D'Ignazio Laura, Batie Michael, Rocha Sonia
Center for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee DD15EH, UK.
Department of Biochemistry, Institute of Integrative Biology, University of Liverpool, Liverpool L697ZB, UK.
Cells. 2018 Aug 8;7(8):102. doi: 10.3390/cells7080102.
Non-canonical NF-κB signalling plays important roles in the development and function of the immune system but it also is deregulated in a number of inflammatory diseases. Although, NF-κB and HIF crosstalk has been documented, this has only been described following canonical NF-κB stimulation, involving RelA/p50 and the HIF-1 dimer. Here, we report that the non-canonical inducer TNFSF14/LIGHT leads to HIF induction and activation in cancer cells. We demonstrate that only HIF-2α is induced at the transcriptional level following non-canonical NF-κB activation, via a mechanism that is dependent on the p52 subunit. Furthermore, we demonstrate that p52 can bind to the HIF-2α promoter in cells. These results indicate that non-canonical NF-κB can lead to HIF signalling implicating HIF-2α as one of the downstream effectors of this pathway in cells.
非经典NF-κB信号通路在免疫系统的发育和功能中发挥着重要作用,但在许多炎症性疾病中也会失调。尽管已经有文献记载了NF-κB和HIF的相互作用,但这仅在经典NF-κB刺激后被描述,涉及RelA/p50和HIF-1二聚体。在此,我们报告非经典诱导剂TNFSF14/LIGHT可导致癌细胞中HIF的诱导和激活。我们证明,在非经典NF-κB激活后,仅HIF-2α在转录水平上被诱导,其机制依赖于p52亚基。此外,我们证明p52可以在细胞中与HIF-2α启动子结合。这些结果表明,非经典NF-κB可导致HIF信号传导,这意味着HIF-2α是该通路在细胞中的下游效应器之一。