Evidence map›Paper›PMID 35762455›Full record

ArticleJournal of biomedical materials research. Part A2022

Controlling scaffold conductivity and pore size to direct myogenic cell alignment and differentiation.

Ivan M Basurto, Samir A Muhammad, Gregg M Gardner, George J Christ, Steven R Caliari

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Edible Sulfonated Soy Protein Microcarriers for Cultivated Meat Cell Expansion.Journal of biomedical materials research. Part A · 2026
    Article
  4. Article
  5. Review
  6. Heparin-Modified Aligned Collagen Scaffolds Enhance In Vitro Myogenesis.Journal of biomedical materials research. Part A · 2026
    Article
  7. Edible Scaffolds for Cultivated Meat Production.Advances in biochemical engineering/biotechnology · 2026
    Review
  8. Heparin-modified aligned collagen scaffolds enhancebioRxiv : the preprint server for biology · 2025
    Article
  9. Aligned Collagen Sponges Loaded With Myogenic Factors to Enhance Skeletal Muscle Tissue Regeneration.Journal of biomedical materials research. Part B, Applied biomaterials · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Skeletal Muscle Tissue Engineering: From Tissue Regeneration to Biorobotics.Cyborg and bionic systems (Washington, D.C.) · 2025
    Review
  14. Tuning porosity of macroporous hydrogels enables rapid rates of stress relaxation and promotes cell expansion and migration.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

5 authors at 1 institution in 1 country.

Ivan M BasurtoDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.
Samir A MuhammadDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.
Gregg M GardnerDepartment of Chemical Engineering, University of Virginia, Charlottesville, Virginia, USA.
George J ChristDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.
Steven R CaliariDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0002-7506-3079
University of Virginia · US

Funding

Biotechnology Training ProgramT32GM136615 · NIGMS · UNIVERSITY OF VIRGINIA · PI Silvia Salinas Blemker, Kimberly A. Kelly · 2020 to 2026
$3.4M
Aligned and electrically conductive collagen scaffolds for guiding innervated muscle-tendon junction repair of volumetric muscle loss injuriesR01AR078866 · NIAMS · UNIVERSITY OF VIRGINIA · PI CALIARI, STEVEN · 2021 to 2025
$2.0M
Using Molecular Modeling to Determine Structure and Organization in Skin LipidsR01AR057886 · NIAMS · VANDERBILT UNIVERSITY · PI MCCABE, CLARE · 2010 to 2012
$601k
Aligned and Conductive 3D Collagen Scaffolds for Skeletal Muscle Tissue EngineeringR21AR075181 · NIAMS · UNIVERSITY OF VIRGINIA · PI CALIARI, STEVEN · 2019 to 2020
$356k
NIAMS NIH HHS R01 AR057886NIAMS NIH HHS R01 AR078866NIAMS NIH HHS R21 AR075181NIGMS NIH HHS T32 GM136615
6 · The paper itself

Abstract

Skeletal muscle's combination of three-dimensional (3D) anisotropy and electrical excitability is critical for enabling normal movement. We previously developed a 3D aligned collagen scaffold incorporating conductive polypyrrole (PPy) particles to recapitulate these key muscle properties and showed that the scaffold facilitated enhanced myotube maturation compared with nonconductive controls. To further optimize this scaffold design, this work assessed the influence of conductive polymer incorporation and scaffold pore architecture on myogenic cell behavior. Conductive PPy and poly(3,4-ethylenedioxythiophene) (PEDOT) particles were synthesized and mixed into a suspension of type I collagen and chondroitin sulfate prior to directional freeze-drying to produce anisotropic scaffolds. Energy dispersive spectroscopy revealed homogenous distribution of conductive PEDOT particles throughout the scaffolds that resulted in a threefold increase in electrical conductivity while supporting similar myoblast metabolic activity compared to nonconductive scaffolds. Control of freezing temperature enabled fabrication of PEDOT-doped scaffolds with a range of pore diameters from 98 to 238 μm. Myoblasts conformed to the anisotropic contact guidance cues independent of pore size to display longitudinal cytoskeletal alignment. The increased specific surface area of the smaller pore scaffolds helped rescue the initial decrease in myoblast metabolic activity observed in larger pore conductive scaffolds while also promoting modestly increased expression levels of the myogenic marker myosin heavy chain (MHC) and gene expression of myoblast determination protein (MyoD). However, cell infiltration to the center of the scaffolds was marginally reduced compared with larger pore variants. Together these data underscore the potential of aligned and PEDOT-doped collagen scaffolds for promoting myogenic cell organization and differentiation.

Indexed as

PolymersTissue ScaffoldsCell DifferentiationCollagenElectric ConductivityPyrrolesTissue EngineeringCollagenPolymersPyrroleselectrically conductivepore sizescaffoldskeletal muscle

Identifiers

PMID35762455
PMCPMC9540010
OpenAlexW4283652989

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.