Raymond S M, Jackson I J
MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
Curr Biol. 1995 Nov 1;5(11):1286-95. doi: 10.1016/s0960-9822(95)00255-7.
During development of the vertebrate eye, there is a series of reciprocal cellular interactions that determine the fate of the eye components. Although evidence from organ culture suggests that the retinal pigmented epithelium (RPE) organizes the laminar structure of the differentiated neural retina, no role has been identified for the RPE in early eye development, nor has the later function of RPE been demonstrated in vivo.
To investigate the role of RPE cells in eye development, we generated transgenic mice that carry the attenuated diphtheria toxin-A gene; this transgene was driven by the promoter of the gene encoding the tyrosinase-related protein-1, which is specifically expressed in pigment cells. Depending on the expression level of the transgene, the retinal epithelium was ablated before or after its differentiation into a pigmented cell layer. We show that an early ablation (embryonic day E10-11) resulted in disorganization of the retinal layer, immediate arrest of eye growth and subsequent eye resorption. A later ablation (E11.5-12.5) allowed the eye to be maintained during embryogenesis, but the laminar structure of the retina became disrupted by the end of gestation, the vitreous failed to accumulate the adults were anophthalmic or severely microphthalmic. In some microphthalmic eyes, a number of RPE cells escaped ablation and formed patches of pigmented cells; the laminar structure of the retina was maintained immediately adjacent to such pigmented areas but disrupted elsewhere. In both cases--early or late ablation of the RPE--the retina appears to be the primary affected tissue.
We conclude that presence of the RPE is required for the normal development of the eye in vivo. Its presence early in development is necessary for the correct morphogenesis of the neural retina. After the neural retina has started to differentiate, the RPE is still necessary, either directly or indirectly, to maintain the organization of the retinal lamina.
在脊椎动物眼睛发育过程中,存在一系列相互作用的细胞活动,这些活动决定了眼睛各组成部分的命运。虽然器官培养的证据表明视网膜色素上皮(RPE)组织了分化的神经视网膜的层状结构,但尚未确定RPE在眼睛早期发育中的作用,也未在体内证明RPE的后期功能。
为了研究RPE细胞在眼睛发育中的作用,我们构建了携带减毒白喉毒素A基因的转基因小鼠;该转基因由编码酪氨酸酶相关蛋白-1的基因启动子驱动,该蛋白在色素细胞中特异性表达。根据转基因的表达水平,视网膜上皮在分化为色素细胞层之前或之后被消融。我们发现早期消融(胚胎第10 - 11天)导致视网膜层结构紊乱,眼睛生长立即停止并随后发生眼球吸收。后期消融(胚胎第11.5 - 12.5天)使眼睛在胚胎发育期间得以维持,但在妊娠末期视网膜的层状结构被破坏,玻璃体未能积聚,成年小鼠无眼或严重小眼。在一些小眼的眼睛中,一些RPE细胞逃脱了消融并形成了色素细胞斑块;视网膜的层状结构在紧邻这些色素区域处得以维持,但在其他地方被破坏。在这两种情况下——RPE的早期或晚期消融——视网膜似乎是主要受影响的组织。
我们得出结论,RPE的存在是眼睛在体内正常发育所必需的。其在发育早期的存在对于神经视网膜的正确形态发生是必要的。在神经视网膜开始分化后,RPE仍然是维持视网膜层组织所必需的,无论是直接还是间接。