Le Beau J M, Ellisman M H, Powell H C
Department of Pathology, University of California, San Diego, La Jolla.
J Neurocytol. 1988 Apr;17(2):161-72. doi: 10.1007/BF01674203.
Light and electron microscopy were used to investigate long-term regeneration in peripheral nerves regenerating across a 10 mm gap through silicone tubes. Schwann cells and axons co-migrated behind an advancing front of fibroblasts, bridging the 10 mm gap between 28 and 35 days following nerve transection. Myelination of regenerated fibres started between 14 and 21 days after transection and occurred in a manner similar to that reported during development. Although these early events were successful in producing morphologically normal-appearing regenerated fibres, complete maturation of many of these fibres was never achieved. Axonal distortion by neurofilaments, axonal degeneration and secondary demyelination were seen at 56 days following nerve transection. These changes progressed in severity with time as more axons advanced through the distal stump towards their peripheral target. Since regeneration occurs in the absence of endoneurial tubes, and because constrictive forces act on the nerve during regeneration, we suggest that these extrinsic factors limit the successful advancement of axons through the distal stump to their target organ.
利用光学显微镜和电子显微镜研究了周围神经通过硅胶管跨越10毫米间隙的长期再生情况。雪旺细胞和轴突在成纤维细胞前进前沿之后共同迁移,在神经横断后28至35天之间桥接了10毫米的间隙。再生纤维的髓鞘形成在横断后14至21天开始,其发生方式与发育过程中报道的相似。尽管这些早期事件成功地产生了形态上看似正常的再生纤维,但许多这些纤维从未完全成熟。在神经横断后56天可见神经丝引起的轴突扭曲、轴突变性和继发性脱髓鞘。随着更多轴突通过远端残端向其外周靶标推进,这些变化的严重程度随时间进展。由于再生在没有神经内膜管的情况下发生,并且由于在再生过程中收缩力作用于神经,我们认为这些外在因素限制了轴突通过远端残端成功推进到其靶器官。