Evidence map›Paper›PMID 22932683›Full record

ArticleAmerican journal of physiology. Cell physiology2012

Kinetics of nuclear-cytoplasmic translocation of Foxo1 and Foxo3A in adult skeletal muscle fibers.

Tova Neustadt Schachter, Tiansheng Shen, Yewei Liu, Martin F Schneider

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Mathematical Modeling of Nuclear Trafficking of FOXO Transcription Factors.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
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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

4 authors at 1 institution in 1 country.

Tova Neustadt SchachterDept. of Biochemistry and Molecular Biology, Univ. of Maryland School of Medicine, 108 North Greene St., Baltimore MD 21201-1503, USA. mschneid@umaryland.edu
Tiansheng Shen
Yewei Liu
Martin F Schneider
University of Maryland, Baltimore · US

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
Training Grant in Cardiac and Vascular Cell BiologyT32HL072751 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI FISHER, STEVEN A. · 2003 to 2013
$3.1M
Activity Dependent Signaling in Adult Skeletal Muscle Fiber PlasticityR01AR056477 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHNEIDER, MARTIN F · 2008 to 2012
$1.6M
NHLBI NIH HHS T32-HL-072751NIAMS NIH HHS R01 AR056477NIAMS NIH HHS R01-AR056477NIAMS NIH HHS T32 AR007592NIAMS NIH HHS T32-AR-007592
6 · The paper itself

Abstract

In skeletal muscle, the transcription factors Foxo1 and Foxo3A control expression of proteins that mediate muscle atrophy, making the nuclear concentration and nuclear-cytoplasmic movements of Foxo1 and Foxo3A of therapeutic interest in conditions of muscle wasting. Here, we use Foxo-GFP fusion proteins adenovirally expressed in cultured adult mouse skeletal muscle fibers to characterize the time course of nuclear efflux of Foxo1-GFP in response to activation of the insulin-like growth factor-1 (IGF-1)/phosphatidylinositol-3-kinase (PI3K)/Akt pathway to determine the time course of nuclear influx of Foxo1-GFP during inhibition of this pathway and to show that Akt mediates the efflux of nuclear Foxo1-GFP induced by IGF-1. Localization of endogenous Foxo1 in muscle fibers, as determined via immunocytochemistry, is consistent with that of Foxo1-GFP. Inhibition of the nuclear export carrier chromosome region maintenance 1 by leptomycin B (LMB) traps Foxo1 in the nucleus and results in a relatively rapid rate of Foxo1 nuclear accumulation, consistent with a high rate of nuclear-cytoplasmic shuttling of Foxo1 under control conditions before LMB application, with near balance of unidirectional influx and efflux. Expressed Foxo3A-GFP shuttles ∼20-fold more slowly than Foxo1-GFP. Our approach allows quantitative kinetic characterization of Foxo1 and Foxo3A nuclear-cytoplasmic movements in living muscle fibers under various experimental conditions.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCells, CulturedCytoplasmFatty Acids, UnsaturatedFemaleForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsImmunohistochemistryInsulin-Like Growth Factor IMiceMuscle Fibers, SkeletalPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktFatty Acids, UnsaturatedForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsFoxo1 protein, mouseFoxO3 protein, mouseinsulin-like growth factor-1, mouseInsulin-Like Growth Factor Ileptomycin BPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-akt

Identifiers

PMID22932683
PMCPMC3492827
OpenAlexW1976603669

What OpenQuestion holds

Textmetadata
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.