Ulfhammer Erik, Larsson Pia, Magnusson Mia, Karlsson Lena, Bergh Niklas, Jern Sverker
The Wallenberg Laboratory for Cardiovascular Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, 413 45 Gothenburg, Sweden.
Int J Vasc Med. 2016;2016:7928681. doi: 10.1155/2016/7928681. Epub 2016 Feb 7.
Objective. Endothelial tissue-type plasminogen activator (t-PA) release is a pivotal response to protect the circulation from occluding thrombosis. We have shown that the t-PA gene is epigenetically regulated and greatly induced by the histone deacetylase (HDAC) inhibitor valproic acid (VPA). We now investigated involvement of known t-PA promoter regulatory elements and evaluated dependence of potential interacting transcription factors/cofactors. Methods. A reporter vector with an insert, separately mutated at either the t-PA promoter CRE or GC box II or GC box III elements, was transfected into HT-1080 and HUVECs and challenged with VPA. HUVECs were targeted with siRNA against histone acetyl transferases (HAT) and selected transcription factors from the Sp/KLF family. Results. An intact VPA-response was observed with CRE mutated constructs, whereas mutation of GC boxes II and III reduced the magnitude of the induction by 54 and 79% in HT-1080 and 49 and 50% in HUVECs, respectively. An attenuated induction of t-PA mRNA was observed after Sp2, Sp4, and KLF5 depletion. KLF2 and p300 (HAT) were identified as positive regulators of basal t-PA expression and Sp4 and KLF9 as repressors. Conclusion. VPA-induced t-PA expression is dependent on the proximal GC boxes in the t-PA promoter and may involve interactions with Sp2, Sp4, and KLF5.
目的。内皮组织型纤溶酶原激活物(t-PA)释放是保护循环系统免受闭塞性血栓形成影响的关键反应。我们已经表明,t-PA基因受到表观遗传调控,并且被组蛋白脱乙酰酶(HDAC)抑制剂丙戊酸(VPA)极大地诱导。我们现在研究了已知的t-PA启动子调控元件的参与情况,并评估了潜在相互作用的转录因子/辅因子的依赖性。方法。将一个报告载体转染到HT-1080和人脐静脉内皮细胞(HUVECs)中,该报告载体的插入片段在t-PA启动子的CRE或GC框II或GC框III元件处分别发生突变,并用VPA进行刺激。用针对组蛋白乙酰转移酶(HAT)和Sp/KLF家族中选定转录因子的小干扰RNA(siRNA)作用于HUVECs。结果。在CRE突变的构建体中观察到完整的VPA反应,而GC框II和III的突变分别使HT-1080中的诱导幅度降低54%和79%,在HUVECs中降低49%和50%。在Sp2、Sp4和KLF5缺失后,观察到t-PA mRNA的诱导减弱。KLF2和p300(HAT)被确定为基础t-PA表达的正调节因子,而Sp4和KLF9为负调节因子。结论。VPA诱导的t-PA表达依赖于t-PA启动子中的近端GC框,并且可能涉及与Sp2、Sp4和KLF5的相互作用。