Schmitt E A, Dowling J E
Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
J Comp Neurol. 1996 Jul 22;371(2):222-34. doi: 10.1002/(SICI)1096-9861(19960722)371:2<222::AID-CNE3>3.0.CO;2-4.
Earlier studies suggested retinal differentiation in the zebrafish commences ventrally rather than centrally as is the case in other vertebrates. Here we describe the topographical spread of cell differentiation for ganglion cells, double cones and rods in the zebrafish retina between 36 and 72 hours postfertilization (hpf), by using immunohistochemical markers in retinal wholemounts. Staining for all three cell types commenced within the ventral retina on the nasal side of the optic nerve and choroid fissure, at 38 hpf for ganglion cells and 50 hpf for double cones and rods. Within 3 to 4 hours, the staining of ganglion cells and double cones spread in a continuous wave-like fashion into the nasal region of the ventral retina. After this time, the staining patterns for ganglion cells and double cones progressed dorsally into the central and temporal retina. Finally, stained somata of ganglion cells were observed within the temporal-ventral region by approximately 48 hpf, more than 8 hours later than the first ganglion cells within the nasal retina. The topographical spread of double cone staining was slightly less orderly. After staining had extended into the nasal retina between 50 and 54 hpf, a small group of stained double cones often appeared at the temporal edge of the choroid fissure by 56 hpf, simultaneously with initial staining observed dorsal and temporal to the optic nerve. The topographical spread of rod staining in the ventral retina was more symmetrical. After rod staining appeared near the nasal edge of the choroid fissure at 50 hpf, rods accumulated within a localized patch nasal to the fissure. Approximately 5 hours after initial rod staining, scattered rod staining appeared on the temporal side of the choroid fissure (approximately 55-57 hpf). Rods increased rapidly within the ventral retina, and a dense symmetrical patch extended out from the choroid fissure into the nasal and temporal regions of the ventral retina by 70 hpf. A scattered pattern of rod staining also occurred within the dorsal retina at this time.
早期研究表明,斑马鱼的视网膜分化起始于腹侧而非中央,这与其他脊椎动物的情况不同。在此,我们通过对视网膜整装标本使用免疫组化标记物,描述了受精后36至72小时(hpf)斑马鱼视网膜中神经节细胞、双锥体细胞和视杆细胞的细胞分化的拓扑分布。所有这三种细胞类型的染色均起始于视神经和脉络膜裂鼻侧的腹侧视网膜,神经节细胞在38 hpf开始染色,双锥体细胞和视杆细胞在50 hpf开始染色。在3至4小时内,神经节细胞和双锥体细胞的染色以连续的波浪状方式扩散到腹侧视网膜的鼻侧区域。此后,神经节细胞和双锥体细胞的染色模式向背侧发展,进入中央和颞侧视网膜。最终,在大约48 hpf时,在颞腹侧区域观察到神经节细胞的染色胞体,比鼻侧视网膜中最早的神经节细胞晚8个多小时。双锥体细胞染色的拓扑分布稍欠有序。在50至54 hpf染色扩展到鼻侧视网膜后,到56 hpf时,一小群染色的双锥体细胞常常出现在脉络膜裂的颞侧边缘,同时在视神经的背侧和颞侧观察到初始染色。腹侧视网膜中视杆细胞染色的拓扑分布更为对称。在50 hpf视杆细胞染色出现在脉络膜裂鼻侧边缘附近后,视杆细胞在裂孔鼻侧的局部区域聚集。初始视杆细胞染色约5小时后,在脉络膜裂的颞侧出现散在的视杆细胞染色(约55 - 57 hpf)。视杆细胞在腹侧视网膜中迅速增加,到70 hpf时,一个密集对称的区域从脉络膜裂延伸到腹侧视网膜的鼻侧和颞侧区域。此时在背侧视网膜中也出现了散在的视杆细胞染色模式。