Department of Biological Sciences, University of Ulsan, Ulsan 680-749, South Korea.
J Biol Chem. 2010 Aug 6;285(32):25074-84. doi: 10.1074/jbc.M110.100545. Epub 2010 Jun 10.
NELL2 (neural tissue-specific epidermal growth factor-like repeat domain-containing protein) is a secreted glycoprotein that is predominantly expressed in neural tissues. We reported previously that NELL2 mRNA abundance in brain is increased by estrogen (E2) treatment and that NELL2 is involved in the E2-dependent organization of a sexually dimorphic nucleus in the preoptic area. In this study we cloned the mouse NELL2 promoter and found it to contain two half-E2 response elements. Electrophoretic mobility shift assays and promoter assays showed that E2 and its receptors (ERalpha and ERbeta) stimulated NELL2 transcription by binding to the two half-E2 response elements. Hippocampal neuroprogenitor HiB5 cells expressing recombinant NELL2 showed increased cell survival under cell death-inducing conditions. Blockade of endogenous synthesis of NELL2 in HiB5 cells abolished the cell survival effect of E2 and resulted in a decrease in phosphorylation of extracellular signal-regulated kinase 1 and 2 (ERK1/2). These data suggest that the NELL2 gene is trans-activated by E2 and contributes to mediating the survival promoting effects of E2 via intracellular signaling pathway of ERK.
NELL2(神经组织特异性表皮生长因子样重复蛋白域包含蛋白)是一种分泌型糖蛋白,主要在神经组织中表达。我们之前报道过,雌激素(E2)处理会增加脑中 NELL2 mRNA 的丰度,并且 NELL2 参与了前脑区性别二态核的 E2 依赖性组织。在这项研究中,我们克隆了小鼠 NELL2 启动子,发现它包含两个半 E2 反应元件。电泳迁移率变动分析和启动子分析表明,E2 及其受体(ERalpha 和 ERbeta)通过与两个半 E2 反应元件结合,刺激 NELL2 转录。表达重组 NELL2 的海马神经前体细胞 HiB5 在诱导细胞死亡的条件下表现出细胞存活率增加。在 HiB5 细胞中阻断内源性 NELL2 的合成,消除了 E2 的细胞存活作用,并导致细胞外信号调节激酶 1 和 2(ERK1/2)的磷酸化减少。这些数据表明,E2 可使 NELL2 基因反式激活,并通过 ERK 的细胞内信号通路,促进 E2 发挥促进存活的作用。