Alberta J A, Park S K, Mora J, Yuk D, Pawlitzky I, Iannarelli P, Vartanian T, Stiles C D, Rowitch D H
Department of Cancer Biology, Dana-Farber Cancer Institute and Harvard Medical School, 44 Binney Street, Boston, Massachusetts 02115, USA.
Mol Cell Neurosci. 2001 Oct;18(4):434-41. doi: 10.1006/mcne.2001.1026.
Oligodendrocyte precursor development in the embryonic spinal cord is thought to be regulated by the secreted signal, Sonic hedgehog (Shh). Such precursors can be identified by the expression of Olig genes, encoding basic helix-loop-helix factors, in the spinal cord and brain. However, the signaling pathways that govern oligodendrocyte precursor (OLP) development in the rostral central nervous system are poorly understood. Here, we show that Shh is required for oligodendrocyte development in the mouse forebrain and spinal cord, and that Shh proteins are both necessary and sufficient for OLP production in cortical neuroepithelial cultures. Moreover, adenovirus-mediated Olig1 ectopic expression can promote OLP formation independent of Shh activity. Our results demonstrate essential functions for Shh during early phases of oligodendrocyte development in the mammalian central nervous system. They further suggest that a key role of Shh signaling is activation of Olig genes.
胚胎脊髓中的少突胶质前体细胞发育被认为受分泌信号音猬因子(Shh)调控。此类前体细胞可通过脊髓和脑中编码碱性螺旋-环-螺旋因子的Olig基因的表达来识别。然而,对于调控前脑中枢神经系统中少突胶质前体细胞(OLP)发育的信号通路,我们了解甚少。在此,我们表明Shh是小鼠前脑和脊髓少突胶质细胞发育所必需的,并且Shh蛋白对于皮质神经上皮培养物中OLP的产生既是必需的也是充分的。此外,腺病毒介导的Olig1异位表达可独立于Shh活性促进OLP形成。我们的结果证明了Shh在哺乳动物中枢神经系统少突胶质细胞发育早期阶段的重要功能。它们进一步表明Shh信号传导的关键作用是激活Olig基因。