Evidence map›Paper›PMID 23941502›Full record

ArticleAging cell2014

Maintenance of muscle mass and load-induced growth in Muscle RING Finger 1 null mice with age.

Darren T Hwee, Leslie M Baehr, Andrew Philp, Keith Baar, Sue C Bodine

Open access · greenAbstract read
In one paragraph

Article in Aging cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Aerobic exercise augments muscle transcriptome profile of resistance exercise.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Androgens as the "old age stick" in skeletal muscle.Cell communication and signaling : CCS · 2025
    Review
  11. Article
  12. Muscle Disuse Atrophy.Advances in experimental medicine and biology · 2025
    Review
  13. Article
  14. Decoding the decline: unveiling drivers of sarcopenia.The Journal of clinical investigation · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

18 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Darren T HweeDepartments of Neurobiology, Physiology, and Behavior, University of California Davis, Davis, CA, 95616, USA; Molecular, Cellular and Integrative Physiology Graduate Group, University of California Davis, Davis, CA, 95616, USA.
Leslie M Baehr
Andrew Philp
Keith Baar
Sue C Bodine
University of California, Davis · US

Funding

Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
Glucocorticoid control of gene expression during skeletal muscle atrophyR01DK075801 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BODINE, SUE C, FURLOW, JOHN DAVID · 2008 to 2011
$1.4M
Medical Research Council MR/K00414X/1NHLBI NIH HHS T32 HL086350NHLBI NIH HHS T32HL086350NIDDK NIH HHS DK75801NIDDK NIH HHS R01 DK075801
6 · The paper itself

Abstract

Age-related loss of muscle mass occurs to varying degrees in all individuals and has a detrimental effect on morbidity and mortality. Muscle RING Finger 1 (MuRF1), a muscle-specific E3 ubiquitin ligase, is believed to mediate muscle atrophy through the ubiquitin proteasome system (UPS). Deletion of MuRF1 (KO) in mice attenuates the loss of muscle mass following denervation, disuse, and glucocorticoid treatment; however, its role in age-related muscle loss is unknown. In this study, skeletal muscle from male wild-type (WT) and MuRF1 KO mice was studied up to the age of 24 months. Muscle mass and fiber cross-sectional area decreased significantly with age in WT, but not in KO mice. In aged WT muscle, significant decreases in proteasome activities, especially 20S and 26S β5 (20-40% decrease), were measured and were associated with significant increases in the maladaptive endoplasmic reticulum (ER) stress marker, CHOP. Conversely, in aged MuRF1 KO mice, 20S or 26S β5 proteasome activity was maintained or decreased to a lesser extent than in WT mice, and no increase in CHOP expression was measured. Examination of the growth response of older (18 months) mice to functional overload revealed that old WT mice had significantly less growth relative to young mice (1.37- vs. 1.83-fold), whereas old MuRF1 KO mice had a normal growth response (1.74- vs. 1.90-fold). These data collectively suggest that with age, MuRF1 plays an important role in the control of skeletal muscle mass and growth capacity through the regulation of cellular stress.

Indexed as

Muscle DevelopmentAgingAnimalsBiomarkersBody WeightCapillariesEndoplasmic Reticulum StressGene Expression Regulation, DevelopmentalMiceMice, KnockoutMuscle Fibers, SkeletalMuscle ProteinsMusclesOrgan SizeOxidative StressProteasome Endopeptidase ComplexBiomarkersFbxo32 protein, mouseMuscle ProteinsProteasome Endopeptidase ComplexSKP Cullin F-Box Protein LigasesTrim63 protein, mouseTripartite Motif ProteinsUbiquitinUbiquitin-Protein Ligasesanabolic resistanceER Stresssarcopeniaubiquitin proteasome system

Identifiers

PMID23941502
PMCPMC3947038
OpenAlexW2056792074

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.