Effect of Mechanical Mincing on Minimally Manipulated Articular Cartilage for Surgical Transplantation.


Journal

The American journal of sports medicine
ISSN: 1552-3365
Titre abrégé: Am J Sports Med
Pays: United States
ID NLM: 7609541

Informations de publication

Date de publication:
07 2022
Historique:
pubmed: 24 6 2022
medline: 19 7 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

Point-of-care treatment options for medium to large symptomatic articular cartilage defects are limited. Minced cartilage implantation is an encouraging single-stage option, providing fresh viable autologous tissue with minimal morbidity and cost. To determine the histological properties of mechanically minced versus minimally manipulated articular cartilage. Controlled laboratory study. Remnant articular cartilage was collected from fresh femoral condylar allografts. Cartilage samples were divided into 4 groups: cartilage explants with or without fibrin glue and mechanically minced cartilage with or without fibrin glue. Samples were cultured for 42 days. Chondrocyte viability was assessed using live/dead assay. Cellular migration and outgrowth were monitored using bright-field microscopy. Extracellular matrix deposition was assessed via histological staining. Proteoglycan content and synthesis were assessed using dimethylmethylene blue assay and radiolabeled 35S-sulfate, respectively. Type II collagen (COL2A1) gene expression was analyzed via polymerase chain reaction. The mean viability of minced cartilage particles (34% ± 14%) was not significantly reduced compared with baseline (46% ± 13%) on day 0 ( Mechanically minced articular cartilage remained viable after 42 days of culture in vitro and was comparable with cartilage explants with regard to cellular migration, outgrowth, and extracellular matrix synthesis. Mechanically minced articular cartilage is an encouraging intervention for the treatment of symptomatic cartilage defects. Further translational work is warranted to determine the viability of minced cartilage implantation as a single-stage therapeutic intervention in vivo.

Sections du résumé

BACKGROUND
Point-of-care treatment options for medium to large symptomatic articular cartilage defects are limited. Minced cartilage implantation is an encouraging single-stage option, providing fresh viable autologous tissue with minimal morbidity and cost.
PURPOSE
To determine the histological properties of mechanically minced versus minimally manipulated articular cartilage.
STUDY DESIGN
Controlled laboratory study.
METHODS
Remnant articular cartilage was collected from fresh femoral condylar allografts. Cartilage samples were divided into 4 groups: cartilage explants with or without fibrin glue and mechanically minced cartilage with or without fibrin glue. Samples were cultured for 42 days. Chondrocyte viability was assessed using live/dead assay. Cellular migration and outgrowth were monitored using bright-field microscopy. Extracellular matrix deposition was assessed via histological staining. Proteoglycan content and synthesis were assessed using dimethylmethylene blue assay and radiolabeled 35S-sulfate, respectively. Type II collagen (COL2A1) gene expression was analyzed via polymerase chain reaction.
RESULTS
The mean viability of minced cartilage particles (34% ± 14%) was not significantly reduced compared with baseline (46% ± 13%) on day 0 (
CONCLUSION
Mechanically minced articular cartilage remained viable after 42 days of culture in vitro and was comparable with cartilage explants with regard to cellular migration, outgrowth, and extracellular matrix synthesis.
CLINICAL RELEVANCE
Mechanically minced articular cartilage is an encouraging intervention for the treatment of symptomatic cartilage defects. Further translational work is warranted to determine the viability of minced cartilage implantation as a single-stage therapeutic intervention in vivo.

Identifiants

pubmed: 35736385
doi: 10.1177/03635465221101004
doi:

Substances chimiques

Fibrin Tissue Adhesive 0
Proteoglycans 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2515-2525

Commentaires et corrections

Type : ErratumIn

Auteurs

Aghogho Evuarherhe (A)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Nolan B Condron (NB)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Derrick M Knapik (DM)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Eric D Haunschild (ED)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Ron Gilat (R)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Hailey P Huddleston (HP)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Joshua T Kaiser (JT)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Kevin C Parvaresh (KC)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Kyle R Wagner (KR)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Susan Chubinskaya (S)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Adam B Yanke (AB)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

Brian J Cole (BJ)

Midwest Orthopaedics at Rush University Medical Center, Chicago, Illinois, USA.

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Classifications MeSH