TY - JOUR
T1 - Transdifferentiation of human adipose tissue-derived stromal cells into insulin-producing clusters
AU - Okura, Hanayuki
AU - Komoda, Hiroshi
AU - Fumimoto, Yuichi
AU - Lee, Chun Man
AU - Nishida, Toshirou
AU - Sawa, Yoshiki
AU - Matsuyama, Akifumi
PY - 2009/6
Y1 - 2009/6
N2 - 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.
AB - 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.
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U2 - 10.1007/s10047-009-0455-6
DO - 10.1007/s10047-009-0455-6
M3 - Article
C2 - 19536630
AN - SCOPUS:67650699243
SN - 1434-7229
VL - 12
SP - 123
EP - 130
JO - Journal of Artificial Organs
JF - Journal of Artificial Organs
IS - 2
ER -