Leblanc Scott E, Srinivasan Rajini, Ferri Cinzia, Mager Gennifer M, Gillian-Daniel Anne Lynn, Wrabetz Lawrence, Svaren John
Molecular and Cellular Pharmacology Training Program, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
J Neurochem. 2005 May;93(3):737-48. doi: 10.1111/j.1471-4159.2005.03056.x.
Myelination of peripheral nerves by Schwann cells requires a large amount of lipid and cholesterol biosynthesis. To understand the transcriptional coordination of the myelination process, we have investigated the developmental relationship between early growth response 2 (Egr2)/Krox20--a pivotal regulator of peripheral nerve myelination--and the sterol regulatory element binding protein (SREBP) pathway, which controls expression of cholesterol/lipid biosynthetic genes. During myelination of sciatic nerve, there is a very significant induction of SREBP1 and SREBP2, as well as their target genes, suggesting that the SREBP transactivators are important regulators in the myelination process. Egr2/Krox20 does not appear to directly regulate the levels of SREBP pathway components, but rather, we found that Egr2/Krox20 and SREBP transactivators can synergistically activate promoters of several SREBP target genes, indicating that direct induction of cholesterol/lipid biosynthetic genes by Egr2/Krox20 is a part of the myelination program regulated by this transactivator.
施万细胞对外周神经的髓鞘形成需要大量脂质和胆固醇的生物合成。为了解髓鞘形成过程中的转录协调,我们研究了早期生长反应2(Egr2)/Krox20(外周神经髓鞘形成的关键调节因子)与控制胆固醇/脂质生物合成基因表达的固醇调节元件结合蛋白(SREBP)途径之间的发育关系。在坐骨神经髓鞘形成过程中,SREBP1和SREBP2及其靶基因有非常显著的诱导,这表明SREBP反式激活因子是髓鞘形成过程中的重要调节因子。Egr2/Krox20似乎并不直接调节SREBP途径成分的水平,相反,我们发现Egr2/Krox20和SREBP反式激活因子可以协同激活几个SREBP靶基因的启动子,这表明Egr2/Krox20对胆固醇/脂质生物合成基因的直接诱导是由该反式激活因子调节的髓鞘形成程序的一部分。