Evidence map›Paper›PMID 31266969›Full record

ArticleScientific reports2019

Critical Limb Ischemia Induces Remodeling of Skeletal Muscle Motor Unit, Myonuclear-, and Mitochondrial-Domains.

Mahir Mohiuddin, Nan Hee Lee, June Young Moon, Woojin M Han, Shannon E Anderson, Jeongmoon J Choi, Eunjung Shin, Shadi A Nakhai, Thu Tran, Berna Aliya and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05671614 (Skeletal Muscle Regeneration in Survivors of Critical Illness), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

NCT05671614 recruitingnot on this mapstarted 2022, after this paper: background citation

Skeletal Muscle Regeneration in Survivors of Critical Illness: How to Prevent Satellite Cell Failure?

TypeobservationalSponsorCharles University, Czech RepublicRan2022 to 2025Enrolled50ConditionsIntensive Care Unit-acquired Weakness
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  18. A Hydrogel Strategy to Augment Tissue Adenosine to Improve Hindlimb Perfusion.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Article
  19. Secondary denervation is a chronic pathophysiologic sequela of volumetric muscle loss.Journal of applied physiology (Bethesda, Md. : 1985) · 2021
    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

15 authors at 2 institutions in 1 country.

Mahir MohiuddinSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Nan Hee LeeSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
June Young MoonSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Woojin M HanParker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Shannon E AndersonWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, 30332, USA.
Jeongmoon J ChoiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.ORCID http://orcid.org/0000-0003-1726-5278
Eunjung ShinSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Shadi A NakhaiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Thu TranSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Berna AliyaSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Do Young KimSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Aimee GeroldWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, 30332, USA.
Laura M HansenDivision of Cardiology, Emory University School of Medicine, Atlanta, GA, 30322, USA.
W Robert TaylorDivision of Cardiology, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Young C JangSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA. young.jang@gatech.edu.
Georgia Institute of Technology · USEmory University · US

Funding

Research Training Program Plan on Cell and Tissue Engineering (CTEng)T32GM008433 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 1991 to 2021
$7.1M
IVIS Spectrum in vivo Imaging SystemS10OD016264 · OD · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 2015 to 2015
$595k
Implantable biofunctional hydrogel for muscle stem cell transplantationR21AR072287 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI JANG, YOUNG CHARLES · 2017 to 2018
$377k
NIAMS NIH HHS R21 AR072287NIGMS NIH HHS T32 GM008433NIH HHS S10 OD016264
6 · The paper itself

Abstract

Critical limb ischemia, the most severe form of peripheral artery disease, leads to extensive damage and alterations to skeletal muscle homeostasis. Although recent research has investigated the tissue-specific responses to ischemia, the role of the muscle stem cell in the regeneration of its niche components within skeletal muscle has been limited. To elucidate the regenerative mechanism of the muscle stem cell in response to ischemic insults, we explored cellular interactions between the vasculature, neural network, and muscle fiber within the muscle stem cell niche. Using a surgical murine hindlimb ischemia model, we first discovered a significant increase in subsynaptic nuclei and remodeling of the neuromuscular junction following ischemia-induced denervation. In addition, ischemic injury causes significant alterations to the myofiber through a muscle stem cell-mediated accumulation of total myonuclei and a concomitant decrease in myonuclear domain size, possibly to enhance the transcriptional and translation output and restore muscle mass. Results also revealed an accumulation of total mitochondrial content per myonucleus in ischemic myofibers to compensate for impaired mitochondrial function and high turnover rate. Taken together, the findings from this study suggest that the muscle stem cell plays a role in motor neuron reinnervation, myonuclear accretion, and mitochondrial biogenesis for skeletal muscle regeneration following ischemic injury.

Indexed as

Neuromuscular JunctionAnimalsDisease Models, AnimalExtremitiesIschemiaMiceMitochondria, MuscleMuscle, SkeletalMyoblastsRegeneration

Identifiers

PMID31266969
PMCPMC6606576
OpenAlexW2954454316

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.