Evidence map›Paper›PMID 15282035›Full record

ArticleBMC cell biology2004

Calcineurin activation influences muscle phenotype in a muscle-specific fashion.

Robert J Talmadge, Jeffrey S Otis, Matthew R Rittler, Nicole D Garcia, Shelly R Spencer, Simon J Lees, Francisco J Naya

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Calcineurin: a poorly understood regulator of muscle mass.The international journal of biochemistry & cell biology · 2013
    Review
  14. Article
  15. Genetic deletion of trkB.T1 increases neuromuscular function.American journal of physiology. Cell physiology · 2012
    Article
  16. Article
  17. Myospryn is a calcineurin-interacting protein that negatively modulates slow-fiber-type transformation and skeletal muscle regeneration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  18. Article
  19. Are calcineurin genes associated with endurance phenotype traits?European journal of applied physiology · 2010
    Article
  20. Article
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 3 institutions in 1 country.

Robert J TalmadgeDepartment of Biological Sciences, California State Polytechnic University, Pomona, CA 91768, USA. rjtalmadge@csupomona.edu
Jeffrey S Otis
Matthew R Rittler
Nicole D Garcia
Shelly R Spencer
Simon J Lees
Francisco J Naya
California State Polytechnic University · USVirginia Tech · USThe University of Texas Southwestern Medical Center · US

Funding

The Response of Choline and Folate Status to Controlled Levels of Choline IntakeS06GM053933 · NIGMS · CALIFORNIA STATE POLY U POMONA · PI CAUDILL, MARIE A · 1997 to 2007
$15.1M
NIGMS NIH HHS S06 GM053933NIGMS NIH HHS S06 GM53933
6 · The paper itself

Abstract

backgroundThe calcium activated protein phosphatase 2B, also known as calcineurin, has been implicated as a cell signaling molecule involved with transduction of physiological signals (free cytosolic Ca2+) into molecular signals that influence the expression of phenotype-specific genes in skeletal muscle. In the present study we address the role of calcineurin in mediating adaptations in myosin heavy chain (MHC) isoform expression and muscle mass using 3-month old wild-type (WT) and transgenic mice displaying high-level expression of a constitutively active form of calcineurin (MCK-CN* mice).

resultsSlow muscles, e.g., soleus, were significantly larger (by ~24%), whereas fast muscles, e.g., medial gastrocnemius (MG) and tibialis anterior were significantly smaller (by ~26 and ~16%, respectively) in MCK-CN* mice compared to WT. The masses of mixed phenotype muscles, such as the plantaris and the extensor digitorum longus, were not significantly changed from WT. The soleus, plantaris, MG and diaphragm displayed shifts toward slower MHC isoforms, e.g., soleus from WT mice contained ~52% MHC-I, ~39% MHC-IIa, and ~9% MHC-IIx, whereas MCK-CN* mice had ~67% MHC-I, ~26% MHC-IIa, and ~7% MHC-IIx. The specific isoforms that were either up or down-regulated were muscle-specific. For instance, the proportion of MHC-IIa was decreased in the soleus and diaphragm, but increased in the plantaris and MG of MCK-CN* mice. Also, the proportion of MHC-IIx was unchanged in the soleus, decreased in the diaphragm and increased in the plantaris and MG of MCK-CN* relative to WT mice. Fast to slow shifts in fiber type proportions were evident for the plantaris, but not the soleus. Fast, but not slow, plantaris fibers of MCK-CN* mice had higher oxidative and lower glycolytic properties than WT.

conclusionThese data suggest that calcineurin activation can influence muscle phenotype and that the specific influence of calcineurin activation on the phenotypic and mass characteristics of a muscle is dependent upon the original phenotypic state of the muscle.

Indexed as

Adaptation, PhysiologicalAnimalsCalcineurinEnzyme ActivationGlycerolphosphate DehydrogenaseMiceMice, TransgenicMuscle Fibers, Fast-TwitchMuscle Fibers, Slow-TwitchMuscle, SkeletalMyosin Heavy ChainsPhenotypeProtein IsoformsSuccinate DehydrogenaseCalcineurinGlycerolphosphate DehydrogenaseMyosin Heavy ChainsProtein IsoformsSuccinate Dehydrogenase

Identifiers

PMID15282035
PMCPMC509416
OpenAlexW2152252765

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.