Polleux F, Dehay C, Kennedy H
INSERM U371-Cerveau et Vision, Bron, France.
J Comp Neurol. 1997 Aug 18;385(1):95-116.
In the primate visual cortex, the birthdate of neurons in homologous layers differ on either side of the 17-18 border suggesting that there might be different timetables of laminar histogenesis in these two areas (Dehay et al. [1993] Nature 366:464-466 and Kennedy et al. [1996] Soc. Neurosci. Abst. 22:525). Because of the potential importance of these findings for understanding mechanisms that generate areal identity, we have developed an experimental approach that makes it possible to accurately compute the timetable of laminar histogenesis from birthdating experiments. Here we report the results of an exhaustive examination of the tempo of layer production in five cortical areas of the mouse. Tritiated thymidine pulse injections were made during embryonic development and labeled neurons were examined in three frontoparietal areas (areas 3, 4, and 6) and two occipital areas (areas 17 and 18a) of the adult cortex. The correlation between the radial distribution of neurons and the intensities of labeling enabled us to reliably identify first generation neurons (i.e., those neurons that quit the cell-cycle in the first round of mitosis after injection). For each cortical layer, the percentage of first generation neurons with respect to the total number of neurons defined a laminar labeling index. Changes of the laminar labeling index over time determined the timetable of layer formation. The onset and duration of layer formation was identical in the two occipital areas. This finding contrasted with the frontoparietal areas where there were important differences in the timing of infragranular and granular layer formation and noticeably production of layers VIa, V, and IV occurs earlier in area 3 than in area 6. The timing of laminar production of areas 17 and 18a resembles more that of area 3 than that of area 6. With respect to areas 3 and 6, area 4 shows an intermediate but significantly different timetable of layer production. These marked areal differences in the timetable of laminar histogenesis contrasted with the relative homogeneity within areas so that we have been able to demonstrate that the interareal differences are not merely the expression of known neurogenic gradients. These results suggest that in the mouse frontoparietal isocortex, neighbouring regions of the ventricular zone that will give rise to distinct areas follow distinct programs of layer production. These areal differences occur before thalamic innervation and suggest an early regionalisation of laminar histogenesis.
在灵长类动物的视觉皮层中,17-18区边界两侧同源层中神经元的出生日期不同,这表明这两个区域可能存在不同的层状组织发生时间表(德海等人[1993]《自然》366:464-466;肯尼迪等人[1996]《神经科学学会文摘》22:525)。鉴于这些发现对于理解产生区域特性的机制具有潜在重要性,我们开发了一种实验方法,能够根据出生日期实验准确计算层状组织发生的时间表。在此,我们报告了对小鼠五个皮质区域层形成节奏进行详尽研究的结果。在胚胎发育期间进行了氚标记胸腺嘧啶脉冲注射,并在成年皮质的三个额顶叶区域(3区、4区和6区)以及两个枕叶区域(17区和18a区)检查了标记的神经元。神经元的径向分布与标记强度之间的相关性使我们能够可靠地识别第一代神经元(即那些在注射后第一轮有丝分裂中退出细胞周期的神经元)。对于每个皮质层,第一代神经元相对于神经元总数的百分比定义了层状标记指数。层状标记指数随时间的变化确定了层形成的时间表。两个枕叶区域层形成的起始和持续时间相同。这一发现与额顶叶区域形成对比,在额顶叶区域,颗粒下层和颗粒层形成的时间存在重要差异,并且明显地,6层a、5层和4层在3区的产生早于6区。17区和18a区的层状产生时间更类似于3区而非6区。相对于3区和6区,4区显示出中间但明显不同的层产生时间表。层状组织发生时间表中这些显著的区域差异与区域内的相对同质性形成对比,因此我们能够证明区域间差异不仅仅是已知神经源性梯度的表现。这些结果表明,在小鼠额顶叶等皮质中,将产生不同区域的脑室区相邻区域遵循不同的层产生程序。这些区域差异在丘脑神经支配之前就已出现,表明层状组织发生存在早期区域化。