Abstract
Surrogate β-cells derived from available adult stem cells are urgently needed for the treatment of insulindeficient diabetes, and hepatocytes constitute an attractive alternative. Herein, we attempted to generate insulin-producing cells from adult mouse primary hepatocytes (HCs) using triple adenoviruses harboring PDX-1/VP-16, BETA2, and MafA. We noted characteristic changes in the transduced HCs into pancreatic β-cells, including reduced albumin gene and increased insulin, insulin content, and the expression of a variety of pancreatic genes. Glucose tolerance and survival are improved by the renal capsular transplantation. These data demonstrated that the transdifferentiation of HCs into insulin-producing cells could be achieved under both in vitro and in vivo conditions. Further, these data suggest that induction of insulin-producing cells from liver provides a potential cell-replacement therapy for the treatment of patients with diabetes using alternative transplantable cell source.
| Original language | English |
|---|---|
| Pages (from-to) | 564-573 |
| Number of pages | 10 |
| Journal | Tissue Engineering and Regenerative Medicine |
| Volume | 8 |
| Issue number | 6 |
| State | Published - Nov 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- BETA2
- Hepatocyte
- MafA
- PDX-1
- Pancreatic β-cells
- Transdifferentiation
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