Wang X M, Qin Y Q, Terman J R, Martin G F
Department of Cell Biology, Neurobiology and Anatomy, Ohio State University, College of Medicine, Columbus 43210, USA.
Brain Res Dev Brain Res. 1997 Feb 20;98(2):151-63. doi: 10.1016/s0165-3806(96)00167-8.
The first objective of the present study was to ask when axons of the fasciculus gracilis reach the nucleus gracilis in the North American opossum (Didelphis virginiana). When Fast Blue (FB) was injected into the lumbar cord on postnatal day (PD) 1 and the pups were killed 2 days later, labeled axons were present within a distinct fasciculus gracilis at thoracic and cervical levels of the cord. When comparable injections were made at PD3 or 5 and the pups were allowed to survive for the same time period, a few labeled axons could be followed to the caudal medulla where they were located dorsal to the presumptive nucleus gracilis. In order to verify these observations and to determine if any of the axons which innervate the nucleus gracilis early in development originate within dorsal root ganglia, we also employed cholera toxin conjugated to horseradish peroxidase (CT-HRP) to label dorsal root axons transganglionically. When CT-HRP was injected into the hindlimb on PD1 and the pups were maintained for 1 day prior to death and HRP histochemistry, labeled axons were present within the fasciculus gracilis at thoracic and cervical levels, but they could not be traced into the medulla. When comparable injections were made on PD3, and the pups were maintained for 2 days, labeled axons were present within the caudal medulla. Our second objective was to determine whether axons of the fasciculus gracilis grow through a lesion of their spinal pathway during early development. In one group of animals, the thoracic cord was transected at PD5, 8, 12, 20 and 26 and bilateral injections of Fast Blue (FB) were made four segments caudal to the lesion 30-40 days later. After a 3-5 day survival, the pups were killed and perfused so that the spinal cord and brainstem could be removed and sectioned for fluorescence microscopy. In all of the cases lesioned at PD5, axons of the fasciculus gracilis were labeled rostral to the site of transection and they could be followed to the nucleus gracilis. Evidence for growth of fasciculus gracilis axons into the caudal medulla was also seen in cases lesioned at PD8. In contrast, labeled axons were not observed rostral to the lesion when it was made at PD12 or at later stages of development. In order to verify that some of the axons which crossed the lesion originated within dorsal root ganglia, the thoracic cord was transected at PD5 in another group of animals and 7 days later, injections of CT-HRP were made into one of the hindlimbs. After a 3 day survival, labeled axons could be traced through the lesion site and into the caudal medulla. We conclude that axons of the fasciculus gracilis reach the nucleus gracilis by at least PD5 in the opossum and that they grow through a lesion of their spinal pathway when it is made at the same age or shortly thereafter. The critical period for such growth appears to end between PD8 and PD12.
本研究的首要目标是确定北美负鼠(弗吉尼亚负鼠)薄束的轴突何时到达薄束核。出生后第1天(PD1)将快蓝(FB)注入腰髓,2天后处死幼崽,在胸段和颈段脊髓的一个明显的薄束内发现了标记轴突。在PD3或PD5进行类似注射,并让幼崽存活相同时间,可追踪到一些标记轴突到达延髓尾部,它们位于假定薄束核的背侧。为了验证这些观察结果,并确定在发育早期支配薄束核的轴突是否有任何起源于背根神经节,我们还使用了与辣根过氧化物酶结合的霍乱毒素(CT-HRP)经神经节标记背根轴突。在PD1将CT-HRP注入后肢,在处死和进行HRP组织化学分析前将幼崽饲养1天,在胸段和颈段脊髓的薄束内发现了标记轴突,但无法追踪到延髓。在PD3进行类似注射,并将幼崽饲养2天,在延髓尾部发现了标记轴突。我们的第二个目标是确定薄束的轴突在早期发育过程中是否能穿过其脊髓通路的损伤部位。在一组动物中,在PD5、8、12、20和26切断胸段脊髓,30 - 40天后在损伤部位尾侧四个节段进行双侧快蓝(FB)注射。存活3 - 5天后,处死幼崽并进行灌注,以便取出脊髓和脑干并切片进行荧光显微镜检查。在所有PD5损伤的病例中,薄束的轴突在横断部位头侧被标记,并且可以追踪到薄束核。在PD8损伤的病例中也发现了薄束轴突向延髓尾部生长的证据。相反,在PD12或更晚发育阶段进行损伤时,在损伤部位头侧未观察到标记轴突。为了验证一些穿过损伤部位的轴突起源于背根神经节,在另一组动物的PD5切断胸段脊髓,7天后将CT-HRP注入一侧后肢。存活3天后,标记轴突可穿过损伤部位并追踪到延髓尾部。我们得出结论,在负鼠中,薄束的轴突至少在PD5时到达薄束核,并且当在相同年龄或此后不久造成脊髓通路损伤时,它们能穿过该损伤部位。这种生长的关键期似乎在PD8和PD12之间结束。