Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, Utah, USA.
Curr Top Dev Biol. 2010;93:61-84. doi: 10.1016/B978-0-12-385044-7.00003-5.
Organogenesis of the eye is a multistep process that starts with the formation of optic vesicles followed by invagination of the distal domain of the vesicles and the overlying lens placode resulting in morphogenesis of the optic cup. The late optic vesicle becomes patterned into distinct ocular tissues: the neural retina, retinal pigment epithelium (RPE), and optic stalk. Multiple congenital eye disorders, including anophthalmia or microphthalmia, aniridia, coloboma, and retinal dysplasia, stem from disruptions in embryonic eye development. Thus, it is critical to understand the mechanisms that lead to initial specification and differentiation of ocular tissues. An accumulating number of studies demonstrate that a complex interplay between inductive signals provided by tissue-tissue interactions and cell-intrinsic factors is critical to ensuring proper specification of ocular tissues as well as maintenance of RPE cell fate. While several of the extrinsic and intrinsic determinants have been identified, we are just at the beginning in understanding how these signals are integrated. In addition, we know very little about the actual output of these interactions. In this chapter, we provide an update of the mechanisms controlling the early steps of eye development in vertebrates, with emphasis on optic vesicle evagination, specification of neural retina and RPE at the optic vesicle stage, the process of invagination during morphogenesis of the optic cup, and maintenance of the RPE cell fate.
眼睛的发生是一个多步骤的过程,从视囊泡的形成开始,接着是囊泡远端的内陷和覆盖的晶状体基板,导致视神经杯的形态发生。晚期视囊泡被分化为不同的眼部组织:神经视网膜、视网膜色素上皮(RPE)和视神经柄。多种先天性眼部疾病,包括无眼或小眼、无虹膜、视网膜裂孔和视网膜发育不良,都源于胚胎眼部发育的中断。因此,了解导致眼部组织初始特化和分化的机制至关重要。越来越多的研究表明,组织间相互作用提供的诱导信号与细胞内在因素之间的复杂相互作用对于确保眼部组织的正确特化以及维持 RPE 细胞命运至关重要。虽然已经确定了一些外在和内在决定因素,但我们才刚刚开始理解这些信号是如何整合的。此外,我们对这些相互作用的实际结果知之甚少。在本章中,我们提供了对脊椎动物眼睛早期发育控制机制的最新更新,重点介绍了视囊泡的外凸、视神经泡阶段神经视网膜和 RPE 的特化、视神经杯形态发生过程中的内陷以及 RPE 细胞命运的维持。