生物
胚胎干细胞
诱导多能干细胞
细胞生物学
干细胞
体外
科斯尔
细胞分化
胚状体
遗传学
基因
作者
Michio Noguchi,Kiminori Hosoda,Maiko Nakane,Eisaku Mori,Kazuhiro Nakao,Daisuke Taura,Yuji Yamamoto,Toru Kusakabe,Masakatsu Sone,Hidetoshi Sakurai,Junji Fujikura,Ken Ebihara,Kazuwa Nakao
出处
期刊:Stem Cells and Development
[Mary Ann Liebert, Inc.]
日期:2013-06-10
卷期号:22 (21): 2895-2905
被引量:30
标识
DOI:10.1089/scd.2013.0113
摘要
Human induced pluripotent stem (iPS) and embryonic stem (ES) cells can differentiate into a variety of cell types. We reported on adipogenic potential of human iPS and ES cells in vitro. In the present study, we investigate the survival and maintenance of adipocytes differentiated in vitro from human iPS and ES cells after transplantation. Following adipogenic induction in vitro, the differentiated cells exhibited functional properties of adipocytes such as lipid storage, lipolysis, and insulin responsiveness. Subsequently, Matrigel containing the differentiated human iPS and ES cells was transplanted into the subcutaneous tissue of nude mice. After 1-4 weeks, the cells with adipocyte-like features were observed in transplanted Matrigel by histological analysis. The human origin of the cells, their lipid accumulation, and gene expression of adipocyte markers in transplanted cells were then confirmed, suggesting the presence of adipocytes in transplanted Matrigel. When the relative areas of these cells were calculated by dividing the adipocyte areas by the total Matrigel areas, we found that they peaked at 2 weeks after transplantation, and that the adipocytes persisted at 4 weeks. The present study demonstrates that human iPS and ES cells can differentiate into adipocytes with functional properties and that adipocytes derived from human iPS and ES cells can survive and maintain the differentiated properties of adipocytes for at least 4 weeks after transplantation. Adipocytes derived from human iPS and ES cells thus have the potential to open new avenues for stem cell-based research into metabolic diseases and future therapeutic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI