Miao N, Wang M, Ott J A, D'Alessandro J S, Woolf T M, Bumcrot D A, Mahanthappa N K, Pang K
Ontogeny, Inc., Cambridge, Massachusetts 02138, USA.
J Neurosci. 1997 Aug 1;17(15):5891-9. doi: 10.1523/JNEUROSCI.17-15-05891.1997.
Sonic hedgehog (Shh), an axis-determining secreted protein, is expressed during early vertebrate embryogenesis in the notochord and ventral neural tube. In this site it plays a role in the phenotypic specification of ventral neurons along the length of the CNS. For example, Shh induces the differentiation of motor neurons in the spinal cord and dopaminergic neurons in the midbrain. Shh expression, however, persists beyond this induction period, and we have asked whether the protein shows novel activities beyond phenotype specification. Using cultures derived from embryonic day 14.5 (E14. 5) rat ventral mesencephalon, we show that Shh is also trophic for dopaminergic neurons. Interestingly, Shh not only promotes dopaminergic neuron survival, but also promotes the survival of midbrain GABA-immunoreactive (GABA-ir) neurons. In cultures derived from the E15-16 striatum, Shh promotes the survival of GABA-ir interneurons to the exclusion of any other cell type. Cultures derived from E15-16 ventral spinal cord reveal that Shh is again trophic for interneurons, many of which are GABA-ir and some of which express the Lim-1/2 nuclear marker, but it does not appear to support motorneuron survival. Shh does not support the survival of sympathetic or dorsal root ganglion neurons. Finally, using the midbrain cultures, we show that in the presence of MPP+, a highly specific neurotoxin, Shh prevents dopaminergic neuron death that normally would have occurred. Thus Shh may have therapeutic value as a protective agent in neurodegenerative disease.
音猬因子(Shh)是一种决定轴的分泌蛋白,在脊椎动物胚胎发育早期的脊索和腹侧神经管中表达。在这个部位,它在中枢神经系统全长腹侧神经元的表型特化中发挥作用。例如,Shh诱导脊髓中运动神经元和中脑中多巴胺能神经元的分化。然而,Shh的表达在这个诱导期之后仍然持续,我们不禁要问,该蛋白是否具有超越表型特化的新活性。利用来自胚胎第14.5天(E14.5)大鼠腹侧中脑的培养物,我们发现Shh对多巴胺能神经元也具有营养作用。有趣的是,Shh不仅能促进多巴胺能神经元的存活,还能促进中脑γ-氨基丁酸免疫反应性(GABA-ir)神经元的存活。在来自E15 - 16纹状体的培养物中,Shh促进GABA-ir中间神经元的存活,而排除任何其他细胞类型。来自E15 - 16腹侧脊髓的培养物显示,Shh对中间神经元同样具有营养作用,其中许多是GABA-ir神经元,有些还表达Lim-1/2核标记,但它似乎不支持运动神经元的存活。Shh不支持交感神经或背根神经节神经元的存活。最后,利用中脑培养物,我们发现,在存在高度特异性神经毒素MPP⁺的情况下,Shh可防止通常会发生的多巴胺能神经元死亡。因此,Shh作为神经退行性疾病的一种保护剂可能具有治疗价值。