Cellular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037, USA.
J Biol Chem. 2010 Dec 10;285(50):38915-22. doi: 10.1074/jbc.M110.170274. Epub 2010 Sep 28.
Glial fibrillary acidic protein (GFAP) is the main astroglial marker during astrogliogenesis, but it is also expressed in other cell types, including neural stem cells and old neurons. Activation of the JAK/STAT pathway by the IL-6 family of cytokines is the canonical pathway regulating GFAP expression, whereas retinoic acid is thought to be the only inducer of GFAP to operate independently of this pathway. Here, we show that retinoic acid receptor α not only links retinoic acid signaling to the canonical cytokine-stimulated pathway leading to GFAP expression but that it also plays a key role in the synergistic actions of retinoic acid and cytokines on this pathway. Cytokines both potentiate retinoic acid receptor α expression and enhance its binding to DNA and to the Stat3-p300/CBP-Smad transcriptional complex, the cornerstone of the canonical pathway. PI3K is upstream to all the key events leading to the expression of GFAP. Our results give new insights about the role of retinoic acid signaling in GFAP expression.
胶质纤维酸性蛋白(GFAP)是星形胶质细胞发生过程中的主要星形胶质细胞标志物,但它也在其他细胞类型中表达,包括神经干细胞和衰老神经元。白细胞介素-6 家族细胞因子激活 JAK/STAT 途径是调节 GFAP 表达的经典途径,而视黄酸被认为是唯一独立于该途径诱导 GFAP 的诱导剂。在这里,我们表明视黄酸受体 α 不仅将视黄酸信号与导致 GFAP 表达的经典细胞因子刺激途径联系起来,而且在视黄酸和细胞因子对该途径的协同作用中发挥关键作用。细胞因子既增强视黄酸受体 α 的表达,又增强其与 DNA 的结合以及 Stat3-p300/CBP-Smad 转录复合物的结合,这是经典途径的基石。PI3K 是导致 GFAP 表达的所有关键事件的上游。我们的结果为视黄酸信号在 GFAP 表达中的作用提供了新的见解。