Lee Hyun-Kyung, Lee Hyun-Shik, Moody Sally A
ABRC, School of Life Sciences, BK21 Plus KNU Creative BioReserach Group, Kyungpook National University, Daegu 702-702, Korea.
Mol Cells. 2014 Oct 31;37(10):705-12. doi: 10.14348/molcells.2014.0227. Epub 2014 Sep 18.
The early steps of neural development in the vertebrate embryo are regulated by sets of transcription factors that control the induction of proliferative, pluripotent neural precursors, the expansion of neural plate stem cells, and their transition to differentiating neural progenitors. These early events are critical for producing a pool of multipotent cells capable of giving rise to the multitude of neurons and glia that form the central nervous system. In this review we summarize findings from gain- and loss-of-function studies in embryos that detail the gene regulatory network responsible for these early events. We discuss whether this information is likely to be similar in mammalian embryonic and induced pluripotent stem cells that are cultured according to protocols designed to produce neurons. The similarities and differences between the embryo and stem cells may provide important guidance to stem cell protocols designed to create immature neural cells for therapeutic uses.
脊椎动物胚胎中神经发育的早期步骤受转录因子调控,这些转录因子控制增殖性多能神经前体的诱导、神经板干细胞的扩增以及它们向分化神经祖细胞的转变。这些早期事件对于产生一群多能细胞至关重要,这些多能细胞能够分化为构成中枢神经系统的众多神经元和神经胶质细胞。在本综述中,我们总结了胚胎功能获得和功能丧失研究的结果,这些研究详细阐述了负责这些早期事件的基因调控网络。我们讨论了在按照旨在生成神经元的方案培养的哺乳动物胚胎干细胞和诱导多能干细胞中,这些信息是否可能相似。胚胎与干细胞之间的异同可能为旨在创建用于治疗的未成熟神经细胞的干细胞方案提供重要指导。