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MBP-FGF2-Immobilized Matrix Maintains Self-Renewal and Myogenic Differentiation Potential of Skeletal Muscle Stem Cells.
Sah, Jay Prakash; Hao, Nguyen Thi Thu; Kim, Yunhye; Eigler, Tamar; Tzahor, Eldad; Kim, Sang-Heon; Hwang, Yongsung; Yoon, Jeong Kyo.
Afiliação
  • Sah JP; Soonchunhyang Institute of Medi-bio Science, Soon Chun Hyang University, Cheonan, Korea.
  • Hao NTT; Department of Integrated Biomedical Science, Graduate School, Soon Chun Hyang University, Asan, Korea.
  • Kim Y; Soonchunhyang Institute of Medi-bio Science, Soon Chun Hyang University, Cheonan, Korea.
  • Eigler T; Department of Integrated Biomedical Science, Graduate School, Soon Chun Hyang University, Asan, Korea.
  • Tzahor E; Soonchunhyang Institute of Medi-bio Science, Soon Chun Hyang University, Cheonan, Korea.
  • Kim SH; Department of Integrated Biomedical Science, Graduate School, Soon Chun Hyang University, Asan, Korea.
  • Hwang Y; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
  • Yoon JK; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Int J Stem Cells ; 12(2): 360-366, 2019 Jul 30.
Article em En | MEDLINE | ID: mdl-30836735
ABSTRACT
The robust capacity of skeletal muscle stem cells (SkMSCs, or satellite cells) to regenerate into new muscles in vivo has offered promising therapeutic options for the treatment of degenerative muscle diseases. However, the practical use of SkMSCs to treat muscle diseases is limited, owing to their inability to expand in vitro under defined cultivation conditions without loss of engraftment efficiency. To develop an optimal cultivation condition for SkMSCs, we investigated the behavior of SkMSCs on synthetic maltose-binding protein (MBP)-fibroblast growth factor 2 (FGF2)-immobilized matrix in vitro. We found that the chemically well-defined, xeno-free MBP-FGF2-immobilized matrix effectively supports SkMSC growth without reducing their differentiation potential in vitro. Our data highlights the possible application of the MBP-FGF2 matrix for SkMSC expansion in vitro.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Stem Cells Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Stem Cells Ano de publicação: 2019 Tipo de documento: Article