Auladell C, Martinez A, Alcantara S, Supèr H, Soriano E
Unit of Cell Biology, Faculty of Biology, University of Barcelona, Spain.
Neuroscience. 1995 Feb;64(4):1091-103. doi: 10.1016/0306-4522(94)00393-j.
The presence of migrating callosal neurons during the development of the murine cerebral cortex was studied using biocytin and the lipophilic dye, 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate as retrograde tracers. After injections of biocytin in the presumptive somatosensory cortex of newborn mice which were analysed one day later, many anterogradely labelled fibres coursed towards the contralateral hemisphere through the corpus callosum. Retrogradely labelled callosal cells were also observed. Most callosal neurons corresponded to immature pyramidal cells. In addition, a few biocytin-labelled callosal neurons displayed extremely fusiform shapes, vertical orientation and a short, single process emerging from the apical side of the perikaryon. At the electron microscopic level, these cells had features identical to those described for migrating callosal neurons. Twenty-four hours after birth, these migrating neurons were almost exclusively observed in the upper, dense aspect of the cortical plate (presumptive layers II-III) and only very exceptionally in the infragranular layers. No retrogradely labelled cell resembling migrating neurons were noticed after injections on postnatal days 2 or 5. To study migrating callosal neurons at embryonic stages, crystals of the lipophilic dye were injected in the corpus callosum or the contralateral white matter in embryos aged 17, 18 and 19 days, corresponding to the initial development of the corpus callosum in mice. Whereas callosal migrating neurons were not detected at embryonic days 17 and 18, injections of the lipophilic dye on embryonic day 19 revealed the presence of labelled migrating neurons in the infragranular layers. To corroborate further that these cells are migrating neurons, [3H]thymidine was administered on embryonic days 16 and 17, and labelled mice were injected with biocytin on embryonic day 19 or the first postnatal day. Retrogradely labelled callosal neurons resembling migrating neurons were autoradiographically labelled. These results indicate that the specification of certain neuronal types and the emergence of their cell type-specific characteristics occur shortly after postmitotic neurons leave the ventricular zone, before being positioned within the cortical plate.
利用生物胞素和脂溶性染料1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐作为逆行示踪剂,研究了小鼠大脑皮质发育过程中胼胝体迁移神经元的存在情况。在新生小鼠的体感皮质假定区注射生物胞素,一天后进行分析,许多顺行标记的纤维通过胼胝体向对侧半球延伸。还观察到逆行标记的胼胝体细胞。大多数胼胝体神经元对应于未成熟的锥体细胞。此外,一些生物胞素标记的胼胝体神经元呈现出极细长的形状、垂直的方向以及从胞体顶端发出的短而单一的突起。在电子显微镜水平上,这些细胞具有与描述的迁移胼胝体神经元相同的特征。出生后24小时,这些迁移神经元几乎只在皮质板的上部致密区域(假定的II - III层)被观察到,在颗粒下层中极少见到。在出生后第2天或第5天注射后,未发现类似迁移神经元的逆行标记细胞。为了研究胚胎期的迁移胼胝体神经元,将脂溶性染料晶体注射到17、18和19天龄胚胎的胼胝体或对侧白质中,这与小鼠胼胝体的初始发育阶段相对应。在胚胎第17天和18天未检测到胼胝体迁移神经元,而在胚胎第19天注射脂溶性染料显示颗粒下层存在标记的迁移神经元。为了进一步证实这些细胞是迁移神经元,在胚胎第16天和17天给予[³H]胸腺嘧啶核苷,并在胚胎第19天或出生后第一天给标记的小鼠注射生物胞素。类似迁移神经元的逆行标记胼胝体神经元被放射自显影标记。这些结果表明,某些神经元类型的特化及其细胞类型特异性特征的出现发生在有丝分裂后神经元离开脑室区后不久,在它们定位到皮质板之前。