Molecular regulation of the PAI-1 gene by hypoxia: contributions of Egr-1, HIF-1 alpha, and C/EBP alpha

摘要

Hypoxia, as occurs during tissue ischemia, tips the natural anticoagulant/procoagulant balance of the endovascular wall to favor activation of coagulation. Plasminogen activator inhibitor-1 (PAI-1) is an important factor suppressing fibrinolysis under conditions of low oxygen tension. We previously reported that hypoxia induced PAI-1 mRNA and antigen expression in murine macrophages secondary to increased de novo transcription as well as increased mRNA stability. We now show in RAW264.7 murine macrophages that the transcription factors early growth response gene-1 (Egr-1), hypoxia-inducible factor-1 alpha (HIF-1 alpha), and CCAAT/enhancer binding protein cl (C/EBP alpha) are quickly activated in hypoxia and are responsible for transcription and expression of PAI-1. Murine PAI-1 promoter constructs, including Egr, HIF-1 alpha, and/or C/EBP alpha binding sites, were transfected into RAW 264.7 murine macrophages. To identify the relative importance of each of these putative hypoxia-responsive elements, cells were exposed to normobaric hypoxia, and transcriptional activity was recorded. At 16 h of hypoxic exposure, murine PAW promoter deletion constructs that included Egr, HIF-1 alpha, and/or C/EBP alpha binding sites demonstrated increased transcriptional activity. Mutation of each of these three murine PAI-1 promoter sites (or a combination of them) resulted in a marked reduction in hypoxia sensitivity as detected by transcriptional analysis. Functional data obtained using P-32-labeled Egr, HIF-1 alpha response element (HRE), and C/EBP alpha oligonucleotides revealed induction of DNA binding activity in nuclear extracts from hypoxic RAW cells, with supershift analysis confirming activation of Egr-1, HIF-1 alpha, or C/EBP alpha. ChIP analysis confirmed the authenticity of these interactions as each of these transcription factors binds to chromatin under hypoxic conditions. Further, the induction of PAI-1 by Egr-I, HIF-1 alpha, or C/EBP alpha was replicated in primary peritoneal macrophages. These data suggest that although HIF-1 alpha appears to dominate the PAI-1 transcriptional response in hypoxia, Egr-1 and C/EBP alpha greatly augment this response and can do so independent of HIF-1 alpha or each other. These studies are relevant to ischemic up-regulation of the PAI-1 gene and consequent accrual of microvascular thrombus under ischemic conditions.