Omlin F X, Webster H D, Palkovits C G, Cohen S R
J Cell Biol. 1982 Oct;95(1):242-8. doi: 10.1083/jcb.95.1.242.
To localize basic protein (BP) in the lamellar structure of central and peripheral myelin, we perfused newborn and 7-11-day rat pups with a phosphate-buffered fixative that contained 4% paraformaldehyde and 0.05 or 0.2% glutaraldehyde. Teased, longitudinally split or "brush" preparations of optic and trigeminal nerves were made by gently teasing apart groups of myelinated fibers with fine forceps or needles. Some of these preparations were immunostained without pretreatment in phosphate-buffered antiserum to BP according to the peroxidase-antiperoxidase method. Others were pretreated in ethanol before immunostaining. Then, all of them were dehydrated, embedded in Epon, and sectioned for electron microscopic study. In optic and trigeminal nerves that were not pretreated, myelin, glial cells, and their organelles were well preserved. BP immunostaining was present on cytoplasmic faces of oligodendroglial and Schwann cell membranes that formed mesaxons and loose myelin spirals. In compact central and peripheral myelin, reaction product was located in major dense line regions, and the myelin periodicity was the same as that observed in unstained control myelin that had been treated with preimmune serum. In ethanol-pretreated tissue, the myelin periodicity was reduced but dense line staining still was present. Our immunocytochemical demonstration of dense line localization of BP in both CNS and PNS myelin that was not disrupted or pretreated with solvents is important because of conflicting evidence in earlier immunostaining studies. Our results also support biochemical and histochemical evidence suggesting that BP exists in vivo as a membrane protein interacting with lipids on the cytoplasmic side of the bilayer in the spirally wrapped compact myelin membrane.
为了将碱性蛋白(BP)定位在中枢和外周髓鞘的板层结构中,我们用含有4%多聚甲醛和0.05%或0.2%戊二醛的磷酸盐缓冲固定剂灌注新生和7 - 11日龄的大鼠幼崽。通过用精细镊子或针轻轻分开成束的有髓纤维,制作了视神经和三叉神经的 teased、纵向劈开或“刷状”标本。其中一些标本按照过氧化物酶 - 抗过氧化物酶方法,在未用磷酸盐缓冲抗血清预处理的情况下对BP进行免疫染色。其他标本在免疫染色前用乙醇预处理。然后,将所有标本脱水,包埋在环氧树脂中,并切片进行电子显微镜研究。在未预处理的视神经和三叉神经中,髓鞘、神经胶质细胞及其细胞器保存良好。BP免疫染色出现在形成轴系膜和松散髓鞘螺旋的少突胶质细胞膜和施万细胞膜的胞质面上。在致密的中枢和外周髓鞘中,反应产物位于主要致密线区域,并且髓鞘周期性与用免疫前血清处理的未染色对照髓鞘中观察到的相同。在乙醇预处理的组织中,髓鞘周期性降低,但致密线染色仍然存在。我们对BP在中枢神经系统和外周神经系统髓鞘中的致密线定位进行的免疫细胞化学证明,即在未被破坏或用溶剂预处理的情况下,这一点很重要,因为早期免疫染色研究存在相互矛盾的证据。我们的结果还支持生物化学和组织化学证据,表明BP在体内作为一种膜蛋白存在,与螺旋包裹的致密髓鞘膜双层胞质侧的脂质相互作用。