Baye Lisa M, Link Brian A
Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Brain Res. 2008 Feb 4;1192:29-36. doi: 10.1016/j.brainres.2007.05.021. Epub 2007 May 23.
In this review we focus on the mechanisms, regulation, and cellular consequences of nuclear migration in the developing retina. In the nervous system, nuclear migration is prominent during both proliferative and post-mitotic phases of development. Interkinetic nuclear migration is the process where the nucleus oscillates from the apical to basal surfaces in proliferative neuroepithelia. Proliferative nuclear movement occurs in step with the cell cycle, with M-phase being confined to the apical surface and G1-, S-, and G2-phases occurring at more basal locations. Later, following cell cycle exit, some neuron precursors migrate by nuclear translocation. In this mode of cellular migration, nuclear movement is the driving force for motility. Following discussion of the key components and important regulators for each of these processes, we present an emerging model where interkinetic nuclear migration functions to distinguish cell fates among retinal neuroepithelia.
在本综述中,我们聚焦于发育中的视网膜中核迁移的机制、调控及其细胞后果。在神经系统中,核迁移在发育的增殖期和有丝分裂后期均十分显著。动核迁移是指在增殖性神经上皮中,细胞核从顶端表面向基底表面振荡的过程。增殖性核运动与细胞周期同步发生,M期局限于顶端表面,而G1期、S期和G2期则发生在更靠基底的位置。随后,在细胞周期退出后,一些神经元前体通过核转位进行迁移。在这种细胞迁移模式中,核运动是运动的驱动力。在讨论了这些过程各自的关键组成部分和重要调节因子后,我们提出了一个新出现的模型,即动核迁移在区分视网膜神经上皮细胞命运中发挥作用。