Department of Pharmacology, University of Cambridge, Cambridge, UK.
J Neurochem. 2010 Feb;112(4):1065-73. doi: 10.1111/j.1471-4159.2009.06521.x. Epub 2009 Dec 3.
Expression of the nuclear orphan receptor gene Nur77 in neuronal cells is induced by activity-dependent increases in intracellular Ca2+ ions. Ca2+ responsiveness of the Nur77 gene has been attributed to two distinct DNA regulatory regions that recruit the transcription factors cAMP response element binding protein (CREB) and myocyte enhancer factor-2 (MEF2). Here we used dominant interfering and constitutively active mutants of CREB and MEF2 proteins to assess their relative contribution to depolarization-induced Nur77 expression in undifferentiated PC12 cells and hippocampal neurons. We show that while CREB is necessary for Ca2+-activated Nur77 expression MEF2 functions to modulate CREB-dependent Nur77 expression by acting as a repressor in quiescent cells.
核孤儿受体基因 Nur77 在神经元细胞中的表达是由细胞内钙离子浓度的活性依赖性增加所诱导的。Nur77 基因的钙反应性归因于两个不同的 DNA 调节区域,它们募集转录因子 cAMP 反应元件结合蛋白 (CREB) 和肌细胞增强因子-2 (MEF2)。在这里,我们使用 CREB 和 MEF2 蛋白的显性干扰和组成性激活突变体来评估它们对未分化 PC12 细胞和海马神经元中去极化诱导的 Nur77 表达的相对贡献。我们表明,虽然 CREB 对于 Ca2+-激活的 Nur77 表达是必需的,但 MEF2 通过在静止细胞中作为抑制剂起作用来调节 CREB 依赖性 Nur77 表达。