Gaillard A, Gaillard F, Roger M
UMR 6558 Fac. Sciences, Département des Neurosciences, Université de Poitiers, Poitiers.
Adv Anat Embryol Cell Biol. 1998;148:1-86. doi: 10.1007/978-3-642-72179-3.
This report presents the results of neural transplantation experiments that were designed either to study neural developmental phenomena or to appraise the possible restorative capacity of grafts. The first part of the report deals with the findings of transplantation studies that were performed in newborn recipient rats in an attempt to determine the importance of extrinsic or intrinsic factors in the process of areal cortical differentiation. More precisely, we examined the extent to which extrinsic signals drive the pattern of efferent connections of neurons residing in different cortical areas. In the first experiment, we examined the general distribution pattern of efferents arising from homotopic as compared to heterotopic transplants of embryonic cortical tissue placed into the frontal cortex of newborn rats. Our findings indicated that embryonic occipital neurons transplanted heterotopically into the sensorimotor cortex: (a) only rarely contacted normal targets of the motor cortex, (b) systematically projected towards normal targets of the visual cortex, and (c) distributed fibers to structures normally receiving fibers from both the motor and visual cortex, either exclusively into the visual corticorecipient zone of the structure or into both the visual and motor corticorecipient zones. In the second experiment, we attempted to assess the densities of the spinal projections arising from homotopic or heterotopic transplants implanted into the frontal or occipital cortex of newborn rats. We provided evidence that transplants of embryonic neocortical neurons of frontal origin developed and maintained a spinal cord projection whatever their rostrocaudal position within the host neocortex, whereas transplants of occipital origin did not maintain a significant spinal cord projection in adulthood. Finally, in the third experiment, we analyzed the laminar and tangential distribution of the tectal projections developed by transplants of embryonic occipital cortex placed into the primary or secondary subdivisions of the occipital cortex of newborn rats. Abnormalities in the laminar and/or tangential organization of the tectal distribution of the transplant efferents were systematically found. Using these different transplantation paradigms, we provided increasing evidence that, in their heterotopic location, the embryonic neurons retain some of the developmental characteristics corresponding to their embryonic cortical site of origin. Our findings strongly suggested, therefore, that there is an early specification of neocortical neurons to develop area-specific efferents. In conclusion, converging lines of evidence suggest that regional differences in the neuroepithelium are predetermined early in development, thus leading to cerebral cortex parcellation, as hypothesized by Rakic (1988). In the second part of the report, we describe the results of a series of experiments dealing with the consequences of grafting embryonic cortex into the damaged cortex of adult rats. These effects were examined from an anatomical, metabolic, behavioral, and electrophysiological point of views. The experiments were conducted using either the frontal or the visual cortex as models to appraise the functional integration of the grafts into the motor or visual circuits, respectively. The first study was undertaken to examine the capacity of transplants of embryonic frontal neocortical tissue placed into the frontal cortex of an adult recipient to develop efferents into the host CNS. The results indicated that transplants of fetal neocortex placed into adult CNS had the capacity to develop efferents which seemed to grow over significant distances within the host corpus callosum but, in most cases, failed to penetrate deeply into the gray matter. The density of the efferent projections was, however, far weaker than that seen in newborn hosts. In the second study, the 2-deoxyglucose (2-DG) technique was used to examine the functional integration of hom
本报告展示了神经移植实验的结果,这些实验旨在研究神经发育现象或评估移植可能的修复能力。报告的第一部分涉及在新生受体大鼠中进行的移植研究结果,以试图确定外在或内在因素在区域皮质分化过程中的重要性。更确切地说,我们研究了外在信号驱动不同皮质区域神经元传出连接模式的程度。在第一个实验中,我们研究了与植入新生大鼠额叶皮质的胚胎皮质组织异位移植相比,同源移植产生的传出纤维的总体分布模式。我们的研究结果表明,异位移植到感觉运动皮质的胚胎枕叶神经元:(a) 很少与运动皮质的正常靶标接触,(b) 系统地投射到视觉皮质的正常靶标,并且 (c) 将纤维分布到通常从运动和视觉皮质接收纤维的结构,要么仅进入该结构的视觉皮质接受区,要么进入视觉和运动皮质接受区。在第二个实验中,我们试图评估植入新生大鼠额叶或枕叶皮质的同源或异位移植产生的脊髓投射密度。我们提供的证据表明,额叶起源的胚胎新皮质神经元移植无论在宿主新皮质内的头尾位置如何,都能发育并维持脊髓投射,而枕叶起源的移植在成年期则不能维持显著的脊髓投射。最后,在第三个实验中,我们分析了植入新生大鼠枕叶皮质初级或次级分区的胚胎枕叶皮质移植产生的顶盖投射的层状和切线分布。系统地发现了移植传出纤维顶盖分布的层状和/或切线组织异常。使用这些不同的移植范式,我们提供了越来越多的证据表明,在异位位置,胚胎神经元保留了一些与其胚胎皮质起源部位相对应的发育特征。因此,我们的研究结果强烈表明,新皮质神经元在早期就被指定发展区域特异性传出纤维。总之,越来越多的证据表明,神经上皮的区域差异在发育早期就已预先确定,从而导致大脑皮质分区,正如拉基奇(1988年)所假设的那样。在报告的第二部分,我们描述了一系列实验的结果,这些实验涉及将胚胎皮质移植到成年大鼠受损皮质的后果。从解剖学、代谢、行为和电生理学角度检查了这些影响。使用额叶或视觉皮质作为模型进行实验,分别评估移植到运动或视觉回路中的功能整合。第一项研究旨在检查植入成年受体额叶皮质的胚胎额叶新皮质组织移植向宿主中枢神经系统发展传出纤维的能力。结果表明,植入成年中枢神经系统的胎儿新皮质移植有能力发展传出纤维,这些纤维似乎在宿主胼胝体内远距离生长,但在大多数情况下,未能深入穿透灰质。然而,传出投射的密度远低于在新生宿主中看到的密度。在第二项研究中,使用2-脱氧葡萄糖(2-DG)技术检查同源……