Evidence map›Paper›PMID 34551191›Full record

ArticleJournal of tissue engineering and regenerative medicine2021

Co-delivery of fibrin-laminin hydrogel with mesenchymal stem cell spheroids supports skeletal muscle regeneration following trauma.

Peter Genovese, Anjali Patel, Natalia Ziemkiewicz, Allison Paoli, Joseph Bruns, Natasha Case, Silviya P Zustiak, Koyal Garg

Open access · greenAbstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2021. 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
3.3field-weighted citation impact, top 7% 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, 27 citations in OpenAlex.

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  13. Porous biomaterial scaffolds for skeletal muscle tissue engineering.Frontiers in bioengineering and biotechnology · 2023
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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

8 authors at 2 institutions in 1 country.

Peter GenoveseProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Anjali PatelProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Natalia ZiemkiewiczProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Allison PaoliProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Joseph BrunsProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Natasha CaseProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Silviya P ZustiakProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Koyal GargProgram of Biomedical Engineering, School of Engineering, Saint Louis University, St. Louis, Missouri, USA.
Saint Louis University · USUniversity of Missouri–St. Louis · US

Funding

Proregenerative Immunotherapies for Volumetric Muscle LossR15GM129731 · NIGMS · SAINT LOUIS UNIVERSITY · PI GARG, KOYAL · 2018 to 2024
$913k
Department of DefenseNational Institute of Health (NIGMS) 1R15GM129731NIGMS NIH HHS R15 GM129731
6 · The paper itself

Abstract

Volumetric muscle loss (VML) is traumatic or surgical loss of skeletal muscle with resultant functional impairment. Skeletal muscle's innate capacity for regeneration is lost with VML due to a critical loss of stem cells, extracellular matrix, and neuromuscular junctions. Consequences of VML include permanent disability or delayed amputations of the affected limb. Currently, a successful clinical therapy has not been identified. Mesenchymal stem cells (MSCs) possess regenerative and immunomodulatory properties and their three-dimensional aggregation can further enhance therapeutic efficacy. In this study, MSC aggregation into spheroids was optimized in vitro based on cellular viability, spheroid size, and trophic factor secretion. The regenerative potential of the optimized MSC spheroid therapy was then investigated in a murine model of VML injury. Experimental groups included an untreated VML injury control, intramuscular injection of MSC spheroids, and MSC spheroids encapsulated in a fibrin-laminin hydrogel. Compared to the untreated VML group, the spheroid encapsulating hydrogel group enhanced myogenic marker (i.e., MyoD and myogenin) protein expression, improved muscle mass, increased presence of centrally nucleated myofibers as well as small fibers (<500 μm

Indexed as

Cells, ImmobilizedMesenchymal Stem Cell TransplantationMuscle, SkeletalRegenerationSpheroids, CellularWounds and InjuriesAnimalsFibrinHydrogelsLamininMaleMesenchymal Stem CellsMiceFibrinHydrogelsLamininextracellular matrixhydrogelsvolumetric muscle loss

Identifiers

PMID34551191
PMCPMC8648985
OpenAlexW3201297381

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.