Tosney K W
Department of Biology, University of Michigan, Ann Arbor 48109.
Dev Biol. 1988 Jun;127(2):266-86. doi: 10.1016/0012-1606(88)90314-4.
The development of patterned axon outgrowth and dorsal root ganglion (DRG) formation was examined after partially or totally removing chick somitic mesoderm. Since the dermamyotome is not essential and a full complement of limb muscles developed, alterations in neural patterns could be ascribed to deletion of sclerotome. When somitic tissue was completely removed, axons extended and DRG formed, but in an unsegmented pattern. Therefore the somite does not elicit outgrowth of axons or migration of DRG precursors, it is not a manditory substratum and it is not required for DRG condensation. These results suggest that posterior sclerotome is relatively inhibitory to invasion, an inhibition that is released when sclerotome is absent. When somites were partially deleted, axonal segmentation was not lost proportionally with the amount of sclerotome removed, suggesting that properties that may vary with sclerotome volume (such as diffusible cues) do not play a primary role. Instead, spinal nerves lost segmentation only when ventral sclerotome was deleted, regardless of whether dorsal sclerotome was or was not removed. This strongly suggests that axonal segmentation is imposed by direct interactions between growth cones and extracellular matrices or surfaces sclerotome cells. While DRG tended to be normally segmented when ventral sclerotome was deleted and to lose segmentation when dorsomedial sclerotome was absent, a coordinate loss of DRG segmentation with sclerotome volume could not be ruled out. However it is clear that axonal and DRG segmentation are independent. Observations on a subset of embryos in which the notochord was displaced relative to the spinal cord suggest that the ventromedial sclerotome surrounding the notochord inhibits axon advance. Posterior and ventromedial sclerotome are hypothesized to act as barriers to axon outgrowth due to some feature of their common cartilaginous development. Specific innervation patterns were also examined. When the notochord was displaced toward the control limb, axons on this side made and corrected projection errors, suggesting that the notochord can influence the precision of axonal pathway selection. In contrast, motor axons that entered the limb on all operated sides innervated muscle with their normal precision despite the absence of the somite and axonal segmentation. Therefore, the somite and the process of spinal nerve segmentation are largely irrelevant to the specificity of motoneuron projection.
在部分或完全去除鸡胚体节中胚层后,研究了有模式的轴突生长和背根神经节(DRG)形成的发育情况。由于生皮节并非必需,且肢体肌肉能完全发育,因此神经模式的改变可归因于体节中硬骨节的缺失。当完全去除体节组织时,轴突会延伸且DRG会形成,但呈无节段模式。所以,体节并非引发轴突生长或DRG前体细胞迁移的必要条件,它不是必需的底物,也不是DRG凝聚所必需的。这些结果表明,后部硬骨节对轴突侵入具有相对抑制作用,当硬骨节缺失时这种抑制作用会解除。当部分去除体节时,轴突节段化并不会与去除的硬骨节数量成比例地丧失,这表明可能随硬骨节体积变化的特性(如可扩散信号)并非起主要作用。相反,只有当腹侧硬骨节被去除时,脊神经才会失去节段化,而无论背侧硬骨节是否被去除。这强烈表明,轴突节段化是由生长锥与细胞外基质或硬骨节细胞表面之间的直接相互作用所导致的。当腹侧硬骨节被去除时,DRG往往能正常节段化,而当背内侧硬骨节缺失时则会失去节段化,不过不能排除DRG节段化与硬骨节体积同步丧失的情况。然而,很明显轴突和DRG节段化是相互独立的。对一部分脊索相对于脊髓发生移位的胚胎的观察表明,围绕脊索的腹内侧硬骨节会抑制轴突前进。由于后部和腹内侧硬骨节在软骨发育方面有一些共同特征,因此推测它们会作为轴突生长的屏障。还研究了特定的神经支配模式。当脊索向对照肢体移位时,这一侧的轴突会产生并纠正投射错误,这表明脊索可影响轴突路径选择的精确性。相比之下,尽管没有体节和轴突节段化,但所有手术侧进入肢体的运动轴突仍能以正常的精确性支配肌肉。因此,体节和脊神经节段化过程在很大程度上与运动神经元投射的特异性无关。