Department of Pharmacy and BioTechnology, University of Bologna, Ex-BES Building, Via Selmi 3, Bologna, 40126, Italy.
Eur J Neurosci. 2014 Jan;39(2):176-85. doi: 10.1111/ejn.12407. Epub 2013 Nov 6.
CCAAT enhancer-binding protein β is a transcription factor that is involved in many brain processes, although its role in neuronal survival/death remains unclear. By using primary cultures of rat cerebellar granule neurons, we have shown here that CCAAT enhancer-binding protein β is present as all of its isoforms: the transcriptional activators liver activator proteins 1 and 2, and the transcriptional inhibitor liver inhibitory protein. We have also shown that liver activator protein 1 undergoes post-translational modifications, such as phosphorylation and sumoylation. These isoforms have different subcellular localizations, liver activator protein 2 being found in the cytosolic fraction only, liver inhibitory protein in the nucleus only, and liver activator protein 1 in both fractions. Through neuronal apoptosis induction by shifting mature cerebellar granule neurons to low-potassium medium, we have demonstrated that nuclear liver activator protein 1 expression decreases and its phosphorylation disappears, whereas liver inhibitory protein levels increase in the nuclear fraction, suggesting a pro-survival role for liver activator protein transcriptional activation and a pro-apoptotic role for liver inhibitory protein transcriptional inhibition. To confirm this, we transfected cerebellar granule neurons with plasmids expressing liver activator protein 1, liver activator protein 2, or liver inhibitory protein respectively, and observed that both liver activator proteins, which increase CCAAT-dependent transcription, but not liver inhibitory protein, counteracted apoptosis, thus demonstrating the pro-survival role of liver activator proteins. These data significantly improve our current understanding of the role of CCAAT enhancer-binding protein β in neuronal survival/apoptosis.
CCAAT 增强子结合蛋白 β 是一种参与许多大脑过程的转录因子,尽管其在神经元存活/死亡中的作用仍不清楚。通过使用大鼠小脑颗粒神经元的原代培养物,我们在这里表明 CCAAT 增强子结合蛋白 β 以其所有同工型存在:转录激活物肝激活蛋白 1 和 2 以及转录抑制剂肝抑制蛋白。我们还表明肝激活蛋白 1 经历翻译后修饰,如磷酸化和 sumoylation。这些同工型具有不同的亚细胞定位,肝激活蛋白 2 仅存在于细胞质部分,肝抑制蛋白仅存在于核内,肝激活蛋白 1 存在于这两个部分。通过将成熟的小脑颗粒神经元转移到低钾培养基中诱导神经元凋亡,我们证明核内肝激活蛋白 1 的表达减少,其磷酸化消失,而核内肝抑制蛋白水平增加,表明肝激活蛋白转录激活具有促生存作用,肝抑制蛋白转录抑制具有促凋亡作用。为了证实这一点,我们分别用表达肝激活蛋白 1、肝激活蛋白 2 或肝抑制蛋白的质粒转染小脑颗粒神经元,观察到增加 CCAAT 依赖性转录的两种肝激活蛋白(而不是肝抑制蛋白)可拮抗凋亡,从而证明肝激活蛋白具有促生存作用。这些数据显著提高了我们对 CCAAT 增强子结合蛋白 β 在神经元存活/凋亡中的作用的理解。