Loughlin A J, Honegger P, Woodroofe M N, Comte V, Matthieu J M, Cuzner M L
Multiple Sclerosis Laboratory, Institute of Neurology, London, United Kingdom.
J Neurosci Res. 1994 Apr 1;37(5):647-53. doi: 10.1002/jnr.490370512.
The demyelinative potential of the cytokines interleukin-1 alpha (IL-1 alpha), interferon-gamma (IFN-gamma), and tumor necrosis factor-alpha (TNF-alpha) has been investigated in myelinating aggregate brain cell cultures. Treatment of myelinated cultures with these cytokines resulted in a reduction in myelin basic protein (MBP) content. This effect was additively increased by anti-myelin/oligodendrocyte glycoprotein (alpha-MOG) in the presence of complement. Qualitative immunocytochemistry demonstrated that peritoneal macrophages, added to the fetal telencephalon cell suspensions at the start of the culture period, successfully integrated into aggregate cultures. Supplementing the macrophage component of the cultures in this fashion resulted in increased accumulation of MBP. The effect of IFN-gamma on MBP content of cultures was not affected by the presence of macrophages in increased numbers.
白细胞介素-1α(IL-1α)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)这几种细胞因子的脱髓鞘潜能已在脑髓鞘化聚集细胞培养物中进行了研究。用这些细胞因子处理髓鞘化培养物会导致髓鞘碱性蛋白(MBP)含量降低。在补体存在的情况下,抗髓鞘/少突胶质细胞糖蛋白(α-MOG)会使这种效应累加增强。定性免疫细胞化学表明,在培养期开始时添加到胎儿端脑细胞悬液中的腹腔巨噬细胞成功整合到了聚集培养物中。以这种方式补充培养物中的巨噬细胞成分会导致MBP积累增加。培养物中巨噬细胞数量增加并不会影响IFN-γ对培养物MBP含量的作用。