Dahm L M, Landmesser L T
University of Connecticut, Department of Physiology and Neurobiology, Storrs 06268.
Dev Biol. 1988 Dec;130(2):621-44. doi: 10.1016/0012-1606(88)90357-0.
In vertebrates, approximately 50% of the lumbosacral motoneurons die during a short period of development that coincides with synaptogenesis in the limb. Although it has been postulated that these motoneurons die because they fail to obtain adequate trophic support from the muscles, it is not clear how this factor is supplied. The mechanism by which activity blockade prevents motoneurons cell death is also unknown. In order to begin to understand the nature of these proposed trophic interactions, we have examined the temporal sequence of axonal invasion and ramification within two muscles of the chick hindlimb, the predominantly slow iliofibularis and the fast posterior iliotibialis, during the cell death period. We found striking differences in intramuscular nerve ingrowth and branching between fast and slow muscle. We also observed differences in the molecular composition of fast and slow myotubes that may contribute to the nerve pattern differences. In addition, we observed a progressive increase in the degree of intramuscular nerve fasciculation as well as a precise temporal sequence of nerve branching. The earliest detectable response to chronic curarization was a dramatic decrease in the degree of intramuscular nerve fasciculation. Activity blockade also greatly enhanced nerve branching within the muscles from the time that nerve branches normally formed, and, additionally, interfered with the normal cessation of axon growth. Our results support the idea that nerve endings are the sites of trophic uptake. Furthermore, although our results do not allow us to exclude other activity-dependent influences on motoneuron survival, they suggest the following testable hypotheses: (1) the normal regulation of motoneuron survival may result from the precise control of intramuscular nerve branching, (2) activity blockade may increase motoneuron survival by enhancing intramuscular nerve branching, and (3) anything which affects this complex process of nerve branching may also alter motoneuron survival.
在脊椎动物中,约50%的腰骶部运动神经元在与肢体突触形成同步的短发育时期内死亡。尽管有人推测这些运动神经元死亡是因为它们未能从肌肉获得足够的营养支持,但尚不清楚这种营养因子是如何供应的。活动阻断防止运动神经元细胞死亡的机制也不清楚。为了开始理解这些假定的营养相互作用的本质,我们研究了在细胞死亡期间,鸡后肢两块肌肉(主要是慢肌髂胫束肌和快肌后髂胫肌)内轴突侵入和分支的时间顺序。我们发现快肌和慢肌在肌内神经长入和分支方面存在显著差异。我们还观察到快肌和慢肌肌管的分子组成存在差异,这可能导致神经模式的差异。此外,我们观察到肌内神经束的程度逐渐增加以及神经分支有精确的时间顺序。对慢性箭毒化最早可检测到的反应是肌内神经束程度的显著降低。活动阻断还从神经分支正常形成之时起极大地增强了肌肉内的神经分支,此外,还干扰了轴突生长的正常停止。我们的结果支持神经末梢是营养摄取部位的观点。此外,尽管我们的结果不允许我们排除其他对运动神经元存活的活动依赖性影响,但它们提出了以下可检验的假设:(1)运动神经元存活的正常调节可能源于对肌内神经分支的精确控制,(2)活动阻断可能通过增强肌内神经分支来增加运动神经元存活,(3)任何影响神经分支这一复杂过程的因素也可能改变运动神经元存活。