Clarke P G
J Comp Neurol. 1982 May 20;207(3):208-22. doi: 10.1002/cne.902070303.
By thymidine autoradiography it is shown that the entire isthmic complex is arranged according to a single and very finely grained gradient of proliferation that manifests itself in each of the component cell groups individually. Ventral neurons are generated first, dorsal last. The neurons in the various isthmic cell groups complete their final phase of DNA synthesis mainly between the following stages (of Hamburger and Hamilton, '51): N. semilunaris, HH-22 to HH-24; N. lemnisci lateralis pars ventralis, HH-23 to HH-25; N. lemnisci lateralis pars dorsalis, HH-24 to HH-27; N. isthmi partes principales magnocellularis and parvocellularis, HH-24 to HH-29; N. isthmo-opticus, HH-27 to HH-31. By thymidine autoradiography combined with the peroxidase retrograde transport technique, it is shown that the retinopetal neurons ventral to N. isthmo-optic neurons and substantially later than the nonretinopetal neurons amongst which they are scattered. Using similar autoradiographic methods but in embryos fixed at various ages, it is then shown that the isthmic alar plate gives rise to all the cell groups of the isthmic complex except possibly N. isthmi pars principalis magnocellularis. In confirmation of Vaage's ('73) account, it is shown that two main migrations, "dorsal" and dorsolateral", orignate from the dorsal and dorsolateral parts of the germinal epithelium, traveling first laterally and then ventrally, and that some cells from the former subsequently join the latter to create the mixed migration. The dorsal migration gives rise to N. semilunaris, N. isthmi pars principalis parvocellularis and N. isthmo-opticus, whereas the mixed gives rise to N. lemnisci lateralis partes dorsalis and ventralis and to much of the adjacent reticular formation. The migration is extremely rapid (15-30 micrometer per hour for the dorsal migration), but much of this speed may be due to passive bulk displacement, since there seems to be little relative movement between adjacent cells.
通过胸腺嘧啶核苷放射自显影法表明,整个峡部复合体是按照单一且非常精细的增殖梯度排列的,这种梯度在每个组成细胞群中都有单独体现。腹侧神经元最先产生,背侧神经元最后产生。不同峡部细胞群中的神经元主要在以下阶段(根据汉堡和汉密尔顿,1951年)之间完成其DNA合成的最后阶段:半月神经节,HH - 22至HH - 24;外侧丘系腹侧部神经,HH - 23至HH - 25;外侧丘系背侧部神经,HH - 24至HH - 27;峡部主大细胞部和小细胞部神经,HH - 24至HH - 29;峡视神经,HH - 27至HH - 31。通过将胸腺嘧啶核苷放射自显影法与过氧化物酶逆行运输技术相结合表明,峡视神经腹侧的视网膜向心性神经元的产生时间比它们所散布于其中的非视网膜向心性神经元晚得多。使用类似的放射自显影方法,但针对不同年龄固定的胚胎,结果表明峡部翼板产生了峡部复合体的所有细胞群,可能除了峡部主大细胞部神经。为了证实瓦格(1973年)的描述,研究表明有两种主要的迁移,即“背侧”和“背外侧”迁移,它们起源于生发上皮的背侧和背外侧部分,先向外侧然后向腹侧移动,并且前者的一些细胞随后加入后者形成混合迁移。背侧迁移产生半月神经节、峡部主小细胞部神经和峡视神经,而混合迁移产生外侧丘系背侧部和腹侧部神经以及大部分相邻的网状结构。这种迁移极其迅速(背侧迁移速度为每小时15 - 30微米),但这种速度很大程度上可能是由于被动的整体位移,因为相邻细胞之间似乎几乎没有相对运动。