## Abstract Availability of human embryonic stem cells (hESC) has enhanced human neural differentiation research. The derivation of neural progenitor (NP) cells from hESC facilitates the interrogation of human embryonic development through the generation of neuronal subtypes and supporting glial ce
Generation of neural crest progenitors from human embryonic stem cells
β Scribed by Nyam-Osor Chimge; Dashzeveg Bayarsaihan
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 227 KB
- Volume
- 314B
- Category
- Article
- ISSN
- 1552-5007
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The neural crest (NC) is a transient population of multipotent progenitors arising at the lateral edge of the neural plate in vertebrate embryos, which then migrate throughout the body to generate diverse array of tissues such as the peripheral nervous system, skin melanocytes, and craniofacial cartilage, bone and teeth. The transient nature of neural crest stem cells make extremely challenging to study the biology of these important cells. In humans induction and differentiation of embryonic NC occurs very early, within a few weeks of fertilization giving rise to technical and ethical issues surrounding isolation of early embryonic tissues and therefore severely limiting the study of human NC cells. For that reason our current knowledge of the biology of NC mostly derives from the studies of lower organisms. Recent progress in human embryonic stem cell research provides a unique opportunity for generation of a useful source of cells for basic developmental studies. The development of costβeffective, time and labor efficient improved differentiation protocols for the production of human NC cells is a critical step toward a better understanding of NC biology. J. Exp. Zool. (Mol. Dev. Evol.) 314B:95β103, 2010. Β© 2009 WileyβLiss, Inc.
π SIMILAR VOLUMES
## Abstract Embryonic stem cell (ESC)βderived products have emerged as a promising cell source for neuroregeneration. C17.2 neural precursor cells were noted to express genes of neurotrophins and neuroprotective factors and to be enable to enhance proliferation, neuritogenesis, and differentiation
The team of Liu et al. generated endoderm-derived human induced pluripotent stem (iPS) cells from primary hepatocytes. 1 However, they generated human iPS cells by using viral transgenes. 1 Clinical applications of human iPS cells require avoiding viral transgenes. On the other hand, the reprogrammi
## Abstract Temporal analysis in gene expression during differentiation of neural stem cells (NSCs) was performed by using inβhouse microarrays composed of 10,368 genes. The changes in mRNA level were measured during differentiation day 1, 2, 3, 6, 12, and 15. Out of 10,368 genes analyzed, 259 gene
## Abstract A reliable method to induce neural progenitor/stem cells (NPCs) into dopaminergic (DAergic) neurons has not yet been established. As well, the mechanism involved remains to be elucidated. To induce DAergic differentiation from NPCs, a cytokine mixture (CβMix) of interleukin (IL)β1Ξ², ILβ