Evidence map›Paper›PMID 28583253›Full record

ArticleeLife2017

Loss of adult skeletal muscle stem cells drives age-related neuromuscular junction degeneration.

Wenxuan Liu, Alanna Klose, Sophie Forman, Nicole D Paris, Lan Wei-LaPierre, Mariela Cortés-Lopéz, Aidi Tan, Morgan Flaherty, Pedro Miura, Robert T Dirksen and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

115 citing papers in PubMed, 1 synthesis or guideline pooled it, 183 citations in OpenAlex.

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55 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

11 authors at 4 institutions in 2 countries.

Wenxuan LiuDepartment of Orthopaedics and Rehabilitation, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, United States.
Alanna KloseDepartment of Orthopaedics and Rehabilitation, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, United States.
Sophie FormanDepartment of Biology, University of Rochester, Rochester, United States.
Nicole D ParisDepartment of Orthopaedics and Rehabilitation, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, United States.ORCID 0000-0003-0654-0983
Lan Wei-LaPierreDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, United States.
Mariela Cortés-LopézDepartment of Biology, University of Nevada, Reno, United States.
Aidi TanBioinformatics Division and Center for Synthetic and Systems Biology, Tsinghua University, Beijing, China.
Morgan FlahertyDepartment of Biomedical Genetics, University of Rochester Medical Center, Rochester, United States.
Pedro MiuraDepartment of Biology, University of Nevada, Reno, United States.
Robert T DirksenDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, United States.
Joe V ChakkalakalDepartment of Orthopaedics and Rehabilitation, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, United States.ORCID 0000-0002-8440-7312
University of Rochester Medical Center · USUniversity of Nevada, Reno · USTsinghua University · CNUniversity of Rochester · US

Funding

Interrelationships between age-related skeletal muscle stem cell and NMJ declineR01AG051456 · NIA · UNIVERSITY OF ROCHESTER · PI CHAKKALAKAL, JOE · 2015 to 2019
$1.9M
Cellular Basis for Radiation induced acceleration of sarcopenia in juvenile cancer survivorsR01CA220467 · NCI · UNIVERSITY OF ROCHESTER · PI CHAKKALAKAL, JOE · 2017 to 2021
$1.8M
NCI NIH HHS R01 CA220467NIA NIH HHS R01 AG051456
6 · The paper itself

Abstract

Neuromuscular junction degeneration is a prominent aspect of sarcopenia, the age-associated loss of skeletal muscle integrity. Previously, we showed that muscle stem cells activate and contribute to mouse neuromuscular junction regeneration in response to denervation (Liu et al., 2015). Here, we examined gene expression profiles and neuromuscular junction integrity in aged mouse muscles, and unexpectedly found limited denervation despite a high level of degenerated neuromuscular junctions. Instead, degenerated neuromuscular junctions were associated with reduced contribution from muscle stem cells. Indeed, muscle stem cell depletion was sufficient to induce neuromuscular junction degeneration at a younger age. Conversely, prevention of muscle stem cell and derived myonuclei loss was associated with attenuation of age-related neuromuscular junction degeneration, muscle atrophy, and the promotion of aged muscle force generation. Our observations demonstrate that deficiencies in muscle stem cell fate and post-synaptic myogenesis provide a cellular basis for age-related neuromuscular junction degeneration and associated skeletal muscle decline.

Indexed as

AgingAnimalsMiceMuscle, SkeletalNeuromuscular JunctionSarcopeniaStem Cellsagingdenervationdevelopmental biologymousesarcopeniasatellite cellSproutystem cellssynapse

Identifiers

PMID28583253
PMCPMC5462534
OpenAlexW2622591269

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.