論文

査読有り 国際誌
2020年4月

Gelatin Hydrogel-Fragmented Fibers Suppress Shrinkage of Cell Sheet.

Tissue engineering. Part C, Methods
  • Koichiro Nakamura
  • ,
  • Kimiaki Nobutani
  • ,
  • Naoki Shimada
  • ,
  • Yasuhiko Tabata

26
4
開始ページ
216
終了ページ
224
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1089/ten.tec.2019.0348

The objective of this study is to investigate the utility of gelatin hydrogel-fragmented fibers (GHFF) as a material to suppress the shrinkage of cell sheets, which often happens upon detaching from a culture plate. The GHFF were fabricated by cutting gelatin hydrogel nonwoven fabrics. MC3T3-E1 cells were simply mixed with different amounts of GHFF, followed by culturing to formulate the cell sheet homogeneously incorporating GHFF. When detached from the culture plate, the cell sheet formulated without GHFF shrunk while the area became about 23% of the original one before detachment. On the contrary, the cell sheet formulated with GHFF hardly shrunk. The lactate/glucose ratio of a metabolic activity was significantly lower and the adenosine triphosphate (ATP) production was higher for the cell sheet formulated with the GHFF than that obtained without the GHFF. An osteogenic activity was high for the cell sheet formulated with the GHFF compared with that obtained without the GHFF. The GHFF addition was a simple and promising method to fabricate active cell sheets without size change. Impact Statement This study introduces the utility of gelatin hydrogel-fragmented fibers (GHFF) for cell sheet engineering. Upon detaching from the culture plate, the cell sheet formulated without GHFF shrunk, while the area became about 23% of the original one before detachment. On the contrary, the cell sheet formulated with GHFF hardly shrunk. The GHFF allowed cell sheets to enhance the metabolic and osteogenic activities. The GHFF addition was a simple and promising method to fabricate active cell sheets without size change.

リンク情報
DOI
https://doi.org/10.1089/ten.tec.2019.0348
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32202972
ID情報
  • DOI : 10.1089/ten.tec.2019.0348
  • PubMed ID : 32202972

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