Politis M J, Spencer P S
J Neurocytol. 1981 Apr;10(2):221-32. doi: 10.1007/BF01257968.
This paper describes a surgical method of manipulating feline peripheral nerve regeneration to separate spatially the temporal sequence of events of axon-Schwann cell interaction during nerve fibre formation. The method allows regenerating axons from the peroneal nerve to reinnervate the distal stump of a axon- and myelin-free, Schwann cell-enriched, chronically denervated tibial nerve distal stump. Three zones can be morphologically delineated in the tibial nerve stump after three weeks of reinnervation: (1) a proximal myelinated zone, (2) a more distal, non-myelinated, axon-Schwann cell contact zone, and (3) a distal axon-free Schwann cell non-contact zone. The distal limit of the second zone can be determined accurately by the front of an axonally transported label. The large volume of available tissue makes this method suitable for interdisciplinary studies to elucidate the control of axon elongation, axon growth, and axon-Schwann cell inter-relationships.
本文描述了一种手术方法,用于操控猫的外周神经再生,以便在神经纤维形成过程中在空间上分离轴突与施万细胞相互作用的时间顺序。该方法能使来自腓神经的再生轴突重新支配一个无轴突和髓鞘、富含施万细胞且长期去神经支配的胫神经远端残端的远端残端。再支配三周后,在胫神经残端可在形态上划分出三个区域:(1)近端有髓鞘区域,(2)更远端的无髓鞘轴突 - 施万细胞接触区域,以及(3)远端无轴突的施万细胞非接触区域。第二个区域的远端界限可通过轴突运输标记的前沿精确确定。大量可用组织使得该方法适用于跨学科研究,以阐明轴突伸长、轴突生长以及轴突与施万细胞相互关系的控制机制。