Evidence map›Paper›PMID 26219862›Full record

ReviewActa biomaterialia2015

Biomimetic scaffolds for regeneration of volumetric muscle loss in skeletal muscle injuries.

Jonathan M Grasman, Michelle J Zayas, Raymond L Page, George D Pins

Abstract readReview
In one paragraph

Review in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

116 citing papers in PubMed, 241 citations in OpenAlex.

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  13. Aligned Collagen Sponges Loaded With Myogenic Factors to Enhance Skeletal Muscle Tissue Regeneration.Journal of biomedical materials research. Part B, Applied biomaterials · 2025
    Article
  14. Review
  15. A novel protocol for the direct isolation of a highly pure and regenerative population of satellite stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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56 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 1 institution in 1 country.

Jonathan M GrasmanBiomedical Engineering Department, Worcester Polytechnic Institute, Worcester, MA 01609, United States; Bioengineering Institute, Worcester Polytechnic Institute, Worcester, MA 01609, United States.
Michelle J ZayasBiomedical Engineering Department, Worcester Polytechnic Institute, Worcester, MA 01609, United States.
Raymond L PageBiomedical Engineering Department, Worcester Polytechnic Institute, Worcester, MA 01609, United States; Bioengineering Institute, Worcester Polytechnic Institute, Worcester, MA 01609, United States.
George D PinsBiomedical Engineering Department, Worcester Polytechnic Institute, Worcester, MA 01609, United States; Bioengineering Institute, Worcester Polytechnic Institute, Worcester, MA 01609, United States. Electronic address: gpins@wpi.edu.
Worcester Polytechnic Institute · US

Funding

Biological sutures to enhance progenitor cell delivery and retention in the heartR01HL115282 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI GAUDETTE, GLENN R · 2013 to 2017
$1.9M
Designing Fibrin Microthread Scaffolds for Skeletal Muscle RegenerationF31DE023281 · NIDCR · WORCESTER POLYTECHNIC INSTITUTE · PI GRASMAN, JONATHAN M. · 2013 to 2014
$61k
NHLBI NIH HHS R01 HL115282NHLBI NIH HHS R01-HL115282NIDCR NIH HHS F31 DE023281NIDCR NIH HHS F31-DE023281
6 · The paper itself

Abstract

Skeletal muscle injuries typically result from traumatic incidents such as combat injuries where soft-tissue extremity injuries are present in one of four cases. Further, about 4.5 million reconstructive surgical procedures are performed annually as a result of car accidents, cancer ablation, or cosmetic procedures. These combat- and trauma-induced skeletal muscle injuries are characterized by volumetric muscle loss (VML), which significantly reduces the functionality of the injured muscle. While skeletal muscle has an innate repair mechanism, it is unable to compensate for VML injuries because large amounts of tissue including connective tissue and basement membrane are removed or destroyed. This results in a significant need to develop off-the-shelf biomimetic scaffolds to direct skeletal muscle regeneration. Here, the structure and organization of native skeletal muscle tissue is described in order to reveal clear design parameters that are necessary for scaffolds to mimic in order to successfully regenerate muscular tissue. We review the literature with respect to the materials and methodologies used to develop scaffolds for skeletal muscle tissue regeneration as well as the limitations of these materials. We further discuss the variety of cell sources and different injury models to provide some context for the multiple approaches used to evaluate these scaffold materials. Recent findings are highlighted to address the state of the field and directions are outlined for future strategies, both in scaffold design and in the use of different injury models to evaluate these materials, for regenerating functional skeletal muscle. STATEMENT OF SIGNIFICANCE: Volumetric muscle loss (VML) injuries result from traumatic incidents such as those presented from combat missions, where soft-tissue extremity injuries are represented in one of four cases. These injuries remove or destroy large amounts of skeletal muscle including the basement membrane and connective tissue, removing the structural, mechanical, and biochemical cues that usually direct its repair. This results in a significant need to develop off-the-shelf biomimetic scaffolds to direct skeletal muscle regeneration. In this review, we examine current strategies for the development of scaffold materials designed for skeletal muscle regeneration, highlighting advances and limitations associated with these methodologies. Finally, we identify future approaches to enhance skeletal muscle regeneration.

Indexed as

AnimalsBiomimetic MaterialsDisease Models, AnimalHumansMuscle, SkeletalRegenerationTissue EngineeringTissue ScaffoldsBiomaterialsFibrinMicrothreadsSkeletal muscle regenerationTissue engineering

Identifiers

PMID26219862
PMCPMC4562809
OpenAlexW1007294394

What OpenQuestion 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 OpenQuestion graph.