Mathieu Julie, Ruohola-Baker Hannele
Department of Biochemistry, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA.
Department of Biochemistry, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA
Development. 2017 Feb 15;144(4):541-551. doi: 10.1242/dev.128389.
Pluripotent cells from the early stages of embryonic development have the unlimited capacity to self-renew and undergo differentiation into all of the cell types of the adult organism. These properties are regulated by tightly controlled networks of gene expression, which in turn are governed by the availability of transcription factors and their interaction with the underlying epigenetic landscape. Recent data suggest that, perhaps unexpectedly, some key epigenetic marks, and thereby gene expression, are regulated by the levels of specific metabolites. Hence, cellular metabolism plays a vital role beyond simply the production of energy, and may be involved in the regulation of cell fate. In this Review, we discuss the metabolic changes that occur during the transitions between different pluripotent states both and , including during reprogramming to pluripotency and the onset of differentiation, and we discuss the extent to which distinct metabolites might regulate these transitions.
胚胎发育早期的多能细胞具有无限自我更新能力,并能分化为成体生物的所有细胞类型。这些特性受严格控制的基因表达网络调控,而该网络又受转录因子的可用性及其与潜在表观遗传格局的相互作用支配。最近的数据表明,或许出人意料的是,一些关键的表观遗传标记以及基因表达受特定代谢物水平的调控。因此,细胞代谢的作用不仅限于简单的能量产生,还可能参与细胞命运的调控。在本综述中,我们讨论了不同多能状态之间转换过程中发生的代谢变化,包括重编程为多能性以及分化开始阶段的代谢变化,并探讨了不同代谢物对这些转换的调控程度。