Evidence map›Paper›PMID 32639692›Full record

ArticleStem cells translational medicine2020

Three-dimensional environment and vascularization induce osteogenic maturation of human adipose-derived stem cells comparable to that of bone-derived progenitors.

Amel Ibrahim, Naiara Rodriguez-Florez, Oliver F W Gardner, Eleonora Zucchelli, Sophie E P New, Alessandro Borghi, David Dunaway, Neil W Bulstrode, Patrizia Ferretti

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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

9 authors at 3 institutions in 2 countries.

Amel IbrahimStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0003-1102-721X
Naiara Rodriguez-FlorezStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
Oliver F W GardnerStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
Eleonora ZucchelliStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
Sophie E P NewStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
Alessandro BorghiStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
David DunawayStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.
Neil W BulstrodeDepartment of Plastic Surgery, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Patrizia FerrettiStem Cells and Regenerative Medicine Section, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-3590-6772
University College London · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBGreat Ormond Street Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While human adipose-derived stem cells (hADSCs) are known to possess osteogenic differentiation potential, the bone tissues formed are generally considered rudimentary and immature compared with those made by bone-derived precursor cells such as human bone marrow-derived mesenchymal stem cells (hBMSCs) and less commonly studied human calvarium osteoprogenitor cells (hOPs). Traditional differentiation protocols have tended to focus on osteoinduction of hADSCs through the addition of osteogenic differentiation media or use of stimulatory bioactive scaffolds which have not resulted in mature bone formation. Here, we tested the hypothesis that by reproducing the physical as well as biochemical bone microenvironment through the use of three-dimensional (3D) culture and vascularization we could enhance osteogenic maturation in hADSCs. In addition to biomolecular characterization, we performed structural analysis through extracellular collagen alignment and mineral density in our bone tissue engineered samples to evaluate osteogenic maturation. We further compared bone formed by hADSCs, hBMSCs, and hOPs against mature human pediatric calvarial bone, yet not extensively investigated. Although bone generated by all three cell types was still less mature than native pediatric bone, a fibrin-based 3D microenvironment together with vascularization boosted osteogenic maturation of hADSC making it similar to that of bone-derived osteoprogenitors. This demonstrates the important role of vascularization and 3D culture in driving osteogenic maturation of cells easily available but constitutively less committed to this lineage and suggests a crucial avenue for recreating the bone microenvironment for tissue engineering of mature craniofacial bone tissues from pediatric hADSCs, as well as hBMSCs and hOPs.

Indexed as

Adipose TissueHumansOsteogenesisStem CellsTissue EngineeringTissue Scaffolds3D environmentbonedifferentiationhuman adipose-derived stem cellsmesenchymal stem cellsosteogenesisprogenitor cellstissue engineeringvascularization

Identifiers

PMID32639692
PMCPMC7695642
OpenAlexW3041956933

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.