Departamento de Anatomía, Facultad de Medicina, Universidad de La Laguna, Tenerife, Spain.
J Anat. 2010 Oct;217(4):334-43. doi: 10.1111/j.1469-7580.2010.01266.x.
Cajal-Retzius (CR) cells are the most significant source of reelin, an extracellular matrix glycoprotein essential for cortical development. Strategically located in the marginal zone, CR cells control radial migration and laminar positioning of pyramidal neurons of the cortical plate. They degenerate and undergo cell death when cortical migration is completed. In human cortex development, reelin-expressing CR cells are already present in the early preplate, and continue to increase in number after the appearance of the cortical plate. In the course of the first half of gestation, the reelin signal in the marginal zone undergoes a huge amplification in parallel with the growth of the cortical plate and the expansion of the cortical surface. A significant source of CR cells is the cortical hem, a putative signalling centre at the interface of the prospective hippocampus and the choroid plexus. Hem-derived CR cells co-express reelin and p73, a transcription factor of the p53-family. They form the predominant CR cell population of the human neocortex. Characteristically, CR cells express the anti-apoptotic isoform DeltaNp73 which may be responsible for the protracted lifespan of human CR cells and the morphological differentiation of their axonal plexus. This dense fibre plexus, absent in lower mammals, amplifies the reelin-signal and establishes a physical boundary between the cortical plate and the marginal zone. In this review, we analyze the multiple sources of reelin/p73 positive CR cells at the interface of various telencephalic centres and the choroid plexus of the lateral ventricles. Additional populations of CR cells may derive from the thalamic eminence in the ventral thalamus and from the strionuclear neuroepithelium, or 'amygdalar hem'. Comparative studies in a variety of species indicate that the cortical hem is the main origin of CR cells destined for the neocortex, and is most highly developed in the human brain. The close association between cortical hem and choroid plexus suggests a concerted role in the evolutionary increase of CR cells, amplification of the reelin signal in the marginal zone, and cortical expansion.
Cajal-Retzius (CR) 细胞是 reelin 的最重要来源,reelin 是一种细胞外基质糖蛋白,对皮质发育至关重要。CR 细胞位于边缘区,可控制皮质板的放射状迁移和层状定位。当皮质迁移完成时,它们会退化并死亡。在人类皮质发育过程中,表达 reelin 的 CR 细胞已经存在于早期的基板中,并且在皮质板出现后数量继续增加。在妊娠的前半段,边缘区的 reelin 信号与皮质板的生长和皮质表面的扩展同时发生巨大扩增。CR 细胞的一个重要来源是皮质 hem,它是潜在的海马和脉络丛之间的信号中心。源自 hem 的 CR 细胞共同表达 reelin 和 p73,p73 是 p53 家族的转录因子。它们形成人类新皮质的主要 CR 细胞群体。特征性地,CR 细胞表达抗凋亡同工型 DeltaNp73,这可能是人类 CR 细胞寿命延长和其轴突丛形态分化的原因。这种密集的纤维丛在较低的哺乳动物中不存在,它增强了 reelin 信号,并在皮质板和边缘区之间建立了物理边界。在这篇综述中,我们分析了各种端脑中心和侧脑室脉络丛界面处的 reelin/p73 阳性 CR 细胞的多个来源。CR 细胞的其他群体可能源自腹侧丘脑的丘脑隆起和纹状神经上皮或“杏仁核 hem”。在各种物种中的比较研究表明,皮质 hem 是皮质 hem 的主要来源,是新皮质的起源,在人类大脑中发育最为发达。皮质 hem 与脉络丛的密切关联表明它们在 CR 细胞的协同作用,边缘区 reelin 信号的放大和皮质扩张。