Chan Brian Ho Ching, Moosajee Mariya, Rainger Joe
The Division of Functional Genetics and Development, The Royal Dick School of Veterinary Sciences, The Roslin Institute, The University of Edinburgh, Scotland, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.
Front Cell Dev Biol. 2021 Jan 11;8:620774. doi: 10.3389/fcell.2020.620774. eCollection 2020.
A key embryonic process that occurs early in ocular development is optic fissure closure (OFC). This fusion process closes the ventral optic fissure and completes the circumferential continuity of the 3-dimensional eye. It is defined by the coming together and fusion of opposing neuroepithelia along the entire proximal-distal axis of the ventral optic cup, involving future neural retina, retinal pigment epithelium (RPE), optic nerve, ciliary body, and iris. Once these have occurred, cells within the fused seam differentiate into components of the functioning visual system. Correct development and progression of OFC, and the continued integrity of the fused margin along this axis, are important for the overall structure of the eye. Failure of OFC results in ocular coloboma-a significant cause of childhood visual impairment that can be associated with several complex ocular phenotypes including microphthalmia and anterior segment dysgenesis. Despite a large number of genes identified, the exact pathways that definitively mediate fusion have not yet been found, reflecting both the biological complexity and genetic heterogeneity of the process. This review will highlight how recent developmental studies have become focused specifically on the epithelial fusion aspects of OFC, applying a range of model organisms (spanning fish, avian, and mammalian species) and utilizing emerging high-resolution live-imaging technologies, transgenic fluorescent models, and unbiased transcriptomic analyses of segmentally-dissected fissure tissue. Key aspects of the fusion process are discussed, including basement membrane dynamics, unique cell behaviors, and the identities and fates of the cells that mediate fusion. These will be set in the context of what is now known, and how these point the way to new avenues of research.
在眼部发育早期发生的一个关键胚胎过程是视裂闭合(OFC)。这个融合过程关闭了腹侧视裂,完成了三维眼球的圆周连续性。它是由沿着腹侧视杯的整个近端 - 远端轴相对的神经上皮细胞聚集和融合所定义的,涉及未来的神经视网膜、视网膜色素上皮(RPE)、视神经、睫状体和虹膜。一旦这些过程发生,融合缝内的细胞就会分化为功能性视觉系统的组成部分。OFC的正确发育和进展,以及沿着这个轴融合边缘的持续完整性,对眼睛的整体结构很重要。OFC失败会导致眼部缺损——这是儿童视力损害的一个重要原因,可能与几种复杂的眼部表型有关,包括小眼症和前段发育异常。尽管已经鉴定出大量基因,但尚未找到明确介导融合的确切途径,这反映了该过程的生物学复杂性和遗传异质性。本综述将重点介绍最近的发育研究如何特别关注OFC的上皮融合方面,应用一系列模式生物(包括鱼类、鸟类和哺乳动物物种),并利用新兴的高分辨率实时成像技术、转基因荧光模型以及对分段解剖的视裂组织进行无偏转录组分析。讨论了融合过程的关键方面,包括基底膜动态、独特的细胞行为以及介导融合的细胞的身份和命运。这些将在现有知识的背景下进行阐述,以及它们如何为新的研究途径指明方向。