Brammer M J, Carey S G
J Neurochem. 1980 Oct;35(4):873-9. doi: 10.1111/j.1471-4159.1980.tb07085.x.
Oligodendrocyte perikarya have been prepared from fresh and frozen bovine corpus callosum by a slight modification of previously published methods. The properties of the cells which we have obtained appear to be very similar to those previously described in other laboratories. Oligodendrocyte homogenates have been incubated with radioactive choline and inositol in the presence of a number of possible cofactors of phospholipid synthesis. Choline was incorporated into oligodendrocyte phosphatidylcholine both by synthesis de novo and by Ca2+-stimulated base exchange. There was no detectable incorporation of choline into sphingomyelin by either of these routes. Inositol was incorporated into oligodendrocyte phosphatidylinositol by synthesis de novo and by Mn2+-stimulated exchange. Oligodendrocyte homogenates were found to contain sufficient endogenous Ca2+ both to stimulate significant incorporation of choline into lecithin by base exchange and to produce considerable inhibition of lecithin synthesis de novo.
少突胶质细胞胞体是通过对先前发表的方法稍作修改,从新鲜和冷冻的牛胼胝体中制备出来的。我们所获得的细胞特性似乎与其他实验室先前描述的非常相似。少突胶质细胞匀浆已在多种可能的磷脂合成辅助因子存在的情况下,与放射性胆碱和肌醇一起孵育。胆碱通过从头合成和Ca2+刺激的碱基交换掺入少突胶质细胞磷脂酰胆碱中。通过这两种途径,均未检测到胆碱掺入鞘磷脂中。肌醇通过从头合成和Mn2+刺激的交换掺入少突胶质细胞磷脂酰肌醇中。发现少突胶质细胞匀浆含有足够的内源性Ca2+,既能通过碱基交换刺激胆碱大量掺入卵磷脂中,又能对卵磷脂的从头合成产生相当大的抑制作用。