Milner R, Anderson H J, Rippon R F, McKay J S, Franklin R J, Marchionni M A, Reynolds R, Ffrench-Constant C
Wellcome/CRC Institute of Developmental Biology and Cancer, Cambridge, England.
Glia. 1997 Jan;19(1):85-90. doi: 10.1002/(sici)1098-1136(199701)19:1<85::aid-glia9>3.0.co;2-9.
We have examined the effects of the mitogenic growth factors platelet derived growth factor (PDGF), basic fibroblast growth factor (bFGF) and glial growth factor-2 (GGF-2) on oligodendrocyte precursor migration. In an agarose drop migration assay PDGF and bFGF stimulated migration while GGF-2 had no effect. The migration-enhancing effect of bFGF cannot be blocked by neutralising antibodies against PDGF, confirming that this effect is direct and not mediated via upregulation of PDGF receptors. Based on our results, we propose a model in which the differing effects of PDGF and GGF-2 ensure appropriate numbers of oligodendrocyte precursor cells in the vicinity of axons to be myelinated during development.
我们研究了促有丝分裂生长因子血小板衍生生长因子(PDGF)、碱性成纤维细胞生长因子(bFGF)和神经胶质生长因子-2(GGF-2)对少突胶质细胞前体迁移的影响。在琼脂糖滴迁移试验中,PDGF和bFGF刺激迁移,而GGF-2没有作用。bFGF的迁移增强作用不能被抗PDGF的中和抗体阻断,这证实了这种作用是直接的,而非通过上调PDGF受体介导。基于我们的结果,我们提出了一个模型,其中PDGF和GGF-2的不同作用确保了在发育过程中,轴突附近有适当数量的少突胶质细胞前体细胞用于髓鞘形成。