The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Activin A Efficiently Specifies Definitive Endoderm from Human Embryonic Stem Cells Only When Phosphatidylinositol 3-Kinase Signaling Is Suppressed
Open accessAbstract
Human ESCs (hESCs) respond to signals that determine their pluripotency, proliferation, survival, and differentiation status. In this report, we demonstrate that phosphatidylinositol 3-kinase (PI3K) antagonizes the ability of hESCs to differentiate in response to transforming growth factor β family members such as Activin A and Nodal. Inhibition of PI3K signaling efficiently promotes differentiation of hESCs into mesendoderm and then definitive endoderm (DE) by allowing them to be specified by Activin/Nodal signals present in hESC cultures. Under conditions where hESCs are grown in mouse embryo fibroblast-conditioned medium under feeder-free conditions, ∼70%–80% are converted into DE following 5 days of treatment with inhibitors of the PI3K pathway, such as LY 294002 and AKT1-II. Microarray and quantitative polymerase chain reaction-based gene expression profiling demonstrates that definitive endoderm formation under these conditions closely parallels that following specification with elevated Activin A and low fetal calf serum (FCS)/knockout serum replacement (KSR). Reduced insulin/insulin-like growth factor (IGF) signaling was found to be critical for cell fate commitment into DE. Levels of insulin/IGF present in FCS/KSR, normally used to promote self-renewal of hESCs, antagonized differentiation. In summary, we show that generation of hESC-DE requires two conditions: signaling by Activin/Nodal family members and release from inhibitory signals generated by PI3K through insulin/IGF. These findings have important implications for our understanding of hESC self-renewal and early cell fate decisions.
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Cites
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Production of pancreatic hormone–expressing endocrine cells from human embryonic stem cells
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Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells
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Self-citationA small molecule that directs differentiation of human ESCs into the pancreatic lineage
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Metadata
- Authors
- McLean, A. B., D'Amour, K. A., Jones, K. L., Krishnamoorthy, M., Kulik, M. J., Reynolds, D. M., Sheppard, A. M., Liu, H., Xu, Y., Baetge, E. E., & Dalton, S.
- Venue
- Stem Cells
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-01-01
- Volume
- 25
- Issue
- 1
- Pages
- 29-38
- ISSN
- 1066-5099 (ISSN-L)
- 1549-4918
- OpenAlex
- W2095298909
- Cited by
- 472
- References
- 28
- FWCI
- 12.57
- Type
- journal article
- Language
- en
- Open access
- bronze
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