Evidence map›Paper›PMID 30139748›Full record

ArticleThe Journal of biological chemistry2018

Biological scaffold-mediated delivery of myostatin inhibitor promotes a regenerative immune response in an animal model of Duchenne muscular dystrophy.

Kenneth M Estrellas, Liam Chung, Lindsay A Cheu, Kaitlyn Sadtler, Shoumyo Majumdar, Jyothi Mula, Matthew T Wolf, Jennifer H Elisseeff, Kathryn R Wagner

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  6. Harnessing Biomaterials for Immunomodulatory-Driven Tissue Engineering.Regenerative engineering and translational medicine · 2023
    Review
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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

9 authors at 6 institutions in 1 country.

Kenneth M EstrellasFrom the Hugo W. Moser Research Institute at Kennedy Krieger, Baltimore, Maryland 21205.ORCID 0000-0003-0413-6258
Liam Chungthe Translational Tissue Engineering Center and.ORCID 0000-0002-3919-6253
Lindsay A Cheuthe Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611.
Kaitlyn Sadtlerthe David H. Koch Institute for Integrative Cancer Research, Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142.
Shoumyo Majumdarthe Translational Tissue Engineering Center and.
Jyothi Mulathe NCI at Frederick, National Institutes of Health, Frederick, Maryland 21702, and.
Matthew T Wolfthe Translational Tissue Engineering Center and.
Jennifer H Elisseeffthe Translational Tissue Engineering Center and jhe@jhu.edu.
Kathryn R WagnerFrom the Hugo W. Moser Research Institute at Kennedy Krieger, Baltimore, Maryland 21205, wagnerk@kennedykrieger.org.
Johns Hopkins University · USBoston Children's Hospital · USJohns Hopkins Medicine · USKennedy Krieger Institute · USNational Institutes of Health · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have reported that the immune system significantly mediates skeletal muscle repair and regeneration. Additionally, biological scaffolds have been shown to play a role in polarizing the immune microenvironment toward pro-myogenic outcomes. Moreover, myostatin inhibitors are known to promote muscle regeneration and ameliorate fibrosis in animal models of Duchenne muscular dystrophy (DMD), a human disease characterized by chronic muscle degeneration. Biological scaffolds and myostatin inhibition can potentially influence immune-mediated regeneration in the dystrophic environment, but have not been evaluated together. Toward this end, here we created an injectable biological scaffold composed of hyaluronic acid and processed skeletal muscle extracellular matrix. This material formed a cytocompatible hydrogel at physiological temperatures

Indexed as

Absorbable ImplantsAnimalsAntibodies, MonoclonalDrug Delivery SystemsExtracellular MatrixForkhead Transcription FactorsGene Expression RegulationHumansHyaluronic AcidHydrogelsImmunity, InnateLectins, C-TypeMacrophagesMannose-Binding LectinsMannose ReceptorMiceAntibodies, MonoclonalForkhead Transcription FactorsFoxp3 protein, mouseHyaluronic AcidHydrogelsLectins, C-TypeMannose-Binding LectinsMannose ReceptorMstn protein, mouseMyostatinReceptors, Cell Surfacebioengineeringbiomaterialscytokinedrug deliverydystrophinextracellular matrixhydrogelimmunologymdxmusclemuscle regenerationmuscular dystrophymyostatinstem cells

Identifiers

PMID30139748
PMCPMC6177591
OpenAlexW2888475321

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.