Evidence map›Paper›PMID 38562112›Full record

ArticleTissue engineering. Part C, Methods2024

Developing Porous Fibrin Scaffolds with Tunable Anisotropic Features to Direct Myoblast Orientation.

Bryanna L Samolyk, Zoe Y Pace, Juanyong Li, Kristen L Billiar, Jeannine M Coburn, Catherine F Whittington, George D Pins

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Edible Scaffolds for Cultivated Meat Production.Advances in biochemical engineering/biotechnology · 2026
    Review
  2. 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

7 authors at 1 institution in 1 country.

Bryanna L SamolykDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.ORCID 0000-0001-7619-8250
Zoe Y PaceDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.
Juanyong LiDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.
Kristen L BilliarDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.ORCID 0000-0002-4808-3939
Jeannine M CoburnDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.ORCID 0000-0001-6354-5436
Catherine F WhittingtonDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.ORCID 0000-0002-5821-4437
George D PinsDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts, USA.ORCID 0000-0002-8844-8074
Worcester Polytechnic Institute · US

Funding

American Heart Association-American Stroke Association 953260
6 · The paper itself

Abstract

Functional regeneration of anisotropically aligned tissues such as ligaments, microvascular networks, myocardium, or skeletal muscle requires a temporal and spatial series of biochemical and biophysical cues to direct cell functions that promote native tissue regeneration. When these cues are lost during traumatic injuries such as volumetric muscle loss (VML), scar formation occurs, limiting the regenerative capacity of the tissue. Currently, autologous tissue transfer is the gold standard for treating injuries such as VML but can result in adverse outcomes including graft failure, donor site morbidity, and excessive scarring. Tissue-engineered scaffolds composed of biomaterials, cells, or both have been investigated to promote functional tissue regeneration but are still limited by inadequate tissue ingrowth. These scaffolds should provide precisely tuned topographies and stiffnesses using proregenerative materials to encourage tissue-specific functions such as myoblast orientation, followed by aligned myotube formation and recovery of functional contraction. In this study, we describe the design and characterization of novel porous fibrin scaffolds with anisotropic microarchitectural features that recapitulate the native tissue microenvironment and offer a promising approach for regeneration of aligned tissues. We used directional freeze-casting with varied fibrin concentrations and freezing temperatures to produce scaffolds with tunable degrees of anisotropy and strut widths. Nanoindentation analyses showed that the moduli of our fibrin scaffolds varied as a function of fibrin concentration and were consistent with native skeletal muscle tissue. Quantitative morphometric analyses of myoblast cytoskeletons on scaffold microarchitectures demonstrated enhanced cell alignment as a function of microarchitectural morphology. The ability to precisely control the anisotropic features of fibrin scaffolds promises to provide a powerful tool for directing aligned tissue ingrowth and enhance functional regeneration of tissues such as skeletal muscle.

Indexed as

FibrinMyoblastsTissue ScaffoldsAnimalsAnisotropyCell LineMicePorosityTissue EngineeringFibrinanisotropyfibringuided cellular alignmentporous scaffoldskeletal muscletissue engineering

Identifiers

PMID38562112
PMCPMC11812604
OpenAlexW4393500691

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.