Evidence map›Paper›PMID 11359938›Full record

ArticleMolecular biology of the cell2001

Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.

C E Torgan, M P Daniels

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 62 citations in OpenAlex.

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  12. NFAT is a nerve activity sensor in skeletal muscle and controls activity-dependent myosin switching.Proceedings of the National Academy of Sciences of the United States of America · 2004
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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

2 authors at 1 institution in 1 country.

C E TorganLaboratory of Biochemical Genetics, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892-4036, USA.
M P Daniels
National Institutes of Health · US

Funding

Mechanisms of Central Nervous System Neuron DevelopmentZ01HL000158 · NHLBI · HEART, LUNG, AND BLOOD INSTITUTE · PI DANIELS, MATHEW P · 1995 to 2006
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6 · The paper itself

Abstract

Signals that determine fast- and slow-twitch phenotypes of skeletal muscle fibers are thought to stem from depolarization, with concomitant contraction and activation of calcium-dependent pathways. We examined the roles of contraction and activation of calcineurin (CN) in regulation of slow and fast myosin heavy chain (MHC) protein expression during muscle fiber formation in vitro. Myotubes formed from embryonic day 21 rat myoblasts contracted spontaneously, and approximately 10% expressed slow MHC after 12 d in culture, as seen by immunofluorescent staining. Transfection with a constitutively active form of calcineurin (CN*) increased slow MHC by 2.5-fold as determined by Western blot. This effect was attenuated 35% by treatment with tetrodotoxin and 90% by administration of the selective inhibitor of CN, cyclosporin A. Conversely, cyclosporin A alone increased fast MHC by twofold. Cotransfection with VIVIT, a peptide that selectively inhibits calcineurin-induced activation of the nuclear factor of activated T-cells, blocked the effect of CN* on slow MHC by 70% but had no effect on fast MHC. The results suggest that contractile activity-dependent expression of slow MHC is mediated largely through the CN-nuclear factor of activated T-cells pathway, whereas suppression of fast MHC expression may be independent of nuclear factor of activated T-cells.

Indexed as

Muscle DevelopmentNuclear ProteinsAnimalsCalcineurinCells, CulturedCyclosporineDNA-Binding ProteinsEnzyme InhibitorsImmunoblottingMicroscopy, FluorescenceMuscle ContractionMuscle Fibers, SkeletalMuscle, SkeletalMyosin Heavy ChainsNFATC Transcription FactorsProtein IsoformsCalcineurinCyclosporineDNA-Binding ProteinsEnzyme InhibitorsMyosin Heavy ChainsNFATC Transcription FactorsNuclear ProteinsProtein IsoformsTetrodotoxinTranscription Factors

Identifiers

PMID11359938
PMCPMC34600
OpenAlexW2091220110

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.