| Literature DB >> 21607105 |
Abstract
The success achieved over the last decade with islet transplantation has intensified interest in treating diabetes, not only by cell transplantation, but also by stem cells. The formation of insulin-producing cells from pancreatic duct, acinar, and liver cells is an active area of investigation. Protocols for the in vitro differentiation of embryonic stem (ES) cells based on normal developmental processes, have generated insulin-producing cells, though at low efficiency and without full responsiveness to extracellular levels of glucose. Induced pluripotent stem cells, which have been generated from somatic cells by introducing Oct3/4, Sox2, Klf4, and c-Myc, and which are similar to ES cells in morphology, gene expression, epigenetic status and differentiation, can also differentiate into insulin-producing cells. Overexpression of embryonic transcription factors in stem cells could efficiently induce their differentiation into insulin-expressing cells. The purpose of this review is to demonstrate recent progress in the research for new sources of β-cells, and to discuss strategies for the treatment of diabetes.Entities:
Keywords: Embryonic stem cells; Islet transplantation; Islets; Pancreatic stem cells; Pancreatic β-cells
Year: 2009 PMID: 21607105 PMCID: PMC3097914 DOI: 10.4252/wjsc.v1.i1.36
Source DB: PubMed Journal: World J Stem Cells ISSN: 1948-0210 Impact factor: 5.326