Merck Serono, Geneva 1202, Switzerland.
J Neurosci Res. 2010 Sep;88(12):2546-57. doi: 10.1002/jnr.22434.
Oligodendrocytes generate and maintain myelin, which is essential for axonal function and protection of the mammalian central nervous system. To advance our molecular understanding of differentiation by these cells, we screened libraries of pharmacologically active compounds and identified inducers of differentiation of Oli-neu, a stable cell line of mouse oligodendrocyte precursors (OPCs). We identified four broad classes of inducers, namely, forskolin/cAMP (protein kinase A activators), steroids (glucocorticoids and retinoic acid), ErbB2 inhibitors, and nucleoside analogs, and confirmed the activity of these compounds on rat primary oligodendrocyte precursors and mixed cortical cultures. We also analyzed transcriptional responses in the chemically induced mouse and rat OPC differentiation processes and compared these with earlier studies. We confirm the view that ErbB2 is a natural signaling component that is required for OPC proliferation, whereas ErbB2 inhibition or genetic knockdown results in OPC differentiation.
少突胶质细胞产生和维持髓鞘,这对轴突功能和保护哺乳动物中枢神经系统至关重要。为了深入了解这些细胞的分化,我们筛选了药物活性化合物文库,并鉴定出了诱导分化的物质,诱导物能诱导 Oli-neu(稳定的小鼠少突胶质前体细胞系)的分化。我们鉴定出了四大类诱导剂,即 forskolin/cAMP(蛋白激酶 A 激活剂)、类固醇(糖皮质激素和维甲酸)、ErbB2 抑制剂和核苷类似物,并证实了这些化合物对大鼠原代少突胶质前体细胞和混合皮质培养物的活性。我们还分析了化学诱导的小鼠和大鼠少突胶质前体细胞分化过程中的转录反应,并与早期的研究进行了比较。我们证实了 ErbB2 是一种天然的信号成分,它是少突胶质前体细胞增殖所必需的,而 ErbB2 抑制或基因敲低则导致少突胶质前体细胞分化。