Kamaraju Anil K, Adjalley Sophie, Zhang Peilin, Chebath Judith, Revel Michel
Department of Molecular Genetics, Weizmann Institute of Science, Rehov Herzl, Rehovot 76100, Israel.
J Biol Chem. 2004 Jan 30;279(5):3852-61. doi: 10.1074/jbc.M310443200. Epub 2003 Nov 3.
Expression of genes encoding structural myelin proteins marks the inception of the myelinating Schwann cell (SC) phenotype. Earlier embryonic SC as well as adult non-myelinating SC produce the intermediate filament glial fibrillary acid protein (GFAP), which disappears from the myelinating SC. We previously observed that triggering of the gp130 receptor system by the IL6RIL6 ligand, comprising interleukin-6 (IL-6) fused to the soluble IL-6 receptor, induces myelin gene expression in rat embryonic dorsal root ganglia (DRG) cultures as well as in the murine melanoma cell line B16/F10.9. Study of target genes regulated by IL6RIL6 indicates a strong and selective induction of the transcriptional regulator C/EBP-delta in DRG cultures and in the F10.9 cell line. As shown here, silencing of C/EBP-delta mRNA and protein expression by introduction of small interference RNA-producing plasmids in the F10.9 cells prevented the induction of myelin protein zero (P0) and myelin basic protein (MBP) mRNAs by IL6RIL6. Doxycycline-regulated overexpression of C/EBP-delta was sufficient to induce accumulation of P0 and MBP mRNAs, the effect being selective, because C/EBP-delta did not affect several other genes strongly regulated by IL6RIL6. Interestingly, GFAP was inhibited by C/EBP-delta overexpression, leading to a modulation of the ratio between myelin gene products versus GFAP and suggesting that C/EBP-delta plays a role in the switch to a myelinating phenotype. The down-regulation of Pax3, also typical of the transition to myelinating cells, was observed after C/EBP-delta expression in correlation to P0 induction and to decrease of melanogenesis and cell growth. In cultures of dissociated cells of embryonic rat DRG, where we knocked-down the C/EBP-delta mRNA, we found an inhibition of P0 mRNA induction by IL6RIL6, showing that the role of C/EBP-delta on this myelin gene is not unique to the melanoma system.
编码结构性髓鞘蛋白的基因表达标志着髓鞘形成雪旺细胞(SC)表型的起始。早期胚胎期的SC以及成年非髓鞘形成的SC会产生中间丝胶质纤维酸性蛋白(GFAP),而该蛋白在髓鞘形成的SC中消失。我们之前观察到,由IL6RIL6配体(包含与可溶性IL-6受体融合的白细胞介素-6(IL-6))触发gp130受体系统,可诱导大鼠胚胎背根神经节(DRG)培养物以及小鼠黑色素瘤细胞系B16/F10.9中的髓鞘基因表达。对受IL6RIL6调控的靶基因的研究表明,在DRG培养物和F10.9细胞系中,转录调节因子C/EBP-δ受到强烈且选择性的诱导。如此处所示,通过在F10.9细胞中引入产生小干扰RNA的质粒来沉默C/EBP-δ mRNA和蛋白表达,可阻止IL6RIL6对髓鞘蛋白零(P0)和髓鞘碱性蛋白(MBP)mRNA的诱导。强力霉素调节的C/EBP-δ过表达足以诱导P0和MBP mRNA的积累,这种效应具有选择性,因为C/EBP-δ并未影响其他几个受IL6RIL6强烈调控的基因。有趣的是,C/EBP-δ过表达会抑制GFAP,导致髓鞘基因产物与GFAP之间的比例发生调节,这表明C/EBP-δ在向髓鞘形成表型的转变中发挥作用。在C/EBP-δ表达后,观察到Pax3的下调,这也是向髓鞘形成细胞转变的典型特征,与P0诱导以及黑色素生成和细胞生长的减少相关。在胚胎大鼠DRG的解离细胞培养物中,我们敲低了C/EBP-δ mRNA,发现IL6RIL6对P0 mRNA的诱导受到抑制,这表明C/EBP-δ对该髓鞘基因的作用并非黑色素瘤系统所特有。