Evidence map›Paper›PMID 20359506›Full record

ArticleBiochimica et biophysica acta2010

Calcineurin signaling and PGC-1alpha expression are suppressed during muscle atrophy due to diabetes.

Tiffany K Roberts-Wilson, Ramesh N Reddy, James L Bailey, Bin Zheng, Ronald Ordas, Jennifer L Gooch, S Russ Price

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-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

29 citing papers in PubMed, 51 citations in OpenAlex.

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  13. Ambient and supplemental magnetic fields promote myogenesisFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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  16. MicroRNA-23a and MicroRNA-27a Mimic Exercise by Ameliorating CKD-Induced Muscle Atrophy.Journal of the American Society of Nephrology : JASN · 2017
    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

7 authors at 1 institution in 1 country.

Tiffany K Roberts-WilsonRenal Division, School of Medicine, Emory University, Atlanta, GA 30322, USA.
Ramesh N Reddy
James L Bailey
Bin Zheng
Ronald Ordas
Jennifer L Gooch
S Russ Price
Emory University · US

Funding

Tissue Culture CoreP01DK061521 · NIDDK · EMORY UNIVERSITY · PI EATON, DOUGLAS C. · 2004 to 2009
$6.5M
TISSUE SPECIFIC NUTRITIONAL ADAPTATIONS IN RENAL FAILURER01DK050740 · NIDDK · EMORY UNIVERSITY · PI PRICE, S. RUSS · 1996 to 2010
$2.0M
Specificity of Calcineurin Signaling in the KidneyR01DK066422 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI GOOCH, JENNIFER L · 2004 to 2007
$959k
NIDDK NIH HHS DK066422NIDDK NIH HHS DK50740NIDDK NIH HHS DK61521NIDDK NIH HHS P01 DK061521NIDDK NIH HHS R01 DK050740NIDDK NIH HHS R01 DK066422
6 · The paper itself

Abstract

PGC-1alpha is a transcriptional coactivator that controls energy homeostasis through regulation of glucose and oxidative metabolism. Both PGC-1alpha expression and oxidative capacity are decreased in skeletal muscle of patients and animals undergoing atrophy, suggesting that PGC-1alpha participates in the regulation of muscle mass. PGC-1alpha gene expression is controlled by calcium- and cAMP-sensitive pathways. However, the mechanism regulating PGC-1alpha in skeletal muscle during atrophy remains unclear. Therefore, we examined the mechanism responsible for decreased PGC-1alpha expression using a rodent streptozotocin (STZ) model of chronic diabetes and atrophy. After 21days, the levels of PGC-1alpha protein and mRNA were decreased. We examined the activation state of CREB, a potent activator of PGC-1alpha transcription, and found that phospho-CREB was paradoxically high in muscle of STZ-rats, suggesting that the cAMP pathway was not involved in PGC-1alpha regulation. In contrast, expression of calcineurin (Cn), a calcium-dependent phosphatase, was suppressed in the same muscles. PGC-1alpha expression is regulated by two Cn substrates, MEF2 and NFATc. Therefore, we examined MEF2 and NFATc activity in muscles from STZ-rats. Target genes MRF4 and MCIP1.4 mRNAs were both significantly reduced, consistent with reduced Cn signaling. Moreover, levels of MRF4, MCIP1.4, and PGC-1alpha were also decreased in muscles of CnAalpha-/- and CnAbeta-/- mice without diabetes indicating that decreased Cn signaling, rather than changes in other calcium- or cAMP-sensitive pathways, were responsible for decreased PGC-1alpha expression. These findings demonstrate that Cn activity is a major determinant of PGC-1alpha expression in skeletal muscle during diabetes and possibly other conditions associated with loss of muscle mass.

Indexed as

Muscular AtrophyAnimalsCalcineurinCyclic AMP Response Element-Binding ProteinDiabetes ComplicationsDiabetes Mellitus, ExperimentalHumansMaleMiceMuscle, SkeletalMyogenic Regulatory FactorsNFATC Transcription FactorsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaRatsRats, Sprague-DawleyRNA-Binding ProteinsCalcineurinCyclic AMP Response Element-Binding ProteinMyogenic Regulatory FactorsNFATC Transcription FactorsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mousePpargc1a protein, ratRNA-Binding ProteinsTrans-ActivatorsTranscription Factors

Identifiers

PMID20359506
PMCPMC2885580
OpenAlexW2157281277

What OpenQuestion 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 OpenQuestion graph.