Skeletal muscle‐adipose cocultured tissue fabricated using cell‐laden microfibers and a hydrogel sheet
The emerging interest in skeletal muscle tissue originates from its unique properties that control body movements. In particular, recent research advances in engineered skeletal muscle tissue have broadened the possibilities of applications in nonclinical models. However, due to the lack of adipose...
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Veröffentlicht in: | Biotechnology and bioengineering 2022-02, Vol.119 (2), p.636-643 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The emerging interest in skeletal muscle tissue originates from its unique properties that control body movements. In particular, recent research advances in engineered skeletal muscle tissue have broadened the possibilities of applications in nonclinical models. However, due to the lack of adipose tissue, current engineered skeletal muscle tissue has the limitation of satisfying in vivo‐like position and proportion of intermuscular fat. Adipose tissue within the skeletal muscle affects their functional properties. Here, a fabrication method for cocultured tissue composed of skeletal muscle and adipose tissues is proposed to reproduce the functional and morphological characteristics of muscle. By implementing prematured adipose microfibers in a myoblast‐laden hydrogel sheet, both the accumulation of large lipid droplets and control of the position of adipose tissue within the skeletal muscle tissue becomes feasible. The findings of this study provide helpful information regarding engineered skeletal muscle, which has strong potential in drug screening models.
This study describes a fabrication method for cocultured tissue composed of skeletal muscle and adipose tissues to reproduce the functional and morphological characteristics of muscle. Prematured adipose microfibers were implemented in a myoblast‐laden hydrogel sheet and cocultured for further maturation. The proposed method has potentials for the emerging field of in vitro tissue models for drug screening models. |
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ISSN: | 0006-3592 1097-0290 |
DOI: | 10.1002/bit.27989 |