Vuorinen V, Siironen J, Röyttä M
Department of Neurosurgery, University Hospital of Helsinki, Finland.
Acta Neuropathol. 1995;89(3):209-18. doi: 10.1007/BF00309336.
In this study, we have analyzed the ability of axons to regenerate into chronically denervated peripheral nerve. As an experimental rat model, the proximal end of a newly transected rat tibial nerve was sutured into chronically denervated (3 months up to 16 months) common peroneal nerve. Samples for morphological studies were collected 3 and 6 weeks after anastomosis of the tibial and common peroneal nerves. Our results showing a distinct organization of the endoneurial matrix in the chronically denervated distal stumps conformed with those from previous studies. Long cytoplasmic processes of endoneurial fibroblasts in close contact with collagen fibrils (with a diameter of 50-60 nm) surrounded areas of thin collagen fibrils (with a diameter of 25-30 nm). Remnants of Schwann cell columns (i.e., bands of Büngner) were situated in areas of thin collagen fibrils. After 12 months of denervation the majority of the Schwann cells columns were replaced by thin collagen fibrils. Successful axonal regeneration was noted in distal stumps that had been denervated for 14 and even 16 months. However, axonal regeneration diminished with prolonged denervation. The regenerating axons grew through the areas of thin collagen fibrils. The maturation and thickening of the regenerated axonal sprouts resulted in a decrease in areas of thin collagen fibrils. These results suggest that a chronically denervated nerve stump has the capacity to meet regenerating axons even after 16 months of denervation, although the progressive atrophy of Schwann cell columns impairs the likelihood of good axonal regeneration. The areas of thin collagen fibrils may act as a 'plastic' bed for successful axonal regeneration, and a study of these fibrils may provide further insight into the role of the extracellular matrix during peripheral nerve regeneration.
在本研究中,我们分析了轴突向慢性失神经支配的周围神经再生的能力。作为实验大鼠模型,将新切断的大鼠胫神经近端缝合到慢性失神经支配(3个月至16个月)的腓总神经中。在胫神经和腓总神经吻合后3周和6周收集用于形态学研究的样本。我们的结果显示,慢性失神经支配的远端残端中神经内膜基质的独特组织与先前研究的结果一致。神经内膜成纤维细胞的长细胞质突起与胶原纤维(直径50 - 60纳米)紧密接触,围绕着细胶原纤维(直径25 - 30纳米)区域。雪旺细胞柱(即Büngner带)的残余物位于细胶原纤维区域。失神经支配12个月后,大多数雪旺细胞柱被细胶原纤维取代。在失神经支配14个月甚至16个月的远端残端中观察到了成功的轴突再生。然而,随着失神经支配时间延长,轴突再生减少。再生轴突穿过细胶原纤维区域。再生轴突芽的成熟和增粗导致细胶原纤维区域减少。这些结果表明,即使在失神经支配16个月后,慢性失神经支配的神经残端仍有能力迎接再生轴突,尽管雪旺细胞柱的逐渐萎缩损害了良好轴突再生的可能性。细胶原纤维区域可能作为轴突成功再生的“可塑性”床,对这些纤维的研究可能会进一步深入了解细胞外基质在周围神经再生过程中的作用。