Evidence map›Paper›PMID 35318675›Full record

ArticleThe Journal of physiology2023

Development of a cell-free strategy to recover aged skeletal muscle after disuse.

Yu-Fu Wu, Eduardo A De La Toba, Svyatoslav Dvoretskiy, Rebecca Jung, Noah Kim, Laureen Daniels, Elena V Romanova, Jenny Drnevich, Jonathan V Sweedler, Marni D Boppart

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Exercise Training Stimulates the Release of Glutathione Peroxidase 1 (GPX1)-Enriched Extracellular Vesicles That Promote Angiogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Plasma-Derived Extracellular Vesicle Proteomics.Journal of proteome research · 2025
    Review
  11. Article
  12. Macrophage immunometabolism: emerging targets for regrowth in aging muscle.American journal of physiology. Endocrinology and metabolism · 2025
    Review
  13. Review
  14. Article
  15. MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury.Cellular and molecular life sciences : CMLS · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Yu-Fu WuDepartment of Kinesiology and Community Health, University of Illinois, Urbana, Illinois, USA.
Eduardo A De La TobaBeckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, USA.
Svyatoslav DvoretskiyDepartment of Kinesiology and Community Health, University of Illinois, Urbana, Illinois, USA.
Rebecca JungBeckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, USA.
Noah KimDepartment of Kinesiology and Community Health, University of Illinois, Urbana, Illinois, USA.
Laureen DanielsBeckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, USA.
Elena V RomanovaBeckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, USA.
Jenny DrnevichRoy J. Carver Biotechnology Center, High Performance Biological Computing, University of Illinois, Urbana, Illinois, USA.
Jonathan V SweedlerBeckman Institute for Advanced Science and Technology, University of Illinois, Urbana, Illinois, USA.
Marni D BoppartDepartment of Kinesiology and Community Health, University of Illinois, Urbana, Illinois, USA.ORCID 0000-0003-0369-6974
University of Illinois Urbana-Champaign · US

Funding

The UIUC Neuroproteomics Center on Cell-Cell SignalingP30DA018310 · NIDA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI Jonathan V. Sweedler · 2004 to 2026
$24.9M
Development of a Cell-Based Therapy to Improve Recovery Following ImmobilizationR01AR072735 · NIAMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI BOPPART, MARNI D. · 2018 to 2022
$1.7M
NIAMS NIH HHS R01 AR072735NIDA NIH HHS P30 DA018310NIH HHS P30 DA018310NIH HHS R01 AR072735
6 · The paper itself

Abstract

Extended periods of bed rest and limb immobilization are required for healing post-injury or disease, yet disuse can result in significant muscle atrophy and decreased quality of life in older adults. Physical rehabilitation is commonly prescribed to recover these deficits, yet accumulation of reactive oxygen species and sustained rates of protein degradation persist during the rehabilitation period that can significantly delay or prevent recovery. Pericytes, considered the primary mesenchymal and vascular stromal cell in skeletal muscle, secrete beneficial factors that maintain baseline muscle mass, yet minimal information exists regarding the pericyte response to disuse and recovery. In the current study, single-cell RNA sequencing and functional assays were performed to demonstrate that pericytes in mouse skeletal muscle lose the capacity to synthesize antioxidants during disuse and recovery. This information was used to guide the design of a strategy in which healthy donor pericytes were stimulated with hydrogen peroxide (H

Indexed as

Hydrogen PeroxideQuality of LifeAnimalsAntioxidantsMiceMuscle, SkeletalMuscular AtrophyProteomicsAntioxidantsHydrogen Peroxideantioxidantdisuse atrophyextracellular vesiclespericyteskeletal muscle

Identifiers

PMID35318675
PMCPMC9492804
OpenAlexW4220814643

What Socratic 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 Socratic graph.