Chau Wai Kei, So Kwok-Fai, Tay David, Dockery Peter
Department of Anatomy, The University of Hong Kong, Hong Kong, China.
Restor Neurol Neurosci. 2000;16(2):105-116.
In the present study we have morphometrically examined a regeneration model in which axons normally residing in CNS have regrown and are interacting with Schwann cells from the PNS. This study will not only provide morphometric data on regenerated optic fibers but also shed light on possible factors in determining the fiber morphometry. METHODS: The optic nerves of rats aged 6 weeks were cut intra-orbitally and replaced with a autologous sciatic nerve. After a survival period of 9 months, the graft or "regenerated" nerves containing the regenerated optic axons and Schwann cells were processed for morphometric measurements. RESULTS: The mean myelinated axon diameter of regenerated nerve (1.8 +/- 0.2 micro m) was significantly (P < 0.05) greater than that of the optic nerve (0.9 +/- 0.03 micro m). However, unmyelinated regenerated optic axons had a smaller mean axon diameter (0.49 +/- 0.04 micro m) than normal myelinated optic axons. This may suggest that myelinating glial cells exert an influence on axon caliber and Schwann cells seem to have greater effect than oligodendrocytes. The mean g-ratio showing the relative myelin sheath thickness was found to be the highest in the optic nerve (0.78 +/- 0.003), least in the sciatic nerve (0.6 +/- 0.009) and intermediate in the regenerated nerve (0.68 +/- 0.01). The results indicated that Schwann cells myelinating the regenerated optic axons have produced a thinner myelin sheath. Intra-axonally, no significant difference was detected in the number of axonal microtubules and neurofilaments between the regenerated and optic nerves. Therefore the disposition of microtubules and neurofilaments into axon may be intrinsically determined. CONCLUSIONS: In this study, we have identified some of the extrinsic and intrinsic factors in determining the fiber morphometry of the regen-erated nerve. The axon-size and myelination by glial cells were determined through the external axon-glial interactions, whereas the number of axonal microtubules and neurofilaments were intrinsically determined.
在本研究中,我们对一种再生模型进行了形态计量学研究,在该模型中,通常存在于中枢神经系统的轴突已经再生,并与来自周围神经系统的雪旺细胞相互作用。本研究不仅将提供再生视神经纤维的形态计量学数据,还将阐明决定纤维形态计量学的可能因素。方法:将6周龄大鼠的视神经在眶内切断,并用自体坐骨神经进行置换。在存活9个月后,对含有再生视神经轴突和雪旺细胞的移植物或“再生”神经进行形态计量学测量。结果:再生神经的有髓轴突平均直径(1.8±0.2μm)显著大于视神经(0.9±0.03μm)(P<0.05)。然而,无髓再生视神经轴突的平均轴突直径(0.49±0.04μm)比正常有髓视神经轴突小。这可能表明,形成髓鞘的神经胶质细胞对轴突管径有影响,且雪旺细胞的作用似乎比少突胶质细胞更大。显示相对髓鞘厚度的平均g比值在视神经中最高(0.78±0.003),在坐骨神经中最低(0.6±0.009),在再生神经中居中(0.68±0.01)。结果表明,为再生视神经轴突形成髓鞘的雪旺细胞产生的髓鞘较薄。在轴突内,再生神经和视神经之间的轴突微管和神经丝数量未检测到显著差异。因此,微管和神经丝在轴突中的分布可能是由内在因素决定的。结论:在本研究中,我们确定了一些决定再生神经纤维形态计量学的外在和内在因素。轴突大小和神经胶质细胞的髓鞘形成是通过轴突与神经胶质细胞的外部相互作用决定的,而轴突微管和神经丝的数量是由内在因素决定的。