Evidence map›Paper›PMID 26203859›Full record

ReviewCell death & disease2015

Interactions between muscle stem cells, mesenchymal-derived cells and immune cells in muscle homeostasis, regeneration and disease.

J Farup, L Madaro, P L Puri, U R Mikkelsen

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04998500 (Growth Hormone as a Model for Reversible Activation of Adipose Tissue Fibrosis), which is not on this map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
5.1field-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.

NCT04998500 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Growth Hormone as a Model for Reversible Activation of Adipose Tissue Fibrosis

TypeinterventionalSponsorUniversity of AarhusRan2021 to 2023Enrolled10ConditionsFibrosisArmsGrowth hormone, saline and GH receptor blockade (Pegvisomant)
3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 164 citations in OpenAlex.

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  12. Effects of DietaryVeterinary sciences · 2025
    Article
  13. Review
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  15. Article
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  20. FAPs orchestrate homeostasis of muscle physiology and pathophysiology.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Review

37 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

4 authors at 4 institutions in 3 countries.

J FarupSection for Sports Science, Institute of Public Health, Aarhus University, Aarhus, Denmark.
L Madaro1] Sanford-Burnham Medical Research Institute, Sanford Children's Health Research Center, La Jolla, CA, USA [2] IRCCS Fondazione Santa Lucia, Rome, Italy.
P L Puri1] Sanford-Burnham Medical Research Institute, Sanford Children's Health Research Center, La Jolla, CA, USA [2] IRCCS Fondazione Santa Lucia, Rome, Italy.
U R Mikkelsen1] Section for Sports Science, Institute of Public Health, Aarhus University, Aarhus, Denmark [2] Institute of Sports Medicine, Department of Orthopaedic Surgery M, Bispebjerg Hospital and Center for Healthy Aging, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Aarhus University · DKBispebjerg Hospital · DKFondazione Santa Lucia · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

Pathogenic Alterations of the 3D Epigenetic Landscape in Dystrophin-Deficient Skeletal Muscles and Reversal by Dystrophin Re-ExpressionR01AR056712 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Pier Lorenzo Puri · 2009 to 2026
$7.3M
Signal-dependent switch of SWI/SNF by miRNAs & control of muscle stem cell fateR01AR052779 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PURI, PIER LORENZO · 2006 to 2015
$4.1M
San Diego Skeletal Muscle Research CenterP30AR061303 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, JU · 2011 to 2015
$3.3M
NIAMS NIH HHS P30 AR061303NIAMS NIH HHS R01 AR052779NIAMS NIH HHS R01AR052779NIAMS NIH HHS R01 AR056712NIAMS NIH HHS R01AR056712
6 · The paper itself

Abstract

Recent evidence has revealed the importance of reciprocal functional interactions between different types of mononuclear cells in coordinating the repair of injured muscles. In particular, signals released from the inflammatory infiltrate and from mesenchymal interstitial cells (also known as fibro-adipogenic progenitors (FAPs)) appear to instruct muscle stem cells (satellite cells) to break quiescence, proliferate and differentiate. Interestingly, conditions that compromise the functional integrity of this network can bias muscle repair toward pathological outcomes that are typically observed in chronic muscular disorders, that is, fibrotic and fatty muscle degeneration as well as myofiber atrophy. In this review, we will summarize the current knowledge on the regulation of this network in physiological and pathological conditions, and anticipate the potential contribution of its cellular components to relatively unexplored conditions, such as aging and physical exercise.

Indexed as

AdipocytesCell CommunicationCell DifferentiationEosinophilsFibroblastsHomeostasisHumansMacrophagesMesenchymal Stem CellsMuscle DevelopmentMuscle, SkeletalMuscular Dystrophy, DuchenneRegenerationSatellite Cells, Skeletal Muscle

Identifiers

PMID26203859
PMCPMC4650743
OpenAlexW1511347124

What OpenQuestion holds

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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 OpenQuestion graph.