Evidence map›Paper›PMID 26035394›Full record

ArticleDisease models & mechanisms2015

Phospholamban overexpression in mice causes a centronuclear myopathy-like phenotype.

Val A Fajardo, Eric Bombardier, Elliott McMillan, Khanh Tran, Brennan J Wadsworth, Daniel Gamu, Andrew Hopf, Chris Vigna, Ian C Smith, Catherine Bellissimo and 4 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

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  13. Increase in phospholamban content in mouse skeletal muscle after denervation.Journal of muscle research and cell motility · 2018
    Article
  14. Article
  15. Article
  16. Sarcolipin: A Key Thermogenic and Metabolic Regulator in Skeletal Muscle.Trends in endocrinology and metabolism: TEM · 2016
    Review
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  18. Article
  19. 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

14 authors at 3 institutions in 1 country.

Val A FajardoDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Eric BombardierDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Elliott McMillanDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Khanh TranDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Brennan J WadsworthDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Daniel GamuDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Andrew HopfDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Chris VignaDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Ian C SmithDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Catherine BellissimoDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Robin N MichelDepartment of Exercise Science, Concordia University, Montreal, Quebec H4B 1R6, Canada.
Mark A TarnopolskyDepartement of Kinesiology, McMaster University, Hamilton, Ontario L8N 3Z5, Canada Department of Pediatrics, McMaster University, Hamilton, Ontario L8N 3Z5, Canada Department of Medicine, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
Joe QuadrilateroDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
A Russell TuplingDepartment of Kinesiology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada rtupling@uwaterloo.ca.
University of Waterloo · CAConcordia University · CAMcMaster University · CA

Funding

Canadian Institutes of Health Research MOP 47296Canadian Institutes of Health Research MOP 86618
6 · The paper itself

Abstract

Centronuclear myopathy (CNM) is a congenital myopathy that is histopathologically characterized by centrally located nuclei, central aggregation of oxidative activity, and type I fiber predominance and hypotrophy. Here, we obtained commercially available mice overexpressing phospholamban (Pln(OE)), a well-known inhibitor of sarco(endo)plasmic reticulum Ca(2+)-ATPases (SERCAs), in their slow-twitch type I skeletal muscle fibers to determine the effects on SERCA function. As expected with a 6- to 7-fold overexpression of phospholamban, SERCA dysfunction was evident in Pln(OE) muscles, with marked reductions in rates of Ca(2+) uptake, maximal ATPase activity and the apparent affinity of SERCA for Ca(2+). However, our most significant discovery was that the soleus and gluteus minimus muscles from the Pln(OE) mice displayed overt signs of myopathy: they histopathologically resembled human CNM, with centrally located nuclei, central aggregation of oxidative activity, type I fiber predominance and hypotrophy, progressive fibrosis and muscle weakness. This phenotype is associated with significant upregulation of muscle sarcolipin and dynamin 2, increased Ca(2+)-activated proteolysis, oxidative stress and protein nitrosylation. Moreover, in our assessment of muscle biopsies from three human CNM patients, we found a significant 53% reduction in SERCA activity and increases in both total and monomeric PLN content compared with five healthy subjects, thereby justifying future studies with more CNM patients. Altogether, our results suggest that the commercially available Pln(OE) mouse phenotypically resembles human CNM and could be used as a model to test potential mechanisms and therapeutic strategies. To date, there is no cure for CNM and our results suggest that targeting SERCA function, which has already been shown to be an effective therapeutic target for murine muscular dystrophy and human cardiomyopathy, might represent a novel therapeutic strategy to combat CNM.

Indexed as

AdolescentAdultAnimalsCalciumCalcium-Binding ProteinsDynamin IIFibrosisHumansMaleMiceMusclesMuscular AtrophyMuscular Dystrophy, AnimalMyopathies, Structural, CongenitalOxidative StressPhenotypeCalciumCalcium-Binding ProteinsDynamin IIPhospholambanSarcoplasmic Reticulum Calcium-Transporting ATPasesCalcium regulationCongenital myopathyDynamin 2SERCASkeletal muscle

Identifiers

PMID26035394
PMCPMC4527296
OpenAlexW2100474560

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.