Niederländer C, Lumsden A
Department of Developmental Neurobiology, UMDS Guy's Hospital, London, UK.
Development. 1996 Aug;122(8):2367-74. doi: 10.1242/dev.122.8.2367.
Morphological segmentation of the avian hindbrain into rhombomeres is also reflected by the emergent organisation of branchiomotor nerves. In each case, the motor neurons of these nerves lie in two adjacent rhombomeres (e.g. of the Vth nerve in r2 and r3, VIIth in r4 and r5 etc.), and their outgrowing axons emerge into the periphery through defined exit points in rhombomeres r2, r4 and r6, respectively. Sensory axons of the cranial ganglia also enter the neuroepithelium at the same points. Motor axon outgrowth through experimentally rotated rhombomeres has suggested that a chemoattractive mechanism, involving the exit points, may form a component of their guidance. Yet so far, nothing is known about the establishment of the exit points or the identity of the cells that form them. In this study, we describe a group of late emigrating cranial neural crest cells which populate specifically the prospective exit points. Using chimaeras in which premigratory chick neural crest had been replaced orthotopically by quail cells, a population of neural crest was found to leave the cranial neural tube from about stage 10+ onwards and to migrate directly to the prospective exit points. These cells define the exit points by stage 12+, long before either motor or sensory axons have grown through them. The entire neural crest population of exit point cells expresses the recently described cell adhesion molecule c-cad7. Further, heterotopic grafting experiments show that midbrain and spinal cord crest, grafted at late stages in place of r4 crest, share the same migratory behaviour to the facial nerve exit points and express the same markers as cells contributed by the native r4 crest. It was not possible to generate new exit points in odd numbered rhombomeres simply by experimentally increasing their (normally insignificant) amount of crest production. Initiation of the exit point region probably lies, therefore, in the neuroepithelium.
鸟类后脑形态学上分割为菱脑节,这也反映在鳃运动神经的出现模式上。在每种情况下,这些神经的运动神经元位于两个相邻的菱脑节中(例如,三叉神经的运动神经元位于r2和r3,面神经的位于r4和r5等),它们生长的轴突分别通过菱脑节r2、r4和r6中特定的出口点进入外周。脑神经节的感觉轴突也在相同的点进入神经上皮。通过实验旋转菱脑节的运动轴突生长表明,涉及出口点的化学吸引机制可能是其导向的一个组成部分。然而,到目前为止,关于出口点的建立或形成它们的细胞的身份一无所知。在本研究中,我们描述了一组晚期迁出的脑神经嵴细胞,它们专门聚集在预期的出口点。使用将迁移前的鸡神经嵴原位替换为鹌鹑细胞的嵌合体,发现一群神经嵴细胞从大约10+期开始离开颅神经管,并直接迁移到预期的出口点。这些细胞在12+期之前就确定了出口点,远远早于运动或感觉轴突穿过它们。出口点细胞的整个神经嵴群体表达最近描述的细胞粘附分子c-cad7。此外,异位移植实验表明,在晚期移植到r4嵴位置的中脑和脊髓嵴,与面神经出口点具有相同的迁移行为,并表达与天然r4嵴贡献的细胞相同的标记。仅仅通过实验性增加奇数菱脑节(通常数量很少)的嵴产生量,不可能产生新的出口点。因此,出口点区域的起始可能位于神经上皮中。