Horsburgh G M, Sefton A J
Department of Physiology, University of Sydney, New South Wales, Australia.
J Comp Neurol. 1987 Sep 22;263(4):553-66. doi: 10.1002/cne.902630407.
We have investigated the time course and magnitude of cellular degeneration in the ganglion cell layer and the presumptive amacrine and bipolar regions of the inner nuclear layer during the development of the retina in the rat. Pyknotic profiles are present in the ganglion cell layer during the first 2 postnatal weeks, reaching peak numbers during the first 4 postnatal days (corresponding to the time of greatest loss of ganglion cells and their axons: Potts et al., '82; Lam et al., '82; Perry et al., '83). Two observations suggest that the majority of pyknotic profiles present in the ganglion cell layer during the second postnatal week are not ganglion cells. First, following injection of kainic acid into one superior colliculus, degenerating ganglion cells in the contralateral retina are cleared within 24-48 hours. Therefore, since most ganglion cell and axon loss occurs within the first postnatal week, few of the pyknotic profiles present in the second week are likely to be ganglion cells. Second, the time course of cellular degeneration in the ganglion cell layer during the second postnatal week follows a very similar pattern to that seen in the presumptive amacrine sublayer of the inner nuclear layer. Such a correspondence suggests that two phases of cell death occur in the ganglion cell layer: during the first postnatal week the majority of dying cells are ganglion cells, and in the second, most cell death is due to a loss of displaced amacrine cells. In the inner nuclear layer pyknotic profiles are most numerous in the presumptive amacrine region on postnatal days 6 and 7, and in the presumptive bipolar region on day 10. Synaptogenesis in the inner plexiform layer occurs later but reflects the order of cell death. Thus, conventional (presumed amacrine) synapses were first observed on day 11 and synaptic ribbons (indicative of bipolar synapses) on day 13. These observations suggest that amacrine and bipolar cells initiate synapses only after their numbers have stabilized.
我们研究了大鼠视网膜发育过程中神经节细胞层以及内核层假定无长突细胞和双极细胞区域细胞变性的时间进程和程度。在出生后的前两周,神经节细胞层中存在固缩核轮廓,在出生后的前4天达到峰值数量(这与神经节细胞及其轴突大量丧失的时间相对应:Potts等人,1982年;Lam等人,1982年;Perry等人,1983年)。两项观察结果表明,出生后第二周神经节细胞层中存在的大多数固缩核轮廓并非神经节细胞。第一,向一侧上丘注射海人酸后,对侧视网膜中退化的神经节细胞在24 - 48小时内清除。因此,由于大多数神经节细胞和轴突丧失发生在出生后的第一周,第二周出现的固缩核轮廓中很少可能是神经节细胞。第二,出生后第二周神经节细胞层中细胞变性的时间进程与内核层假定无长突细胞亚层中观察到的模式非常相似。这种对应关系表明神经节细胞层中发生了两个细胞死亡阶段:在出生后的第一周,大多数死亡细胞是神经节细胞,而在第二周,大多数细胞死亡是由于移位无长突细胞的丧失。在内核层,固缩核轮廓在出生后第6天和第7天在假定无长突细胞区域最多,在第10天在假定双极细胞区域最多。内网状层的突触形成较晚,但反映了细胞死亡的顺序。因此,传统的(假定无长突细胞的)突触在第11天首次观察到,突触带(指示双极突触)在第13天观察到。这些观察结果表明,无长突细胞和双极细胞只有在其数量稳定后才开始形成突触。