Morrow D R, Campbell G, Lieberman A R, Anderson P N
Department of Anatomy and Developmental Biology, University College London, England.
Exp Neurol. 1993 Mar;120(1):60-9. doi: 10.1006/exnr.1993.1040.
Segments of peripheral nerve were autografted into the thalamus of adult rats. The peroneal nerve was used in one group, the tibial nerve (which has approximately twice the cross-sectional area of the peroneal nerve) in a second group, and two lengths of peroneal nerve side by side in a third group. Between 1 and 4 months later HRP was applied to the distal end of each graft to label neurons which had regenerated their axons into the graft. Serial coronal sections of each brain were reacted to reveal retrogradely transported HRP, and the positions of all labeled neurons were recorded in camera lucida drawings. In all three groups a few labeled neurons resembling thalamocortical projection cells were found in the dorsal thalamus close to the graft tip (mean number, 29 in the single peroneal group; 22 in the tibial group; and 14 in the double-peroneal group). However, neurons in the thalamic reticular nucleus (TRN) regenerated much more successfully into the larger nerve grafts; many more retrogradely labeled cells were found in animals with tibial or double-peroneal nerve grafts (mean number, 1.1 in the single-peroneal group; 272 in the tibial group; and 163 in the double-peroneal group). These neurons were concentrated in the sector of TRN known to project to the part of the dorsal thalamus containing the graft tip. The largest numbers of labeled neurons were found when the graft tip encroached upon the TRN. These results suggest that both graft size and graft position are critical determinants of the extent of axonal regeneration from the TRN. Larger grafts may be more copiously invaded by regenerating axons because such grafts damage larger numbers of TRN axons when implanted and/or because they stimulate regeneration by releasing critical quantities of neurotrophic factors.
将外周神经段自体移植到成年大鼠的丘脑。一组使用腓神经,第二组使用胫神经(其横截面积约为腓神经的两倍),第三组使用并排的两段腓神经。1至4个月后,将辣根过氧化物酶(HRP)应用于每个移植物的远端,以标记其轴突已再生进入移植物的神经元。对每个大脑的系列冠状切片进行反应,以显示逆行运输的HRP,并将所有标记神经元的位置记录在明视野绘图中。在所有三组中,在靠近移植物尖端的背侧丘脑中发现了一些类似于丘脑皮质投射细胞的标记神经元(单腓神经组平均数量为29个;胫神经组为22个;双腓神经组为14个)。然而,丘脑网状核(TRN)中的神经元向较大的神经移植物再生得更为成功;在接受胫神经或双腓神经移植物的动物中发现了更多逆行标记的细胞(单腓神经组平均数量为1.1个;胫神经组为272个;双腓神经组为163个)。这些神经元集中在TRN中已知投射到包含移植物尖端的背侧丘脑部分的区域。当移植物尖端侵入TRN时,发现的标记神经元数量最多。这些结果表明,移植物大小和移植物位置都是TRN轴突再生程度的关键决定因素。较大的移植物可能更容易被再生轴突侵入,因为这样的移植物在植入时会损伤更多数量的TRN轴突,和/或因为它们通过释放关键数量的神经营养因子来刺激再生。