Evidence map›Paper›PMID 20857388›Full record

ArticleMacromolecular bioscience2010

Multifunctional hybrid three-dimensionally woven scaffolds for cartilage tissue engineering.

Franklin T Moutos, Bradley T Estes, Farshid Guilak

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
  2. Article
  3. Functional tissue engineering of articular cartilage for biological joint resurfacing-The 2021 Elizabeth Winston Lanier Kappa Delta Award.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2022
    Article
  4. Article
  5. Review
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  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Anatomically shaped tissue-engineered cartilage with tunable and inducible anticytokine delivery for biological joint resurfacing.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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

3 authors.

Franklin T MoutosDepartments of Orthopaedic Surgery and Biomedical Engineering, Duke University Medical Center, 375 MSRB, Box 3093, Durham, NC 27710, USA.
Bradley T Estes
Farshid Guilak

Funding

Pilot Project for the DTMI CRA ProgramUL1RR024128 · NCRR · DUKE UNIVERSITY · PI CALIFF, ROBERT M · 2006 to 2010
$48.1M
Thermally-Triggered Intra-articular Drug Delivery for OAP01AR050245 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2012
$11.5M
VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONSR01AG015768 · NIA · WASHINGTON UNIVERSITY · PI GUILAK, FARSHID · 1998 to 2022
$7.7M
Mechanical and Osmotic Signaling in ChondrocytesR01AR048182 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2013
$3.0M
Intrinsic Repair of the Knee MeniscusR01AR048852 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2007 to 2011
$1.4M
Functional Tissue Engineering for Cartilage RepairR42AR055042 · NIAMS · CYTEX THERAPEUTICS INC. · PI GUILAK, FARSHID · 2013 to 2014
$1.3M
Functional Tissue Engineering for Cartilage RepairR41AR055042 · NIAMS · CYTEX THERAPEUTICS INC. · PI GUILAK, FARSHID · 2009 to 2009
$262k
Hybrid Composite Scaffolds for Cartilage Tissue EngineeringR43AR057600 · NIAMS · CYTEX THERAPEUTICS INC. · PI ERICKSON, GEOFFREY R · 2009 to 2009
$199k
NCRR NIH HHS RR024128NCRR NIH HHS UL1 RR024128NIAMS NIH HHS AR48182NIAMS NIH HHS AR48852NIAMS NIH HHS AR50245NIAMS NIH HHS AR55042NIAMS NIH HHS AR57600NIAMS NIH HHS P01 AR050245NIAMS NIH HHS R01 AR048182NIAMS NIH HHS R01 AR048852NIAMS NIH HHS R41 AR055042NIAMS NIH HHS R42 AR055042NIAMS NIH HHS R43 AR057600NIA NIH HHS AG15768NIA NIH HHS R01 AG015768
6 · The paper itself

Abstract

The successful replacement of large-scale cartilage defects or osteoarthritic lesions using tissue-engineering approaches will likely require composite biomaterial scaffolds that have biomimetic mechanical properties and can provide cell-instructive cues to control the growth and differentiation of embedded stem or progenitor cells. This study describes a novel method of constructing multifunctional scaffolds for cartilage tissue engineering that can provide both mechanical support and biological stimulation to seeded progenitor cells. 3-D woven PCL scaffolds were infiltrated with a slurry of homogenized CDM of porcine origin, seeded with human ASCs, and cultured for up to 42 d under standard growth conditions. These constructs were compared to scaffolds derived solely from CDM as well as 3-D woven PCL fabric without CDM. While all scaffolds promoted a chondrogenic phenotype of the ASCs, CDM scaffolds showed low compressive and shear moduli and contracted significantly during culture. Fiber-reinforced CDM scaffolds and 3-D woven PCL scaffolds maintained their mechanical properties throughout the culture period, while supporting the accumulation of a cartilaginous extracellular matrix. These findings show that fiber-reinforced hybrid scaffolds can be produced with biomimetic mechanical properties as well as the ability to promote ASC differentiation and chondrogenesis in vitro.

Indexed as

CartilageAdipose Tissue, WhiteAdultAdult Stem CellsAnimalsBiomechanical PhenomenaCell DifferentiationChondrocytesChondroitin SulfatesCollagenCollagen Type ICollagen Type IICompressive StrengthDNAElastic ModulusExtracellular MatrixA73025Chondroitin SulfatesCollagenCollagen Type ICollagen Type IIDNAGlycosaminoglycanspolycaprolactonePolyesters

Identifiers

PMID20857388
PMCPMC3214627

What OpenQuestion holds

Textmetadata
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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.