このエントリーをはてなブックマークに追加


ID 64148
フルテキストURL
fulltext.pdf 1.25 MB
著者
Fujisawa, Yuki Department of Regenerative Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Ming, Lu Department of Regenerative Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Yamada, Daisuke Department of Regenerative Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Takao, Tomoka Department of Regenerative Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Takarada, Takeshi Department of Regenerative Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
抄録
Tendon regeneration is difficult because detailed knowledge about tendon progenitor cells (TPCs), which produce tenocytes to repair tendon tissue, has not been revealed. Mohawk homeobox (MKX) is a marker of TPCs or tenocytes, but a human pluripotent stem cell (hPSC)-based reporter system that visualizes MKX+ cells has not been developed. Here, we established an hPSC-derived MKX-tdTomato reporter cell line and tested the induction ratio of MKX-tdTomato(+) cells using our stepwise/xeno-free differentiation protocol. MKX-tdTomato(+) cells were generated with high efficiency and expressed tendon-specific markers, including MKX, SCX, TNMD, and COL1A1. Our MKX-tdTomato hPSC line would be a useful tool for studying the development or regeneration of tendon tissue.
キーワード
Tendon
Human pluripotent stem cells
Tenocytes
Tendon regeneration
発行日
2022-11-12
出版物タイトル
STEM Cell Research & Therapy
13巻
1号
出版者
BMC
開始ページ
515
ISSN
1757-6512
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Author(s) 2022.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1186/s13287-022-03203-5
ライセンス
http://creativecommons.org/licenses/by/4.0/.
助成機関名
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development
助成番号
21H02643
18bm0704024h0001