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Transplantation of Scaffold-Free Cartilage-Like Cell-Sheets Made from Human Bone Marrow Mesenchymal Stem Cells for Cartilage Repair: A Preclinical Study.
Itokazu, Maki; Wakitani, Shigeyuki; Mera, Hisashi; Tamamura, Yoshihiro; Sato, Yasushi; Takagi, Mutsumi; Nakamura, Hiroaki.
Afiliação
  • Itokazu M; Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan; School of Health and Sports Science, Mukogawa Women's University, Nishinomiya, Japan.
  • Wakitani S; School of Health and Sports Science, Mukogawa Women's University, Nishinomiya, Japan; Department of Artificial Joint & Biomaterials Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.
  • Mera H; School of Health and Sports Science, Mukogawa Women's University, Nishinomiya, Japan; International Medical Device Alliance, Foundation for Biomedical Research and Innovation, Kobe, Japan.
  • Tamamura Y; School of Health and Sports Science, Mukogawa Women's University, Nishinomiya, Japan.
  • Sato Y; Laboratory of Cell Processing Engineering, Division of Biotechnology and Macromolecular Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo, Japan.
  • Takagi M; Laboratory of Cell Processing Engineering, Division of Biotechnology and Macromolecular Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo, Japan.
  • Nakamura H; Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Cartilage ; 7(4): 361-72, 2016 Oct.
Article em En | MEDLINE | ID: mdl-27688844
ABSTRACT

OBJECTIVE:

The object of this study was to determine culture conditions that create stable scaffold-free cartilage-like cell-sheets from human bone marrow-derived mesenchymal stem cells (hBMSCs) and to assess their effects after transplantation into osteochondral defects in nude rats.

DESIGN:

(Experiment 1) The hBMSCs were harvested from 3 males, the proliferative and chondrogenic capacities were assessed at passage 1, and the cells were expanded in 3 different culture conditions (1) 5% fetal bovine serum (FBS), (2) 10% FBS, and (3) 5% FBS with fibroblast growth factor 2 (FGF-2). The cells were harvested and made chondrogenic pellet culture. The cell proliferation rate, glycosaminoglycan/DNA ratio, and safranin-O staining intensity of pellets cultured condition 3 were higher than those of conditions 1 and 2. (Experiment 2) The hBMSCs were expanded and passaged 3 times under culture condition 3, and fabricate the cell-sheets in chondrogenic medium either with or without FBS. The cell-sheets fabricated with FBS maintained their size with flat edges. (Experiment 3) The cell-sheets were transplanted into osteochondral defects in nude rats. Histological analysis was performed at 2, 4, and 12 weeks after surgery.

RESULTS:

The osteochondral repair was better after sheet transplantation than in the control group and significantly improved Wakitani score. Immunostaining with human-specific vimentin antibody showed that the transplanted cells became fewer and disappeared at 12 weeks.

CONCLUSIONS:

These results indicate that culture with FGF-2 may help to quickly generate sufficient numbers of cells to create stable and reliable scaffold-free cartilage-like cell-sheets, which contribute to the regeneration of osteochondral defects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cartilage Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cartilage Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão