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Mesenchymal Stem Cell Extracellular Vesicles as Adjuvant to Bone Marrow Stimulation in Chondral Defect Repair in a Minipig Model.
Hede, Kris T C; Christensen, Bjørn B; Olesen, Morten L; Thomsen, Jesper Skovhus; Foldager, Casper B; Toh, Wei Seong; Lim, Sai Kiang; Lind, Martin C.
Afiliación
  • Hede KTC; Orthopedic Research Laboratory, Aarhus University Hospital, Aarhus N, Denmark.
  • Christensen BB; Orthopedic Research Laboratory, Aarhus University Hospital, Aarhus N, Denmark.
  • Olesen ML; Orthopedic Research Laboratory, Aarhus University Hospital, Aarhus N, Denmark.
  • Thomsen JS; Department of Biomedicine, Aarhus University, Aarhus C, Denmark.
  • Foldager CB; Orthopedic Research Laboratory, Aarhus University Hospital, Aarhus N, Denmark.
  • Toh WS; Faculty of Dentistry, National University of Singapore, Singapore.
  • Lim SK; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Lind MC; Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore.
Cartilage ; 13(2_suppl): 254S-266S, 2021 12.
Article en En | MEDLINE | ID: mdl-34308681
ABSTRACT

OBJECTIVE:

This study evaluated the effects of mesenchymal stem cell-extracellular vesicles (MSC-EVs) on chondrocyte proliferation in vitro and on cartilage repair in vivo following bone marrow stimulation (BMS) of focal chondral defects of the knee.

METHODS:

Six adult Göttingen minipigs received 2 chondral defects in each knee. The pigs were randomized to treatment with either BMS combined with MSC-EVs or BMS combined with phosphate-buffered saline (PBS). Intraarticular injections MSC-EVs or PBS were performed immediately after closure of the surgical incisions, and at 2 and 4 weeks postoperatively. Repair was evaluated after 6 months with gross examination, histology, histomorphometry, immunohistochemistry, and micro-computed tomography (µCT) analysis of the trabecular bone beneath the defect.

RESULTS:

Defects treated with MSC-EVs had more bone in the cartilage defect area than the PBS-treated defects (7.9% vs. 1.5%, P = 0.02). Less than 1% of the repair tissue in both groups was hyaline cartilage. International Cartilage and Joint Preservation Society II histological scoring showed that defects treated with MSC-EVs scored lower on "matrix staining" (20.8 vs. 50.0, P = 0.03), "cell morphology" (35.4 vs. 53.8, P = 0.04), and "overall assessment" (30.8 vs. 52.9, P = 0.03). Consistently, defects treated with MSC-EVs had lower collagen II and higher collagen I areal deposition. Defects treated with MSC-EVs had subchondral bone with significantly higher tissue mineral densities than PBS-treated defects (860 mg HA/cm3 vs. 838 mg HA/cm3, P = 0.02).

CONCLUSION:

Intraarticular injections of MSC-EVs in conjunction with BMS led to osseous ingrowth that impaired optimal cartilage repair, while enhancing subchondral bone healing.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cartílago Articular / Células Madre Mesenquimatosas / Vesículas Extracelulares Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Cartilage Año: 2021 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cartílago Articular / Células Madre Mesenquimatosas / Vesículas Extracelulares Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Cartilage Año: 2021 Tipo del documento: Article País de afiliación: Dinamarca