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Directed neural differentiation of human embryonic stem cells via an obligated primitive anterior stage.

Author	Matthew T Pankratz, Xue-Jun Li, Timothy M Lavaute, Elizabeth A Lyons, Xin Chen, Su-Chun Zhang, Matthew T Pankratz, Xue-Jun Li, Timothy M Lavaute, Elizabeth A Lyons, Xin Chen, Su-Chun Zhang, Matthew T Pankratz, Xue-Jun Li, Timothy M Lavaute, Elizabeth A Lyons, Xin Chen, Su-Chun Zhang
Citation Information	Stem cells (Dayton, Ohio), 25:1511-20 (2007)
Keywords	Animals, Biological Markers, Cell Differentiation, Cells, Cultured, Ectoderm, Embryonic Stem Cells, Epithelial Cells, Gene Expression Profiling, Humans, Macaca mulatta, Models, Biological, Neurons, Time Factors
Related Products	AB9558
Pub Med ID	17332508

Understanding neuroectoderm formation and subsequent diversification to functional neural subtypes remains elusive. We show here that human embryonic stem cells (hESCs) differentiate to primitive neuroectoderm after 8-10 days. At this stage, cells uniformly exhibit columnar morphology and express neural markers, including anterior but not posterior homeodomain proteins. The anterior identity of these cells develops regardless of morphogens present during initial neuroectoderm specification. This anterior phenotype can be maintained or transformed to a caudal fate with specific morphogens over the next week, when cells become definitive neuroepithelia, marked by neural tube-like structures with distinct adhesion molecule expression, Sox1 expression, and a resistance to additional patterning signals. Thus, primitive neuroepithelia represents the earliest neural cells that possess the potential to differentiate to regionally specific neural progenitors. This finding offers insights into early human brain development and lays a foundation for generating neural cells with correct positional and transmitter profiles. Disclosure of potential conflicts of interest is found at the end of this article.