Rakic P
UCLA Forum Med Sci. 1975(18):3-40. doi: 10.1016/b978-0-12-139050-1.50008-2.
The place and time of origin, the migration and eventual disposition of neurons of the monkey visual cortex were studied by autoradiography in animals killed at various intervals after 3H-thymidine pulse labeling at embryonic (E) and early postnatal (P) stages. All neurons destined for the visual cortex are generated during about a 2-month period between E45 and E102. Neuron position in the cortical laminae correlates systematically with time of cell origin; neurons destined for deeper cortical positions are generated earlier, and more superficial ones progressively later. Thus, most neurons in layer VI are born between E45 and E60, in layer V between E60 and E70, in layer IV between E70 and E80, and in layers III and II between E80 and E102. No neurons, but numerous glia, are generated within the cortical plate itself. Initially young neurons are produced almost exclusively in the ventricular zone. Later they are probably generated in both ventricular and subventricular zones, and by the end of the proliferative period the subventricular zone becomes the predominant source of new cells. At the time when all neurons destined for the monkey visual cortex have already been produced, primary fissures are barely indicated on the cerebral surface and no secondary fissure appears as yet. Autoradiographic analyses indicate that at early stages young neurons move to the cortical plate relatively synchronously and at a fast rate, whereas at later stages there are considerable differences in the rates of cell migration. At early stages when the migration pathway is relatively short, the external process of the ventricular cell may stretch across almost the entire migratory distance. It is possible that nuclei move without interruption within their own cylinders of cytoplasm, a mechanism which might account for the rapid, synchronous movement of cell bodies as seen in the autoradiographic material. During later stages when young neurons, mostly of subventricular origin, move across a distance which is more than 10 times the length of their leading process, migrating cells follow radial glial guides across the widened intermediate zone and through densely packed cortical plate. This type of cell displacement seems to proceed less synchronously and require more time. It is proposed that two different mechanisms of cell displacement might exist: one in operation at early stages of cortical formation when mostly ventricular cells migrate, and another utilized by subventricular cells at later stages.
通过放射自显影技术,对在胚胎期(E)和出生后早期(P)阶段经3H-胸腺嘧啶脉冲标记后,于不同时间间隔处死的动物进行研究,以确定猕猴视皮层神经元的起源地点和时间、迁移过程及最终归宿。所有注定要进入视皮层的神经元都是在E45至E102之间约2个月的时间内产生的。神经元在皮质板层中的位置与细胞起源时间有系统的相关性;注定要进入皮质较深层位置的神经元产生得较早,而较浅层的神经元则逐渐较晚产生。因此,VI层中的大多数神经元在E45至E60之间出生,V层在E60至E70之间,IV层在E70至E80之间,III层和II层在E80至E102之间。皮质板本身不产生神经元,但产生大量神经胶质细胞。最初,年轻神经元几乎完全在脑室区产生。后来它们可能在脑室区和脑室下区都有产生,到增殖期结束时,脑室下区成为新细胞的主要来源。当所有注定要进入猕猴视皮层的神经元都已产生时,大脑表面几乎还没有显示出初级沟,也还没有出现次级沟。放射自显影分析表明,在早期,年轻神经元相对同步且快速地迁移到皮质板,而在后期,细胞迁移速度存在相当大的差异。在早期,迁移路径相对较短,脑室细胞的外部突起可能几乎伸展到整个迁移距离。细胞核有可能在其自身的细胞质柱内不间断地移动,这种机制可能解释了放射自显影材料中所见的细胞体的快速、同步移动。在后期,大多数起源于脑室下区的年轻神经元要迁移的距离超过其领先突起长度的10倍,迁移的细胞沿着放射状胶质细胞的引导穿过变宽的中间区并穿过密集排列的皮质板。这种类型的细胞位移似乎进行得不太同步,需要更多时间。有人提出可能存在两种不同的细胞位移机制:一种在皮质形成的早期起作用,此时主要是脑室细胞迁移;另一种是脑室下细胞在后期使用的机制。