Ninomiya T, Kobayashi E O
No To Shinkei. 1985 May;37(5):489-95.
Using the dorsal root ganglia (DRG), long-term cultures were done in neonatal (control) and senile (experimental) rats. The morphological analysis on myelin sheath formation was carried out by light microscopy, electron microscopy and image analyzing apparatus. The results are as follows: The neurites of senile DRG cells appeared 7 days later than the neurites of neonatal DRG cells. While the myelinations were observed in neonatal DRG culture by the third week, myelinations of senile DRG were also formed 7 days later. The myelin sheaths in both neonatal and senile DRG cultures looked much like those which were formed in vivo, but the number of myelinations in senile DRG culture was fewer than that of the neonatal DRG culture. In observations by electron microscopy, myelin lamellae numbered about 20 in both neonatal and senile DRG cultures with normal-appearing axon structures as seen in vivo. The discontinuities in the external lamina of Schwann cells were not observed in both the neonatal and senile DRG cultures. In the morphological analysis of neonatal and senile DRG cultures, the internodal length, diameter of myelin sheath and the length of nodal gap (distance between the rounded end of the compact myelin) were measured by image analyzing apparatus (MAGISCAN-I, Joyce Loebl LTD.) with Sudan black B stain. Although the internodal length of myelin sheath in senile DRG culture (144.9 +/- 40.7 microns) proved to be significantly longer than the neonatal DRG culture (131.6 +/- 26.2 microns) (p less than 0.01), the diameter of myelin sheath showed no significant difference between neonatal (2.9 +/- 0.7 micron) and senile (2.8 +/- 0.7 micron) DRG.(ABSTRACT TRUNCATED AT 250 WORDS)
利用背根神经节(DRG),在新生(对照)大鼠和老年(实验)大鼠中进行了长期培养。通过光学显微镜、电子显微镜和图像分析仪器对髓鞘形成进行了形态学分析。结果如下:老年DRG细胞的神经突比新生DRG细胞的神经突出现晚7天。虽然在新生DRG培养物中第三周观察到髓鞘形成,但老年DRG的髓鞘形成也在7天后出现。新生和老年DRG培养物中的髓鞘看起来与体内形成的髓鞘非常相似,但老年DRG培养物中的髓鞘形成数量少于新生DRG培养物。在电子显微镜观察中,新生和老年DRG培养物中的髓鞘板层数均约为20层,轴突结构外观正常,与体内所见相同。在新生和老年DRG培养物中均未观察到施万细胞外部板层的连续性中断。在新生和老年DRG培养物的形态学分析中,用图像分析仪器(MAGISCAN-I,乔伊斯·勒布尔有限公司)对苏丹黑B染色的髓鞘节间长度、髓鞘直径和结间隙长度(紧密髓鞘圆形末端之间的距离)进行了测量。尽管老年DRG培养物中髓鞘的节间长度(144.9±40.7微米)明显长于新生DRG培养物(131.6±26.2微米)(p<0.01),但新生(2.9±0.7微米)和老年(2.8±0.7微米)DRG的髓鞘直径无显著差异。(摘要截取自250字)