Evidence map›Paper›PMID 26524412›Full record

ArticleOsteoarthritis and cartilage2016

Acid ceramidase treatment enhances the outcome of autologous chondrocyte implantation in a rat osteochondral defect model.

M E Frohbergh, J M Guevara, R P Grelsamer, M F Barbe, X He, C M Simonaro, E H Schuchman

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Article in Osteoarthritis and cartilage, 2016. 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
2.1field-weighted citation impact, top 13% of its field
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, 14 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

M E FrohberghDepartment of Genetics and Genomic Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J M GuevaraInstitute for the Study of Inborn Errors of Metabolism, Pontificia Universidad Javeriana, Bogota, Colombia.
R P GrelsamerDepartment of Orthopedic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
M F BarbeDepartment of Anatomy and Cell Biology, Temple University, Philadelphia, PA, USA.
X HeDepartment of Genetics and Genomic Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
C M SimonaroDepartment of Genetics and Genomic Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
E H SchuchmanDepartment of Genetics and Genomic Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: Edward.schuchman@mssm.edu.
Icahn School of Medicine at Mount Sinai · USPontificia Universidad Javeriana · COTemple University · US

Funding

CERAMIDASES, CERAMIDE, AND FARBER DISEASER01DK054830 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHUCHMAN, EDWARD H. · 2000 to 2015
$5.3M
NIDDK NIH HHS R01 DK054830NIDDK NIH HHS R01 DK54830
6 · The paper itself

Abstract

objectiveThe overall aim of this study was to evaluate how supplementation of chondrocyte media with recombinant acid ceramidase (rhAC) influenced cartilage repair in a rat osteochondral defect model.

methodsPrimary chondrocytes were grown as monolayers in polystyrene culture dishes with and without rhAC (added once at the time of cell plating) for 7 days, and then seeded onto Bio-Gide® collagen scaffolds and grown for an additional 3 days. The scaffolds were then introduced into osteochondral defects created in Sprague-Dawley rat trochlea by a microdrilling procedure. Analysis was performed 6 weeks post-surgery macroscopically, by micro-CT, histologically, and by immunohistochemistry.

resultsTreatment with rhAC led to increased cell numbers and glycosaminoglycan (GAG) production (∼2 and 3-fold, respectively) following 7 days of expansion in vitro. Gene expression of collagen 2, aggrecan and Sox-9 also was significantly elevated. After seeding onto Bio-Gide®, more rhAC treated cells were evident within 4 h. At 6 weeks post-surgery, defects containing rhAC-treated cells exhibited more soft tissue formation at the articular surface, as evidenced by microCT, as well as histological evidence of enhanced cartilage repair. Notably, collagen 2 immunostaining revealed greater surface expression in animals receiving rhAC treated cells as well. Collagen 10 staining was not enhanced.

conclusionThe results further demonstrate the positive effects of rhAC treatment on chondrocyte growth and phenotype in vitro, and reveal for the first time the in vivo effects of the treated cells on cartilage repair.

Indexed as

Acid CeramidaseAnimalsCartilage, ArticularCell CountCells, CulturedChondrocytesCulture Media, ConditionedDrug Evaluation, PreclinicalFemaleGlycosaminoglycansRats, Sprague-DawleyRecombinant ProteinsRegenerationTissue ScaffoldsWound HealingX-Ray MicrotomographyAcid CeramidaseCulture Media, ConditionedGlycosaminoglycansRecombinant ProteinsAcid ceramidaseAutologous chondrocyte implantation (ACI)Cartilage tissue engineeringIn vivoOsteochondral defect modelPrimary chondrocyte expansion

Identifiers

PMID26524412
PMCPMC4799741
OpenAlexW2146980384

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.