence or absence of these lipids must be devised. Conventional approaches of manipulating phosphoinositide levels such as over-expression or genetic ablation of lipid enzymes cause prolonged exposure of the cells to changes in lipid levels that could result in compensatory actions by the cell or downstream alterations in cell physiology. In this chapter we present an approach used recently by various laboratories, including our own, to acutely manipulate phosphoinositide levels at target locations using chemically induced dimerization (CID) that can be spatially and temporally controlled. We discuss considerations when designing expression constructs for targeting specific cellular compartment membranes and present examples from the literature on different ways of perturbing phosphoinositide levels at particular organelle membranes using CID. In addition, we provide details on image acquisition, data collection, and data interpretation. CID technology can be applied to many lipid enzymes to broaden the understanding of the role lipid signaling plays in cell physiology.

Indexed as

AnimalsBinding SitesBiocatalysisBiomarkersBiosensing TechniquesCell MembraneCells, CulturedEscherichia coli ProteinsFluorescent DyesHumansMembrane FusionMicroscopy, FluorescencePeptide FragmentsPhosphatidylinositolsPhosphoenolpyruvate Sugar Phosphotransferase SystemProtein Interaction Domains and MotifsBiomarkersEIN protein, E coliEscherichia coli ProteinsFluorescent DyesPeptide FragmentsPhosphatidylinositolsPhosphoenolpyruvate Sugar Phosphotransferase SystemProtein Sorting SignalsRecombinant Fusion Proteins

Identifiers

PMID22325604
PMCPMC3543678

What OpenQuestion holds

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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.