セキネ ヒデカズ   Sekine Hidekazu
  関根 秀一
   所属   医学研究科 医学研究科 (医学部医学科をご参照ください)
   職種   准教授
論文種別 原著
言語種別 日本語
査読の有無 査読あり
表題 Tricultured Cell Sheets Develop into Functional Pancreatic Islet Tissue with a Vascular Network.
掲載誌名 正式名:Tissue engineering. Part A
略  称:Tissue Eng Part A
ISSNコード:1937335X/19373341
掲載区分国外
巻・号・頁 29(7-8),211-224頁
著者・共著者 HOMMAJun†, SEKINEHidekazu*, SHIMIZUTatsuya
担当区分 2nd著者,責任著者
発行年月 2023/04
概要 Methods to induce islet β-cells from induced pluripotent stem cells or embryonic stem cells have been established. However, islet β-cells are susceptible to apoptosis under hypoxic conditions, so the technique used to transplant β-cells must maintain the viability of cells in vivo. This study describes the development of a tricultured cell sheet, which was made by coculturing islet β-cells, vascular endothelial cells, and mesenchymal stem cells for 1 day. The islet β-cells in the tricultured cell sheet self-organized into islet-like structures surrounded by a dense vascular network in vitro. Triple-layered tricultured cell sheets engrafted well after transplantation in vivo and developed into insulin-secreting tissue with abundant blood vessels and a high density of islet β-cells. We anticipate that the tricultured cell sheet could be used as an in vitro pseudo-islet model for pharmaceutical testing and may have potential for development into transplantable grafts for use in regenerative medicine. Impact statement This research assessed whether tricultured cell sheets containing islet β-cells, vascular endothelial cells, and mesenchymal stem cells were able to form islet tissue. There were two main findings. First, the islet β-cells in the tricultured cell sheet self-organized into islet structures surrounded by a dense vascular network in vitro. Second, triple-layered tricultured sheets engrafted well onto rat muscle and developed into insulin-secreting tissue with an abundance of blood vessels. The tricultured cell sheet could be used as a pseudo-islet model for pharmaceutical testing and may have potential for development into a transplantable graft for application in the clinical setting.
DOI 10.1089/ten.TEA.2022.0167
PMID 36565034