Krushel L A, van der Kooy D
Department of Anatomy, University of Toronto, Ontario, Canada.
Dev Biol. 1993 Jul;158(1):145-62. doi: 10.1006/dbio.1993.1175.
The mammalian cerebral cortex and striatum exhibit spatially restricted distributions of neurons. These neuronal collectives correlate with the age at which the neurons become postmitotic. We investigated in vitro the role of cell adhesion in the organization of like-birthdated neurons within the rat telencephalon. Specifically, the ability of neurons of similar birthdate to reassociate with one another within either striatal or cortical reaggregates was observed. Early postmitotic neurons (destined for the striatal patch compartment and cortical deep layers) or later born neurons (destined for the striatal matrix compartment and cortical superficial layers) were labeled in vivo with [3H]-thymidine or bromodeoxyuridine (Brdu) on Embryonic Day (E) 13 or 18, respectively. Two or seven days later, the striatum and cortex were separately removed, dissociated, and reaggregated in suspension cultures for 5 days. Within both striatal and cortical reaggregates, E13 [3H]thymidine-labeled cells were observed to clump together toward the center of the reaggregates. Conversely, reaggregates containing cells labeled on E18 with a single [3H]thymidine injection or with two separate Brdu injections contained labeled cells which were dispersed with respect to each other, but showed an overall distribution toward the periphery of the reaggregates. These results suggest that early, but not late, postmitotic striatal and cortical neurons selectively associate with one another within their respective structures. Dissociated embryonic striatal and cortical neurons were then co-reaggregated to examine if a single adhesive mechanism is shared by both tissues. Early born neurons within these reaggregates clustered with each other regardless of tissue type. Later born cortical and striatal neurons were found dispersed in relation to each other and the early born neurons. However, the selective adhesion of early born striatal and cortical neurons is not an attribute of all early postmitotic forebrain neurons, because dissociated early born septal-basal forebrain neurons were found dispersed within reaggregates of septal-basal forebrain tissue or when cocultured with striatal tissue. These results suggest that the organization of cortical and striatal neuronal groups may depend on a common adhesive mechanism that crosses tissue-type boundaries.
哺乳动物的大脑皮层和纹状体呈现出神经元的空间受限分布。这些神经元集群与神经元进入有丝分裂后期的年龄相关。我们在体外研究了细胞黏附在大鼠端脑内出生时间相近的神经元组织中的作用。具体而言,观察了出生时间相近的神经元在纹状体或皮质再聚集物中彼此重新结合的能力。在胚胎第13天或第18天,分别用[³H] - 胸腺嘧啶核苷或溴脱氧尿苷(Brdu)在体内标记早期有丝分裂后期神经元( destined for the striatal patch compartment and cortical deep layers)或较晚出生的神经元( destined for the striatal matrix compartment and cortical superficial layers)。两天或七天后,分别取出纹状体和皮层,解离并在悬浮培养中重新聚集5天。在纹状体和皮质再聚集物中,观察到胚胎第13天用[³H] - 胸腺嘧啶核苷标记的细胞聚集在再聚集物的中心。相反,含有在胚胎第18天用单次[³H] - 胸腺嘧啶核苷注射或两次单独的Brdu注射标记的细胞的再聚集物,其标记细胞彼此分散,但总体上分布在再聚集物的周边。这些结果表明,有丝分裂后期早期而非晚期的纹状体和皮质神经元在其各自结构内选择性地彼此结合。然后将解离的胚胎纹状体和皮质神经元共同重新聚集,以检查这两种组织是否共享单一的黏附机制。这些再聚集物中的早期出生神经元无论组织类型如何都彼此聚集。发现较晚出生的皮质和纹状体神经元彼此分散,并且与早期出生的神经元分散。然而,早期出生的纹状体和皮质神经元的选择性黏附并非所有早期有丝分裂后期前脑神经元的特性,因为发现解离的早期出生的隔区 - 基底前脑神经元分散在隔区 - 基底前脑组织再聚集物内或与纹状体组织共培养时。这些结果表明,皮质和纹状体神经元群的组织可能依赖于跨越组织类型边界的共同黏附机制。 (注:原文中部分英文表述不太准确完整,翻译可能会稍显生硬,但尽量忠实于原文进行了翻译。)