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KMID : 1199120090330060475
Korean Diabetes Journal
2009 Volume.33 No. 6 p.475 ~ p.484
Transdifferentiation of Enteroendocrine K-cells into Insulin-expressing Cells
Lee Esder

Ko Seung-Hyun
Ahn Yu-Bae
Song Ki-Ho
Lee Min-Kyung
Ryu Ryul-Gyeong
Moon Sung-Dae
Yu Jun-Mo
Abstract
Background: Despite a recent breakthough in human islet transplantation for treating type 1 diabetes mellitus, the limited availability of donor pancreases remains a major obstacle. Endocrine cells within the gut epithelium (enteroendocrine cells) and pancreatic ¥â cells share similar pathways of differentiation during embryonic development. In particular, K-cells that secrete glucose-dependent insulinotropic polypeptide (GIP) have been shown to express many of the key proteins found in ¥â cells. Therefore, we hypothesize that K-cells can be transdifferentiated into ¥â cells because both cells have remarkable similarities in their embryonic development and cellular phenotypes.

Methods: K-cells were purified from heterogeneous STC-1 cells originating from an endocrine tumor of a mouse intestine. In addition, a K-cell subclone expressing stable Nkx6.1, called "Kn4-cells," was successfully obtained. In vitro differentiation of K-cells or Kn4-cells into ¥â cells was completed after exendin-4 treatment and serum deprivation. The expressions of insulin mRNA and protein were examined by RT-PCR and immunocytochemistry. The interacellular insulin content was also measured.

Results: K-cells were found to express glucokinase and GIP as assessed by RT-PCR and Western blot analysis. RT-PCR showed that K-cells also expressed Pdx-1, NeuroD1/Beta2, and MafA, but not Nkx6.1. After exendin-4 treatment and serum deprivation, insulin mRNA and insulin or C-peptide were clearly detected in Kn4-cells. The intracellular insulin content was also increased significantly in these cells.

Conclusion: K-cells are an attractive potential source of insulin-producing cells for treatment of type 1 diabetes mellitus. However, more experiments are necessary to optimize a strategy for converting K-cells into ¥â cells.
KEYWORD
Differentiation, Enteroendocrine cells, K-cell, Nkx6.1 protein, Pancreatic beta-cell
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