Dehay C, Kennedy H, Bullier J
Laboratoire de Neuropsychologie Expérimentale, INSERM, unité 94, Bron, France.
J Comp Neurol. 1988 Jun 1;272(1):68-89. doi: 10.1002/cne.902720106.
We have examined the anatomical features of ipsilateral transient cortical projections to areas 17, 18, and 19 in the kitten with the use of axonal tracers Fast Blue and WGA-HRP. Injections of tracers in any of the three primary visual areas led to retrograde labeling in frontal, parietal, and temporal cortices. Retrogradely labeled cells were not randomly distributed, but instead occurred preferentially at certain loci. The pattern of retrograde labeling was not influenced by the area injected. The main locus of transiently projecting neurons was an isolated region in the ectosylvian gyrus, probably corresponding to auditory area A1. Other groups of transiently projecting neurons had more variable locations in the frontoparietal cortex. The laminar distribution of neurons sending a transient projection to the visual cortex is characteristic and different from that of parent neurons of other cortical pathways at the same age. In the frontoparietal cortex, transiently projecting neurons were located mainly in layer 1 and the upper part of layers 2 and 3. In the ectosylvian gyrus, nearly all the neurons are located in layers 2 and 3. In addition, a few transiently projecting neurons are found in layer 6 and in the white matter. Transiently projecting neurons have a pyramidal morphology except for the occasional spindle-shaped cell of layer 1 and multipolar cells observed in the white matter. Anterograde studies were used to investigate the location of transient fibers in the visual cortex. Injections of WGA-HRP at the site of origin of transient projections gave rise to few retrogradely labeled cells in areas 17, 18, and 19, demonstrating that transient projections to these areas are not reciprocal. Although labeled axons were found over a wide area of the posterior cortex, they were more numerous over certain regions, including areas 17, 18, and 19, and absent from other more lateral cortical regions. Transient projecting fibers were present in all cortical layers at birth. Plotting the location of transient fibers in numerous sections and at all ages showed that these fibers are not more plentiful in the white matter than they are in the gray matter. We found no evidence that the white/gray matter border constituted a physical barrier to the growth of transient axons. Comparison of the organization of this transient pathway to that of other transient connections is discussed with respect to the development of the cortex.
我们使用轴突示踪剂快蓝和WGA-HRP研究了小猫同侧到17、18和19区的短暂皮质投射的解剖学特征。在三个主要视觉区域中的任何一个注射示踪剂都会导致额叶、顶叶和颞叶皮质的逆行标记。逆行标记的细胞并非随机分布,而是优先出现在某些位点。逆行标记的模式不受注射区域的影响。短暂投射神经元的主要位点是外侧薛氏回中的一个孤立区域,可能对应于听觉区域A1。其他短暂投射神经元组在额顶叶皮质中的位置更具变异性。向视觉皮质发送短暂投射的神经元的层状分布具有特征性,与同年龄其他皮质通路的母神经元不同。在额顶叶皮质中,短暂投射神经元主要位于第1层以及第2和第3层的上部。在外侧薛氏回中,几乎所有神经元都位于第2和第3层。此外,在第6层和白质中发现了一些短暂投射神经元。除了第1层偶尔出现的纺锤形细胞和白质中观察到的多极细胞外,短暂投射神经元具有锥体形态。顺行研究用于研究视觉皮质中短暂纤维的位置。在短暂投射的起源部位注射WGA-HRP在17、18和19区产生了少量逆行标记的细胞,表明向这些区域的短暂投射不是相互的。尽管在后部皮质的广泛区域发现了标记的轴突,但在某些区域,包括17、18和19区,它们更多,而在其他更外侧的皮质区域则没有。出生时所有皮质层中都存在短暂投射纤维。绘制多个切片和所有年龄段中短暂纤维的位置表明,这些纤维在白质中并不比在灰质中更丰富。我们没有发现证据表明白质/灰质边界对短暂轴突的生长构成物理障碍。关于皮质的发育,讨论了该短暂通路与其他短暂连接的组织比较。