Evidence map›Paper›PMID 32541821›Full record

ArticleNature communications2020

Characterization of a pluripotent stem cell-derived matrix with powerful osteoregenerative capabilities.

Eoin P McNeill, Suzanne Zeitouni, Simin Pan, Andrew Haskell, Michael Cesarek, Daniel Tahan, Bret H Clough, Ulf Krause, Lauren K Dobson, Mayra Garcia and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Immune escape ofFrontiers in cellular and infection microbiology · 2025
    Review
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  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Science advances · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

16 authors.

Eoin P McNeillDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Suzanne ZeitouniDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Simin PanDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Andrew HaskellDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.ORCID http://orcid.org/0000-0003-1170-2254
Michael CesarekDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.ORCID http://orcid.org/0000-0003-0931-5941
Daniel TahanDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Bret H CloughDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Ulf KrauseInstitute for Transfusion Medicine and Cellular Medicine, University Hospital Muenster, Muenster, Germany.ORCID http://orcid.org/0000-0002-8965-2114
Lauren K DobsonDepartment of Small Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, 77843, USA.
Mayra GarciaDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Christopher KungDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.ORCID http://orcid.org/0000-0002-0588-121X
Qingguo ZhaoDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
W Brian SaundersDepartment of Small Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, 77843, USA.
Fei LiuDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Roland KaunasDepartment of Biomedical Engineering, Texas A&M University, College Station, TX, 77843, USA. kaunas@tamu.edu.
Carl A GregoryDepartment of Molecular and Cellular Medicine, Institute for Regenerative Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA. cgregory@tamu.edu.

Funding

Advanced Methods for Mimicking the Osteogenic Niche to Heal BoneR01AR066033 · NIAMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GREGORY, CARL A. · 2014 to 2017
$1.3M
Nanoengineered bone repair scaffolds generated from stem cells and their secreted products for improved spinal fusionR21AR072292 · NIAMS · TEXAS A&M UNIVERSITY · PI GREGORY, CARL A. · 2019 to 2020
$349k
NIAMS NIH HHS R01 AR066033NIAMS NIH HHS R21 AR072292
6 · The paper itself

Abstract

Approximately 10% of fractures will not heal without intervention. Current treatments can be marginally effective, costly, and some have adverse effects. A safe and manufacturable mimic of anabolic bone is the primary goal of bone engineering, but achieving this is challenging. Mesenchymal stem cells (MSCs), are excellent candidates for engineering bone, but lack reproducibility due to donor source and culture methodology. The need for a bioactive attachment substrate also hinders progress. Herein, we describe a highly osteogenic MSC line generated from induced pluripotent stem cells that generates high yields of an osteogenic cell-matrix (ihOCM) in vitro. In mice, the intrinsic osteogenic activity of ihOCM surpasses bone morphogenic protein 2 (BMP2) driving healing of calvarial defects in 4 weeks by a mechanism mediated in part by collagen VI and XII. We propose that ihOCM may represent an effective replacement for autograft and BMP products used commonly in bone tissue engineering.

Indexed as

OsteogenesisAnimalsBone Morphogenetic Protein 2Cell ProliferationCells, CulturedCollagen Type VICollagen Type XIICraniofacial AbnormalitiesHumansMesenchymal Stem CellsMicePluripotent Stem CellsTissue EngineeringBone Morphogenetic Protein 2Collagen Type VICollagen Type XII

Identifiers

PMID32541821
PMCPMC7295745

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.