Abstract
There is a compelling need to develop novel therapies for diabetes mellitus. Recent successes in the transplantation of islets of Langerhans are seen as a major breakthrough. However, there is huge disparity between potential recipients and the availability of donor tissue. Human embryonic stem cells induced to form pancreatic beta cells could provide a replenishable supply of tissue. Early studies on the spontaneous differentiation of mouse embryonic stem cells have laid the foundation for a more directed approach based on recapitulating the events that occur during the development of the pancreas in the mouse. A high yield of definitive endoderm has been achieved, and although beta-like cells can be generated in a step-wise manner, the efficiency is still low and the final product is not fully differentiated. Future challenges include generating fully functional islet cells under Xeno-free and chemically defined conditions and circumventing the need for immunosuppression.
Original language | English |
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Pages (from-to) | 827-838 |
Number of pages | 12 |
Journal | Seminars in Cell & Developmental Biology |
Volume | 18 |
Issue number | 6 |
Early online date | 11 Sept 2007 |
DOIs | |
Publication status | Published - Dec 2007 |
Keywords
- differentiation
- Pdx1
- insulin gene
- regenerative medicine
- cell therapy
- pancreas development
- insulin-producing cells
- pancreatic beta-cells
- in-vitro
- islet transplantation
- definitive endoderm
- expressing cells
- nuclear transfer
- gene-expression
- ex-vivo
- directed differentiation