Source:http://linkedlifedata.com/resource/pubmed/id/19255591
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2009-4-2
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pubmed:abstractText |
Human pluripotent stem cells represent a potentially unlimited source of functional pancreatic endocrine lineage cells. Here we report a highly efficient approach to induce human embryonic stem (ES) cells and induced pluripotent stem (iPS) cells to differentiate into mature insulin-producing cells in a chemical-defined culture system. The differentiated human ES cells obtained by this approach comprised nearly 25% insulin-positive cells as assayed by flow cytometry analysis, which released insulin/C-peptide in response to glucose stimuli in a manner comparable to that of adult human islets. Most of these insulin-producing cells co-expressed mature beta cell-specific markers such as NKX6-1 and PDX1, indicating a similar gene expression pattern to adult islet beta cells in vivo. In this study, we also demonstrated that EGF facilitates the expansion of PDX1-positive pancreatic progenitors. Moreover, our protocol also succeeded in efficiently inducing human iPS cells to differentiate into insulin-producing cells. Therefore, this work not only provides a new model to study the mechanism of human pancreatic specialization and maturation in vitro, but also enhances the possibility of utilizing patient-specific iPS cells for the treatment of diabetes.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/C-Peptide,
http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/NKX6-1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/pancreatic and duodenal homeobox 1...
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1748-7838
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
429-38
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pubmed:dateRevised |
2011-6-1
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pubmed:meshHeading |
pubmed-meshheading:19255591-C-Peptide,
pubmed-meshheading:19255591-Cell Differentiation,
pubmed-meshheading:19255591-Cells, Cultured,
pubmed-meshheading:19255591-Embryonic Stem Cells,
pubmed-meshheading:19255591-Epidermal Growth Factor,
pubmed-meshheading:19255591-Flow Cytometry,
pubmed-meshheading:19255591-Homeodomain Proteins,
pubmed-meshheading:19255591-Humans,
pubmed-meshheading:19255591-Insulin-Secreting Cells,
pubmed-meshheading:19255591-Pluripotent Stem Cells,
pubmed-meshheading:19255591-Trans-Activators
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pubmed:year |
2009
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pubmed:articleTitle |
Highly efficient differentiation of human ES cells and iPS cells into mature pancreatic insulin-producing cells.
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pubmed:affiliation |
Key Laboratory of Cell Proliferation and Differentiation of the Ministry of Education, College of Life Sciences, Peking University, Beijing 100871, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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