Lemke G, Chao M
Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, San Diego, CA 92138.
Development. 1988 Mar;102(3):499-504. doi: 10.1242/dev.102.3.499.
The elaboration of myelin by Schwann cells is triggered by contact with appropriate peripheral axons. Among the most prominent features of this interaction is the activation and high-level expression of the genes encoding the major myelin proteins P0 and Myelin Basic Protein (MBP). Although the initial induction of these genes is thought to be dependent upon contact with axons, neither the inductive signal of the axon nor the receptor and associated second messenger system of the Schwann cell that transduces this signal has been identified. In this report, we demonstrate that expression of the P0 and MBP genes in rapidly myelinating Schwann cells is sharply reduced upon withdrawal of axons, but that this expression can be substantially restored by agents that raise the intracellular concentration of cyclic AMP. We further show that Schwann cell expression of a third gene, i.e. that encoding the Nerve Growth Factor receptor, is strongly activated by the withdrawal of axons, and that this activation is largely independent of cAMP.
施万细胞形成髓鞘的过程是由与合适的外周轴突接触所触发的。这种相互作用最显著的特征之一是编码主要髓鞘蛋白P0和髓鞘碱性蛋白(MBP)的基因被激活并高水平表达。尽管这些基因的初始诱导被认为依赖于与轴突的接触,但轴突的诱导信号以及转导该信号的施万细胞受体和相关第二信使系统均未被确定。在本报告中,我们证明,在轴突撤离后,快速形成髓鞘的施万细胞中P0和MBP基因的表达会急剧下降,但通过提高细胞内环磷酸腺苷(cAMP)浓度的试剂可使这种表达得到显著恢复。我们进一步表明,第三个基因(即编码神经生长因子受体的基因)在施万细胞中的表达会因轴突撤离而被强烈激活,并且这种激活在很大程度上不依赖于cAMP。