Evidence map›Paper›PMID 30985969›Full record

ArticleAnnals of the New York Academy of Sciences2019

Polymeric mesh and insulin-like growth factor 1 delivery enhance cell homing and graft-cartilage integration.

Margaret K Boushell, Christopher Z Mosher, Gurbani K Suri, Stephen B Doty, Eric J Strauss, Ernst B Hunziker, Helen H Lu

Abstract read
In one paragraph

Article in Annals of the New York Academy of Sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  11. Engineering collagenous analogs of connective tissue extracellular matrix.Frontiers in bioengineering and biotechnology · 2022
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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

7 authors.

Margaret K BoushellBiomaterials and Interface Tissue Engineering Laboratory, Department of Biomedical Engineering, Columbia University, New York, New York.
Christopher Z MosherAnalytical Microscopy Laboratory, Hospital for Special Surgery, New York, New York.
Gurbani K SuriBiomaterials and Interface Tissue Engineering Laboratory, Department of Biomedical Engineering, Columbia University, New York, New York.
Stephen B DotyAnalytical Microscopy Laboratory, Hospital for Special Surgery, New York, New York.
Eric J StraussDepartment of Orthopaedic Surgery, NYU Langone Medical Center, New York, New York.
Ernst B HunzikerDepartment of BioMedical Research, University Hospital of Bern, University of Bern, Bern, Switzerland.
Helen H LuBiomaterials and Interface Tissue Engineering Laboratory, Department of Biomedical Engineering, Columbia University, New York, New York.ORCID 0000-0002-9329-7290

Funding

Integrated Cartilage RepairR01AR073529 · NIAMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LU, HELEN H · 2018 to 2022
$1.8M
Multidisciplinary Engineering Training in Musculoskeletal ResearchT32AR059038 · NIAMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ATESHIAN, GERARD A. · 2011 to 2015
$1.3M
National Science Foundation DGE 16-44869New York State Stem Cell Science NYSTEMNIAMS NIH HHS R01 AR073529NIAMS NIH HHS T32 AR059038NIH HHS T32 AR059038
6 · The paper itself

Abstract

Cartilage injury, such as full-thickness lesions, predisposes patients to the premature development of osteoarthritis, a degenerative joint disease. While surgical management of cartilage lesions has improved, long-term clinical efficacy has stagnated, owing to the lack of hyaline cartilage regeneration and inadequate graft-host integration. This study tests the hypothesis that integration of cartilage grafts with native cartilage can be improved by enhancing the migration of chondrocytes across the graft-host interface via the release of chemotactic factor from a degradable polymeric mesh. To this end, a polylactide-co-glycolide/poly-ε-caprolactone mesh was designed to localize the delivery of insulin-like growth factor 1 (IGF-1), a well-established chondrocyte attractant. The release of IGF-1 (100 ng/mg) enhanced cell migration from cartilage explants, and the mesh served as critical structural support for cell adhesion, growth, and production of a cartilaginous matrix in vitro, which resulted in increased integration strength compared with mesh-free repair. Further, this neocartilage matrix was structurally contiguous with native and grafted cartilage when tested in an osteochondral explant model in vivo. These results demonstrate that this combined approach of a cell homing factor and supportive matrix will promote cell-mediated integrative cartilage repair and improve clinical outcomes of cartilage grafts in the treatment of osteoarthritis.

Indexed as

RegenerationAnimalsCartilage, ArticularCattleCell ProliferationCells, CulturedCell SurvivalChondrocytesInsulin-Like Growth Factor IPolymersInsulin-Like Growth Factor IPolymerscartilagechemotaxischondrocyteelectrospinningIGF-1interface

Identifiers

PMID30985969
PMCPMC7596880

What OpenQuestion holds

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Registered trials

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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.