Altman J, Bayer S A
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.
J Comp Neurol. 1987 Mar 22;257(4):529-52. doi: 10.1002/cne.902570405.
Sequential thymidine radiograms from rats injected on days E16, E17, E18, and E19 and killed 2 hours after injection and at daily intervals up to day E22 were used to establish the site of origin, migratory route, and settling patterns of neurons of the nucleus reticularis tegmenti pontis and basal pontine gray. The nucleus reticularis tegmenti pontis neurons, which are produced predominantly on days E15 and E16, derive from the primary precerebellar neuroepithelium. These cells, unlike those of the lateral reticular and external cuneate nuclei, take an anteroventral subpial route, forming the anterior precerebellar extramural migratory stream. This migratory stream reaches the anterior pole of the pons by day E18. In rats injected on day E16 and killed on day E18 some of the cells that reach the pons are unlabeled, indicating that they represent the early component of neurons generated on day E15. The cells labeled on day E16 begin to settle in the pons on day E19, 3 days after their production. These cells, migrating in an orderly temporal sequence, form a posterodorsal-to-anteroventral gradient in the nucleus reticularis tegmenti pontis. Unlike the neurons of all the other precerebellar nuclei, the basal pontine gray neurons derive from the secondary precerebellar neuroepithelium. The secondary precerebellar neuroepithelium forms on day E16 as an outgrowth of the primary precerebellar neuroepithelium, and it remains mitotically active through day E19, spanning the entire period of basal pontine gray neurogenesis. The secondary precerebellar neuroepithelium is surrounded by a horizontal layer of postmitotic cells, representing the head-waters of the anterior precerebellar extramural migratory stream. In rats injected on day E18 and killed on day E19 the cells are labeled in the proximal half of the stream around the medulla but those closer to the pons are unlabeled, indicating an orderly sequence of migration. In rats injected on day E18 and killed on day E20 the labeled cells reach the pole of the pons. In the basal pontine gray the sequentially generated neurons settle in a precise order. The neurons generated on day E16 form a small core posteriorly and the neurons generated on days E17, E18, and E19 form regular concentric rings around the core in an inside-out sequence.
对在胚胎第16天、17天、18天和19天注射的大鼠进行连续的胸苷放射自显影片观察,这些大鼠在注射后2小时处死,并在之后每天处死直至胚胎第22天,以此来确定脑桥被盖网状核和脑桥基底灰质神经元的起源部位、迁移路径和定居模式。脑桥被盖网状核神经元主要在胚胎第15天和16天产生,源自初级小脑前神经上皮。与外侧网状核和楔外核的神经元不同,这些细胞采取前腹侧软膜下路径,形成小脑前壁外迁移流。到胚胎第18天,这个迁移流到达脑桥的前极。在胚胎第16天注射并在第18天处死的大鼠中,一些到达脑桥的细胞未被标记,这表明它们代表胚胎第15天产生的神经元的早期成分。胚胎第16天标记的细胞在产生3天后,即胚胎第19天开始在脑桥定居。这些细胞按有序的时间顺序迁移,在脑桥被盖网状核中形成从后背部到前腹侧的梯度。与所有其他小脑前核的神经元不同,脑桥基底灰质神经元源自次级小脑前神经上皮。次级小脑前神经上皮在胚胎第16天作为初级小脑前神经上皮的衍生物形成,并在胚胎第19天之前一直保持有丝分裂活性,贯穿脑桥基底灰质神经发生的整个时期。次级小脑前神经上皮被一层水平的有丝分裂后细胞包围,这些细胞代表小脑前壁外迁移流的源头。在胚胎第18天注射并在第19天处死的大鼠中,细胞在延髓周围迁移流的近端一半被标记,但靠近脑桥的细胞未被标记,这表明迁移顺序是有序的。在胚胎第18天注射并在第20天处死的大鼠中,标记的细胞到达脑桥极。在脑桥基底灰质中,依次产生的神经元按精确顺序定居。胚胎第16天产生的神经元在后部形成一个小核心,而胚胎第17天、18天和19天产生的神经元围绕该核心以由内向外的顺序形成规则的同心环。