Evidence map›Paper›PMID 38003460›Full record

ArticleInternational journal of molecular sciences2023

Neural Marker Expression in Adipose-Derived Stem Cells Grown in PEG-Based 3D Matrix Is Enhanced in the Presence of B27 and CultureOne Supplements.

Neus Gomila Pelegri, Aleksandra M Stanczak, Amy L Bottomley, Max L Cummins, Bruce K Milthorpe, Catherine A Gorrie, Matthew P Padula, Jerran Santos

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

8 authors.

Neus Gomila PelegriAdvanced Tissue Engineering and Stem Cell Biology Group, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Aleksandra M StanczakSchool of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Amy L BottomleyMicrobial Imaging Facility, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Max L CumminsAustralian Institute for Microbiology and Infection, University of Technology Sydney, Ultimo, NSW 2007, Australia.ORCID 0000-0001-9333-7160
Bruce K MilthorpeAdvanced Tissue Engineering and Stem Cell Biology Group, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.ORCID 0000-0002-0867-9586
Catherine A GorrieNeural Injury Research Unit, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.ORCID 0000-0001-5934-2492
Matthew P PadulaSchool of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.ORCID 0000-0002-8283-0643
Jerran SantosAdvanced Tissue Engineering and Stem Cell Biology Group, School of Life Sciences, University of Technology Sydney, Ultimo, NSW 2007, Australia.ORCID 0000-0003-4067-220X

Funding

Schwartz Foundation SF-0001-2020
6 · The paper itself

Abstract

Adipose-derived stem cells (ADSCs) have incredible potential as an avenue to better understand and treat neurological disorders. While they have been successfully differentiated into neural stem cells and neurons, most such protocols involve 2D environments, which are not representative of in vivo physiology. In this study, human ADSCs were cultured in 1.1 kPa polyethylene-glycol 3D hydrogels for 10 days with B27, CultureOne (C1), and N2 neural supplements to examine the neural differentiation potential of ADSCs using both chemical and mechanical cues. Following treatment, cell viability, proliferation, morphology, and proteome changes were assessed. Results showed that cell viability was maintained during treatments, and while cells continued to proliferate over time, proliferation slowed down. Morphological changes between 3D untreated cells and treated cells were not observed. However, they were observed among 2D treatments, which exhibited cellular elongation and co-alignment. Proteome analysis showed changes consistent with early neural differentiation for B27 and C1 but not N2. No significant changes were detected using immunocytochemistry, potentially indicating a greater differentiation period was required. In conclusion, treatment of 3D-cultured ADSCs in PEG-based hydrogels with B27 and C1 further enhances neural marker expression, however, this was not observed using supplementation with N2.

Indexed as

Neural Stem CellsProteomeAdipose TissueBiocompatible MaterialsCell DifferentiationCells, CulturedHumansHydrogelsBiocompatible MaterialsHydrogelsProteome3D tissue culturebioprintingimmunocytochemistryneural developmentneural differentiationneuroregenerationpolyethylene glycolproteomicsregenerative medicinetissue engineering

Identifiers

PMID38003460
PMCPMC10671562

What OpenQuestion holds

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LicenceCC BY
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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.