Marotte L R
Developmental Neurobiology Group, Research School of Biological Sciences, Australian National University, Canberra.
J Comp Neurol. 1993 May 1;331(1):1-13. doi: 10.1002/cne.903310102.
The position of ganglion cells contributing to the early imprecision in retinotopic order in the developing retinocollicular projection in the wallaby (Macropus eugenii) has been determined. Deposits of horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP) were made in the caudal pole of the superior colliculus (SC) at ages ranging from 22 days after birth, when sparse retinal axons have only just reached the caudal pole of the SC and are yet to cover its surface completely, to 96 days when the retinotopy of ganglion cell terminals in the SC is precise (Marotte, '90). From 30 days onwards, the deposit of WGA-HRP resulted in a dense patch of retrogradely labelled retinal ganglion cells that could be seen to be appropriately positioned in nasal retina. However, at all ages prior to 92 days, there were inappropriately positioned labelled cells between the densely labelled patch and the central retina and both dorsal and ventral to the patch. They were not found in far distant regions of retina and composed a relatively small proportion of labelled cells. They reached a peak at 45 days, had decreased to low levels by 63 days, were rare by 81 days, and by 92 days were absent. This latter age fits with the time when retinotopy was judged to be precise in a previous study (Marotte, '90). Inappropriately projecting cells never originate from the entire retina but only from regions adjacent to the appropriate region. Thus, during development there are no gross projection errors. Initially, ganglion cell axons are distributed on the colliculus in a coarse retinotopy. Refinement of the projection then follows, revealed by this technique as a loss of inappropriately projecting ganglion cells. This is complete by 92 days well before eye opening at around 140 days.
已确定了在沙袋鼠(尤金袋鼠)发育中的视网膜 - 丘脑投射中,导致视网膜拓扑顺序早期不精确的神经节细胞的位置。将与小麦胚凝集素结合的辣根过氧化物酶(WGA - HRP)注射到上丘(SC)的尾极,注射时间从出生后22天开始,此时稀疏的视网膜轴突刚刚到达SC的尾极且尚未完全覆盖其表面,一直到96天,此时SC中神经节细胞终末的视网膜拓扑定位是精确的(Marotte,1990年)。从30天起,WGA - HRP的注射导致密集的逆行标记视网膜神经节细胞斑块,可观察到这些细胞在鼻侧视网膜中位置恰当。然而,在92天之前的所有年龄段,在密集标记斑块与中央视网膜之间以及斑块的背侧和腹侧都存在位置不当的标记细胞。它们在视网膜的远处区域未被发现,且在标记细胞中占比较小。它们在45天达到峰值,到63天降至低水平,81天时很少见,到92天时消失。后一个年龄与之前一项研究中判断视网膜拓扑定位精确的时间相符(Marotte,1990年)。投射不当的细胞并非起源于整个视网膜,而是仅来自与恰当区域相邻的区域。因此,在发育过程中不存在严重的投射错误。最初,神经节细胞轴突以粗略的视网膜拓扑分布在上丘上。随后投射得到细化,通过这项技术可表现为投射不当的神经节细胞减少。到92天时这种细化完成,远早于约140天睁眼的时间。