Zinin Nikolay, Adameyko Igor, Wilhelm Margareta, Fritz Nicolas, Uhlén Per, Ernfors Patrik, Henriksson Marie Arsenian
Department of Microbiology, Tumor and Cell Biology (MTC) Karolinska Institutet, Stockholm, Sweden.
EMBO Rep. 2014 Apr;15(4):383-91. doi: 10.1002/embr.201337424. Epub 2014 Mar 5.
The role of MYC proteins in somatic stem and progenitor cells during development is poorly understood. We have taken advantage of a chick in vivo model to examine their role in progenitor cells of the developing neural tube. Our results show that depletion of endogenous MYC in radial glial precursors (RGPs) is incompatible with differentiation and conversely, that overexpression of MYC induces neurogenesis independently of premature or upregulated expression of proneural gene programs. Unexpectedly, the neurogenic function of MYC depends on the integrity of the polarized neural tissue, in contrast to the situation in dissociated RGPs where MYC is mitogenic. Within the polarized RGPs of the neural tube, MYC drives differentiation by inhibiting Notch signaling and by increasing neurogenic cell division, eventually resulting in a depletion of progenitor cells. These results reveal an unexpected role of MYC in the control of stemness versus differentiation of neural stem cells in vivo.
MYC蛋白在发育过程中对体细胞干细胞和祖细胞的作用目前了解甚少。我们利用鸡体内模型来研究它们在发育中的神经管祖细胞中的作用。我们的结果表明,放射状胶质前体细胞(RGPs)中内源性MYC的缺失与分化不相容,相反,MYC的过表达可独立于神经源性基因程序的过早或上调表达而诱导神经发生。出乎意料的是,与解离的RGPs中MYC具有促有丝分裂作用的情况相反,MYC的神经发生功能取决于极化神经组织的完整性。在神经管的极化RGPs中,MYC通过抑制Notch信号传导和增加神经源性细胞分裂来驱动分化,最终导致祖细胞耗竭。这些结果揭示了MYC在体内控制神经干细胞干性与分化方面的意外作用。