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Effects of Micronized Cartilage Matrix on Cartilage Repair in Osteochondral Lesions of the Talus.
Shieh, Alvin K; Singh, Sohni G; Nathe, Connor; Lian, Evan; Haudenschild, Dominik R; Nolta, Jan A; Lee, Cassandra A; Giza, Eric; Kreulen, Christopher D.
Afiliación
  • Shieh AK; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
  • Singh SG; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
  • Nathe C; University of California Irvine School of Medicine, Irvine, CA, USA.
  • Lian E; Royal College of Surgeons in Ireland School of Medicine, Dublin, Ireland.
  • Haudenschild DR; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
  • Nolta JA; Institute for Regenerative Cures, University of California Davis Medical Center, Sacramento, CA, USA.
  • Lee CA; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
  • Giza E; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
  • Kreulen CD; Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, CA, USA.
Cartilage ; 11(3): 316-322, 2020 07.
Article en En | MEDLINE | ID: mdl-30156865
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 in vitro that the use of MCM combined with mesenchymal stem cells (MSCs) can lead to the formation of hyaline-like cartilage tissue in a single-stage treatment model. 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 × 106 cells/350 µL. After 3 weeks, the defects were extracted and sectioned to perform viability and histologic analyses. 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 in vitro study that MCM can serve as a scaffold for the growth of cartilage tissue for the treatment of osteochondral lesions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Astrágalo / Ingeniería de Tejidos / Cartílago Hialino / Matriz Extracelular / Andamios del Tejido Límite: Humans Idioma: En Revista: Cartilage Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Astrágalo / Ingeniería de Tejidos / Cartílago Hialino / Matriz Extracelular / Andamios del Tejido Límite: Humans Idioma: En Revista: Cartilage Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos