Evidence map›Paper›PMID 29273221›Full record

ArticleJournal of biomechanics2018

A modular approach to creating large engineered cartilage surfaces.

Audrey C Ford, Wan Fung Chui, Anne Y Zeng, Aditya Nandy, Ellen Liebenberg, Carlo Carraro, Galateia Kazakia, Tamara Alliston, Grace D O'Connell

Abstract read
In one paragraph

Article in Journal of biomechanics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors.

Audrey C FordDepartment of Mechanical Engineering, University of California, Berkeley, United States.
Wan Fung ChuiDepartment of Mechanical Engineering, University of California, Berkeley, United States.
Anne Y ZengDepartment of Mechanical Engineering, University of California, Berkeley, United States.
Aditya NandyDepartment of Mechanical Engineering, University of California, Berkeley, United States.
Ellen LiebenbergDepartment of Orthopaedic Surgery, University of California, San Francisco, United States.
Carlo CarraroDepartment of Chemical Engineering, University of California, Berkeley, United States.
Galateia KazakiaDepartment of Radiology, University of California, San Francisco, United States.
Tamara AllistonDepartment of Orthopaedic Surgery, University of California, San Francisco, United States.
Grace D O'ConnellDepartment of Mechanical Engineering, University of California, Berkeley, United States. Electronic address: g.oconnell@berkeley.edu.

Funding

The mechanistic control of bone quality and joint crosstalk by osteocytesR01DE019284 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, CHRISTOPHER JOHN · 2009 to 2024
$7.6M
UCSF Core Center for Musculoskeletal Biology and MedicineP30AR066262 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MAJUMDAR, SHARMILA · 2014 to 2018
$3.0M
The mechanobiology of TGF-beta signaling in chondrocytesR21AR067439 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALLISTON, TAMARA N · 2014 to 2015
$407k
NIAMS NIH HHS P30 AR066262NIAMS NIH HHS R21 AR067439NIDCR NIH HHS R01 DE019284
6 · The paper itself

Abstract

Native articular cartilage has limited capacity to repair itself from focal defects or osteoarthritis. Tissue engineering has provided a promising biological treatment strategy that is currently being evaluated in clinical trials. However, current approaches in translating these techniques to developing large engineered tissues remains a significant challenge. In this study, we present a method for developing large-scale engineered cartilage surfaces through modular fabrication. Modular Engineered Tissue Surfaces (METS) uses the well-known, but largely under-utilized self-adhesion properties of de novo tissue to create large scaffolds with nutrient channels. Compressive mechanical properties were evaluated throughout METS specimens, and the tensile mechanical strength of the bonds between attached constructs was evaluated over time. Raman spectroscopy, biochemical assays, and histology were performed to investigate matrix distribution. Results showed that by Day 14, stable connections had formed between the constructs in the METS samples. By Day 21, bonds were robust enough to form a rigid sheet and continued to increase in size and strength over time. Compressive mechanical properties and glycosaminoglycan (GAG) content of METS and individual constructs increased significantly over time. The METS technique builds on established tissue engineering accomplishments of developing constructs with GAG composition and compressive properties approaching native cartilage. This study demonstrated that modular fabrication is a viable technique for creating large-scale engineered cartilage, which can be broadly applied to many tissue engineering applications and construct geometries.

Indexed as

AnimalsCartilage, ArticularCompressive StrengthGlycosaminoglycansStress, MechanicalSurface PropertiesTensile StrengthTissue EngineeringGlycosaminoglycansArticular cartilageModular fabricationTissue engineering

Identifiers

PMID29273221
PMCPMC5767151

What Socratic 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 Socratic graph.