Effects of Micronized Cartilage Matrix on Cartilage Repair in Osteochondral Lesions of the Talus.


Journal

Cartilage
ISSN: 1947-6043
Titre abrégé: Cartilage
Pays: United States
ID NLM: 101518378

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 30 8 2018
medline: 17 8 2021
entrez: 30 8 2018
Statut: ppublish

Résumé

The repair of osteochondral lesions remains a challenge due to its poor vascularity and limited healing potential. Micronized cartilage matrix (MCM) is dehydrated, decellularized, micronized allogeneic cartilage matrix that contains the components of native articular tissue and is hypothesized to serve as a scaffold for the formation of hyaline-like tissue. Our objective was to demonstrate In group 1 (no wash), 250 µL MCM was reconstituted in 150 µL Dulbecco's phosphate-buffered saline (DPBS) for 5 minutes. Group 2 (saline wash) included 250 µL MCM washed in 20 mL DPBS for 30 minutes, then aspirated to remove all DPBS and reconstituted in 150 µL DPBS. Group 3 (serum wash): 250µL MCM washed in 20 mL DPBS for 30 minutes, then aspirated and reconstituted in 150 µL fetal bovine serum. Each group was then added to 50 µL solution of MSC suspended in DPBS at a concentration of 1.2 × 10 Stem cells without rehydration of the MCM showed almost no viability whereas near complete cell viability was seen after rehydration with serum or saline solution, ultimately leading to chondrogenic differentiation and adhesion to the MCM particles. We have shown in this proof-of-concept

Sections du résumé

BACKGROUND
The repair of osteochondral lesions remains a challenge due to its poor vascularity and limited healing potential. Micronized cartilage matrix (MCM) is dehydrated, decellularized, micronized allogeneic cartilage matrix that contains the components of native articular tissue and is hypothesized to serve as a scaffold for the formation of hyaline-like tissue. Our objective was to demonstrate
DESIGN
In group 1 (no wash), 250 µL MCM was reconstituted in 150 µL Dulbecco's phosphate-buffered saline (DPBS) for 5 minutes. Group 2 (saline wash) included 250 µL MCM washed in 20 mL DPBS for 30 minutes, then aspirated to remove all DPBS and reconstituted in 150 µL DPBS. Group 3 (serum wash): 250µL MCM washed in 20 mL DPBS for 30 minutes, then aspirated and reconstituted in 150 µL fetal bovine serum. Each group was then added to 50 µL solution of MSC suspended in DPBS at a concentration of 1.2 × 10
RESULTS
Stem cells without rehydration of the MCM showed almost no viability whereas near complete cell viability was seen after rehydration with serum or saline solution, ultimately leading to chondrogenic differentiation and adhesion to the MCM particles.
CONCLUSION
We have shown in this proof-of-concept

Identifiants

pubmed: 30156865
doi: 10.1177/1947603518796125
pmc: PMC7298590
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

316-322

Références

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Auteurs

Alvin K Shieh (AK)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

Sohni G Singh (SG)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

Connor Nathe (C)

University of California Irvine School of Medicine, Irvine, CA, USA.

Evan Lian (E)

Royal College of Surgeons in Ireland School of Medicine, Dublin, Ireland.

Dominik R Haudenschild (DR)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

Jan A Nolta (JA)

Institute for Regenerative Cures, University of California Davis Medical Center, Sacramento, CA, USA.

Cassandra A Lee (CA)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

Eric Giza (E)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

Christopher D Kreulen (CD)

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.

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Classifications MeSH