Evidence map›Paper›PMID 39314156›Full record

ArticleScience progress

Incorporation of decellularized-ECM in graphene-based scaffolds enhances axonal outgrowth and branching in neuro-muscular co-cultures.

Carlos Serna, Kirtana Sandepudi, Rebecca L Keate, Sophia L Zhang, Kristen Y Cotton, Alberto De La Isla, Matias Murillo, Yasmine Bouricha, Andrea A Domenighetti, Colin K Franz and 1 more

Abstract read
In one paragraph

Article in Science progress. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Carlos SernaDivision of Plastic Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Kirtana SandepudiDivision of Plastic Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0009-0008-7981-4424
Rebecca L KeateSimpson Querrey Institute, Northwestern University, Chicago, IL, USA.
Sophia L ZhangDivision of Plastic Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Kristen Y CottonBiologics Laboratory, Shirley Ryan AbilityLab, Chicago, IL, USA.
Alberto De La IslaDivision of Plastic Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0000-0001-6070-0699
Matias MurilloBiologics Laboratory, Shirley Ryan AbilityLab, Chicago, IL, USA.
Yasmine BourichaBiologics Laboratory, Shirley Ryan AbilityLab, Chicago, IL, USA.
Andrea A DomenighettiBiologics Laboratory, Shirley Ryan AbilityLab, Chicago, IL, USA.
Colin K FranzBiologics Laboratory, Shirley Ryan AbilityLab, Chicago, IL, USA.
Sumanas W JordanDivision of Plastic Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Developing Capacity to Evaluate Training Programs via Development of Human, Institutional and Social CapitalT32GM008449 · NIGMS · NORTHWESTERN UNIVERSITY · PI LEONARD, JOSHUA NATHANIEL · 1993 to 2023
$7.8M
NCI NIH HHS P30 CA091842NIGMS NIH HHS T32 GM008449
6 · The paper itself

Abstract

Peripheral nerve and large-scale muscle injuries result in significant disability, necessitating the development of biomaterials that can restore functional deficits by promoting tissue regrowth in an electroactive environment. Among these materials, graphene is favored for its high conductivity, but its low bioactivity requires enhancement through biomimetic components. In this study, we extrusion printed graphene-poly(lactide-co-glycolide) (graphene) lattice scaffolds, aiming to increase bioactivity by incorporating decellularized extracellular matrix (dECM) derived from mouse pup skeletal muscle. We first evaluated these scaffolds using human-induced pluripotent stem cell (hiPSC)-derived motor neurons co-cultured with supportive glia, observing significant improvements in axon outgrowth. Next, we tested the scaffolds with C2C12 mouse and human primary myoblasts, finding no significant differences in myotube formation between dECM-graphene and graphene scaffolds. Finally, using a more complex hiPSC-derived 3D motor neuron spheroid model co-cultured with human myoblasts, we demonstrated that dECM-graphene scaffolds significantly improved axonal expansion towards peripheral myoblasts and increased axonal network density compared to graphene-only scaffolds. Features of early neuromuscular junction formation were identified near neuromuscular interfaces in both scaffold types. These findings suggest that dECM-graphene scaffolds are promising candidates for enhancing neuromuscular regeneration, offering robust support for the growth and development of diverse neuromuscular tissues.

Indexed as

Coculture TechniquesExtracellular MatrixGraphiteInduced Pluripotent Stem CellsTissue ScaffoldsAnimalsAxonsCell DifferentiationHumansMiceMotor NeuronsMuscle, SkeletalMyoblastsNeuromuscular JunctionNeuronal OutgrowthTissue EngineeringGraphiteco-cultureextracellular matrixGrapheneneuromuscular regeneration

Identifiers

PMID39314156
PMCPMC11423365

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.