Evidence map›Paper›PMID 26895780›Full record

ArticleJournal of biomechanics2016

A puzzle assembly strategy for fabrication of large engineered cartilage tissue constructs.

Adam B Nover, Brian K Jones, William T Yu, Daniel S Donovan, Jeremy D Podolnick, James L Cook, Gerard A Ateshian, Clark T Hung

Abstract read
In one paragraph

Article in Journal of biomechanics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Decellularized Hydrogels in Bone Tissue Engineering: A Topical Review.International journal of medical sciences · 2018
    Review
  5. Review
  6. Article
  7. 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.

Adam B NoverDepartment of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, Mail Code: 8904, New York, NY 10027, USA. Electronic address: abn2106@columbia.edu.
Brian K JonesDepartment of Mechanical Engineering, Columbia University, 242 S. W. Mudd, 500 West 120th Street, Mail Code: 4703, New York, NY 10027, USA. Electronic address: bkj2106@columbia.edu.
William T YuDepartment of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, Mail Code: 8904, New York, NY 10027, USA. Electronic address: wty2102@columbia.edu.
Daniel S DonovanDepartment of Orthopedic Surgery, Mount Sinai West, 1000 Tenth Avenue, New York, NY 10019, USA; Department of Orthopedic Surgery, Mount Sinai St. Luke׳s, 1111 Amsterdam Avenue, New York, NY 10025, USA. Electronic address: dandonovan@chpnet.org.
Jeremy D PodolnickDepartment of Orthopedic Surgery, Mount Sinai West, 1000 Tenth Avenue, New York, NY 10019, USA; Department of Orthopedic Surgery, Mount Sinai St. Luke׳s, 1111 Amsterdam Avenue, New York, NY 10025, USA. Electronic address: jpodolnick@chpnet.org.
James L CookDepartment of Orthopaedic Surgery, University of Missouri, 1100 Virginia Avenue, DC953.000, Columbia, MO 65212, USA. Electronic address: CookJL@missouri.edu.
Gerard A AteshianDepartment of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, Mail Code: 8904, New York, NY 10027, USA; Department of Mechanical Engineering, Columbia University, 242 S. W. Mudd, 500 West 120th Street, Mail Code: 4703, New York, NY 10027, USA. Electronic address: ateshian@columbia.edu.
Clark T HungDepartment of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, Mail Code: 8904, New York, NY 10027, USA. Electronic address: cth6@columbia.edu.

Funding

Optimizing Nutrient Supply in Large Engineered Cartilage Tissue ConstructsR01AR060361 · NIAMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ATESHIAN, GERARD A., HUNG, CLARK T. · 2010 to 2014
$1.7M
NIAMS NIH HHS 1R01AR060361NIAMS NIH HHS R01 AR060361
6 · The paper itself

Abstract

Engineering of large articular cartilage tissue constructs remains a challenge as tissue growth is limited by nutrient diffusion. Here, a novel strategy is investigated, generating large constructs through the assembly of individually cultured, interlocking, smaller puzzle-shaped subunits. These constructs can be engineered consistently with more desirable mechanical and biochemical properties than larger constructs (~4-fold greater Young׳s modulus). A failure testing technique was developed to evaluate the physiologic functionality of constructs, which were cultured as individual subunits for 28 days, then assembled and cultured for an additional 21-35 days. Assembled puzzle constructs withstood large deformations (40-50% compressive strain) prior to failure. Their ability to withstand physiologic loads may be enhanced by increases in subunit strength and assembled culture time. A nude mouse model was utilized to show biocompatibility and fusion of assembled puzzle pieces in vivo. Overall, the technique offers a novel, effective approach to scaling up engineered tissues and may be combined with other techniques and/or applied to the engineering of other tissues. Future studies will aim to optimize this system in an effort to engineer and integrate robust subunits to fill large defects.

Indexed as

Mechanical PhenomenaAnimalsCartilage, ArticularCell Culture TechniquesChondrocytesElastic ModulusMiceTissue EngineeringArticular cartilageNutrient limitationsPuzzleScaling upTissue engineering

Identifiers

PMID26895780
PMCPMC4907770

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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.