Arlotta Paola, Berninger Benedikt
Department of Stem Cell and Regenerative Biology, Harvard University, 7 Divinity Ave, Cambridge, USA.
Research group "Adult Neurogenesis and Cellular Reprogramming", Institute of Physiological Chemistry, and Focus Program Translational Neuroscience, University Medical Center, Johannes Gutenberg University Mainz, Hanns-Dieter-Hüsch-Weg 19, Mainz, Germany; Department of Physiological Genomics, Institute of Physiology, Ludwig Maximilians University Munich, Schillerstrasse 46, D-80336 Munich, Germany.
Curr Opin Neurobiol. 2014 Aug;27:208-14. doi: 10.1016/j.conb.2014.04.007. Epub 2014 May 4.
During embryonic development, uncommitted pluripotent cells undergo progressive epigenetic changes that lock them into a final differentiated state. Can mammalian cells change identity within the living organism? Direct lineage reprogramming of cells has attracted attention as a means to achieve organ regeneration. However, it is unclear whether cells in the CNS are endowed with the plasticity to reprogram. Neurons in particular are considered among the most immutable cell types, able to retain their class-specific traits for the lifespan of the organism. Here we focus on two experimental paradigms, glia-to-neuron and neuron-to-neuron conversion, to consider how lineage reprogramming has challenged the notion of CNS immutability, paving the way for the application of reprogramming strategies to reshape neurons and circuits in vivo.
在胚胎发育过程中,未分化的多能细胞会经历渐进性的表观遗传变化,从而使其锁定在最终的分化状态。哺乳动物细胞能否在活体生物体内改变其身份?细胞的直接谱系重编程作为实现器官再生的一种手段已引起关注。然而,目前尚不清楚中枢神经系统(CNS)中的细胞是否具有重编程的可塑性。特别是神经元被认为是最不易改变的细胞类型之一,能够在生物体的整个生命周期中保留其类别特异性特征。在这里,我们聚焦于两种实验范式,即胶质细胞向神经元的转化以及神经元向神经元的转化,以探讨谱系重编程如何挑战了中枢神经系统不可改变的观念,为应用重编程策略在体内重塑神经元和神经回路铺平了道路。