Transdifferentiation of human adipose tissue-derived stromal cells into insulin-producing clusters

被引:64
|
作者
Okura, Hanayuki [2 ,3 ]
Komoda, Hiroshi [1 ]
Fumimoto, Yuichi [2 ]
Lee, Chun-Man [4 ]
Nishida, Toshirou [2 ]
Sawa, Yoshiki [2 ]
Matsuyama, Akifumi [1 ,4 ]
机构
[1] Fdn Biomed Res & Innovat, Lab Somat Stem Cell Therapy, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Osaka Univ, Grad Sch Med, Dept Surg, Osaka, Japan
[3] Japan Soc Promot Sci, Tokyo, Japan
[4] Osaka Univ Hosp, Med Ctr Translat Res, Osaka 553, Japan
关键词
Diabetes mellitus; Adipose tissue-derived stromal cells; Insulin; Islet-like cluster; Glucose response; EMBRYONIC STEM-CELLS; PANCREATIC ENDOCRINE; BONE-MARROW; ISLET TRANSPLANTATION; MULTIPOTENTIAL NESTIN; GROWTH-FACTORS; IN-VIVO; DIFFERENTIATION; PRECURSORS; PROGENITOR;
D O I
10.1007/s10047-009-0455-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Type 1 diabetes mellitus is caused by autoimmune destruction of insulin-producing beta cells. The major obstacle to transplantation of insulin-producing cells to cure the disease is the limited source of these cells. To overcome this problem, we describe here a multistep protocol for generation of insulin-producing islet-like clusters from human adipose tissue-derived stromal cells (ADSCs). Analysis using reverse transcription polymerase chain reaction detected enhanced expression of various pancreatic genes during the differentiation of ADSCs. Immunofluorescence analysis revealed functional similarities between cells derived from ADSCs and pancreatic islet cells, i.e., the presence of insulin- and C-peptide-coexpressing cells in the clusters and glucagon expression on the cell surface. The glucose challenge tests revealed the production of insulin, and such production was regulated via physiological signaling pathways. Our insulin-producing cells derived from ADSCs could be potentially used for cell therapy of type 1 diabetes mellitus.
引用
收藏
页码:123 / 130
页数:8
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