Department of Anatomy, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Department of Anatomy and Neuroscience, University College Cork, Cork, Ireland.
J Anat. 2019 Feb;234(2):216-226. doi: 10.1111/joa.12907. Epub 2018 Nov 25.
Glycosylation is a major post-translational modification in which a carbohydrate known as a glycan is enzymatically attached to target proteins which regulate protein folding and stability. Glycans are strongly expressed in the developing nervous system where they play multiple roles during development. The importance of these glycan epitopes in neural development is highlighted by a group of conditions known as congenital disorders of glycosylation which lead to psychomotor difficulties, mental retardation, lissencephaly, microencephaly and epilepsy. One of these glycan epitopes, known as Lewis X, is recognised by the FORSE-1 antibody and is regionally expressed in the developing nervous system. In this study, we report the regional and temporal expression patterns of FORSE-1 immunolabelling during the periods of neurogenesis, gliogenesis and axonogenesis in developing mouse nervous system. We demonstrate the localisation of FORSE-1 on subsets of neuroepithelial cells and radial glial cells, and in compartments corresponding to axon tract formation. These spatial, temporal and regional expression patterns are suggestive of roles in the determination of different cell lineages and in the patterning of white matter during development, and help provide insights into the neuroanatomical regions affected by congenital disorders of glycosylation.
糖基化是一种主要的翻译后修饰,其中一种称为聚糖的碳水化合物通过酶被连接到靶蛋白上,这些靶蛋白调节蛋白质的折叠和稳定性。聚糖在发育中的神经系统中强烈表达,在那里它们在发育过程中发挥多种作用。一组称为先天性糖基化紊乱的疾病突出了这些糖基化表位在神经发育中的重要性,这些疾病导致精神运动困难、智力迟钝、无脑回、小头畸形和癫痫。这些糖基化表位之一,称为 Lewis X,被 FORSE-1 抗体识别,并在发育中的神经系统中具有区域性表达。在这项研究中,我们报告了 FORSE-1 免疫标记在神经发生、神经胶质发生和轴突发生期间在发育中的小鼠神经系统中的区域和时间表达模式。我们证明了 FORSE-1 在神经上皮细胞和放射状胶质细胞的亚群上的定位,以及在对应于轴突束形成的隔室中的定位。这些空间、时间和区域表达模式表明其在决定不同细胞谱系和发育过程中白质模式方面的作用,并有助于深入了解先天性糖基化紊乱影响的神经解剖区域。