PDX-1 induces differentiation of intestinal epithelioid IEC-6 into insulin-producing cells

被引:95
作者
Yoshida, S
Kajimoto, Y
Yasuda, T
Watada, H
Fujitani, Y
Kosaka, H
Gotow, T
Miyatsuka, T
Umayahara, Y
Yamasaki, Y
Hori, M
机构
[1] Osaka Univ, Grad Sch Med, Dept Internal Med & Therapeut, Suita, Osaka 5650871, Japan
[2] Kohshien Univ, Coll Nutr, Takarazuka, Hyogo, Japan
[3] Osaka Univ, Grad Sch Med, Dept Dermatol, Suita, Osaka, Japan
关键词
D O I
10.2337/diabetes.51.8.2505
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A homeodomain containing transcription factor PDX-1 can induce beta-cell-specific gene expressions in some non beta-cells and may therefore. be useful for future diabetes gene/cell therapy. Among the potential target organs or tissues for transcription factor-mediated induction of beta-cell-like differentiation are the intestinal epithelial cells. They have, certain. merits over other tissues and organs in terms of accessibility for gene delivery and of similarity in developmental background to the pancreatic primordium. In this study, we used an intestinal epithelium-derived cell line, IEC-6 cells, And investigated. the possible effects of PDX-1 expression in those cells. By exogenous expression of the PDX-1 gene, IEC-6 cells started expressing multiple beta-cell-specific genes such, as amylin, glucokinase, and Nkx6.1 which were not found in the original IEC-6 cells. Insulin genie expression, which was missing, initially even in the PDX-1-transfected IEC-6 cells, became detectable when the cells were transplanted under the renal capsule of a rat. When the, PDX-1(+) IEC-6 cells were kept in vitro, treatment with betacellulin could also confer insulin gene, expression to them. Although insulin secretory granules became visible by election microscopy, they were secreted regardless of glucose concentration. The in vivo or in vitro inductions of the insulin gene expression were not observed in the PDX-1(-) IEC-6 cells.. Thus, our present observations demonstrate the potency of intestinal epithelial cells As a tool for diabetes gene/cell therapy 440 provide further support. for the potency of PDX-1 in driving beta-cell-like differentiation in non-beta-cells.
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页码:2505 / 2513
页数:9
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