Evidence map›Paper›PMID 26675008›Full record

ArticlePloS one2015

In Vivo Assessment of Bone Regeneration in Alginate/Bone ECM Hydrogels with Incorporated Skeletal Stem Cells and Single Growth Factors.

David Gothard, Emma L Smith, Janos M Kanczler, Cameron R Black, Julia A Wells, Carol A Roberts, Lisa J White, Omar Qutachi, Heather Peto, Hassan Rashidi and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  8. Mechanobiology in medicine · 2024
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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

16 authors at 4 institutions in 1 country.

David GothardBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Emma L SmithBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Janos M KanczlerBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Cameron R BlackBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Julia A WellsBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Carol A RobertsBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
Lisa J WhiteWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Omar QutachiWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Heather PetoWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Hassan RashidiWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Luis RojoDepartment of Materials, Imperial College London, Royal School of Mines, London, SW7 2AZ, United Kingdom.
Molly M StevensDepartment of Materials, Imperial College London, Royal School of Mines, London, SW7 2AZ, United Kingdom.
Alicia J El HajInstitute for Science and Technology in Medicine, Keele University, Guy Hilton Research Centre, Stoke-on-Trent, ST4 7BQ, United Kingdom.
Felicity R A J RoseWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Kevin M ShakesheffWolfson Centre for Stem Cells, Tissue Engineering and Modelling, School of Pharmacy, University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham, NG7 2RD, United Kingdom.
Richard O C OreffoBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton, SO16 6YD, United Kingdom.
University of Southampton · GBUniversity of Nottingham · GBImperial College London · GBKeele University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G010579/1Biotechnology and Biological Sciences Research Council BB/G010617/1
6 · The paper itself

Abstract

The current study has investigated the use of decellularised, demineralised bone extracellular matrix (ECM) hydrogel constructs for in vivo tissue mineralisation and bone formation. Stro-1-enriched human bone marrow stromal cells were incorporated together with select growth factors including VEGF, TGF-β3, BMP-2, PTHrP and VitD3, to augment bone formation, and mixed with alginate for structural support. Growth factors were delivered through fast (non-osteogenic factors) and slow (osteogenic factors) release PLGA microparticles. Constructs of 5 mm length were implanted in vivo for 28 days within mice. Dense tissue assessed by micro-CT correlated with histologically assessed mineralised bone formation in all constructs. Exogenous growth factor addition did not enhance bone formation further compared to alginate/bone ECM (ALG/ECM) hydrogels alone. UV irradiation reduced bone formation through degradation of intrinsic growth factors within the bone ECM component and possibly also ECM cross-linking. BMP-2 and VitD3 rescued osteogenic induction. ALG/ECM hydrogels appeared highly osteoinductive and delivery of angiogenic or chondrogenic growth factors led to altered bone formation. All constructs demonstrated extensive host tissue invasion and vascularisation aiding integration and implant longevity. The proposed hydrogel system functioned without the need for growth factor incorporation or an exogenous inducible cell source. Optimal growth factor concentrations and spatiotemporal release profiles require further assessment, as the bone ECM component may suffer batch variability between donor materials. In summary, ALG/ECM hydrogels provide a versatile biomaterial scaffold for utilisation within regenerative medicine which may be tailored, ultimately, to form the tissue of choice through incorporation of select growth factors.

Indexed as

Bone RegenerationExtracellular MatrixAlginatesAnimalsChondrogenesisGlucuronic AcidHexuronic AcidsHumansHydrogelsIntercellular Signaling Peptides and ProteinsLactic AcidMiceMiddle AgedOsteoblastsOsteogenesisPolyglycolic AcidAlginatesGlucuronic AcidHexuronic AcidsHydrogelsIntercellular Signaling Peptides and ProteinsLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymer

Identifiers

PMID26675008
PMCPMC4684226
OpenAlexW2215589249

What OpenQuestion holds

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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.