Sikora E, Grassilli E, Radziszewska E, Bellesia E, Barbieri D, Franceschi C
Institute of General Pathology, University of Modena, Italy.
Biochem Biophys Res Commun. 1993 Dec 15;197(2):709-15. doi: 10.1006/bbrc.1993.2537.
The onset of apoptosis is generally thought to require the induction of a novel genetic program. Accordingly, we studied the kinetic of DNA-binding activity of several transcription factors in rat thymocytes undergoing apoptosis induced by dexamethasone (DEX) or heat shock (HS) treatment. Here we report that: 1) early activation of AP-1 occurred in both models of apoptosis, even if the intensity of activation and AP-1 complex composition were different and much less evident in HS-treated thymocytes; 2) early NFkB DNA-binding activity was also observed in both types of apoptosis; 3) downregulation of other transcription factors, such as OCT-1 and CREB, with high constitutive activity, was recorded in both models of apoptosis. The fact that some TFs are up-regulated while others are down-regulated suggests that apoptosis is the result of a complex combination of positive and negative signals regulating gene expression.
细胞凋亡的发生通常被认为需要诱导一种新的基因程序。因此,我们研究了几种转录因子在经地塞米松(DEX)或热休克(HS)处理诱导凋亡的大鼠胸腺细胞中的DNA结合活性动力学。在此我们报告:1)在两种细胞凋亡模型中均出现了AP-1的早期激活,即使激活强度和AP-1复合物组成有所不同,且在HS处理的胸腺细胞中不太明显;2)在两种类型的细胞凋亡中也均观察到早期NFkB DNA结合活性;3)在两种细胞凋亡模型中均记录到其他具有高组成活性的转录因子,如OCT-1和CREB的下调。一些转录因子上调而另一些转录因子下调这一事实表明,细胞凋亡是调节基因表达的正负信号复杂组合的结果。