WPI Immunology Frontier Research Center (IFReC), Osaka University, Osaka 565-0871, Japan; Division of Cell Signaling, Okazaki Institute for Integrative Bioscience (National Institute for Physiological Sciences), National Institutes of Natural Sciences, Aichi 444-8787, Japan.
Department of Signal Transduction, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Cell Rep. 2020 Jul 14;32(2):107906. doi: 10.1016/j.celrep.2020.107906.
Zinc finger protein St18 was initially reported as candidate tumor suppressor gene, and also suggested that fibroblast St18 positively regulates NF-κB activation. Despite the pleiotropic functions of St18, little is known about its roles in macrophages. Here, we report that myeloid St18 is a potent inhibitor of VEGF-A. Mice lacking St18 in myeloid lineages exhibit increased retinal vasculature with enhanced serum VEGF-A concentrations. Despite the normal activation of NF-κB target genes, these mice are highly susceptible to LPS-induced shock, polymicrobial sepsis, and experimental colitis, accompanied by enhanced vascular and intestinal leakage. Pharmacological inhibition of VEGF signaling rescued the high mortality rate of myeloid-specific St18-deficient mice in response to inflammation. Mechanistically, St18 directly binds to Sp1 and attenuates its activity, leading to the suppression of Sp1 target gene VEGF-A. Using mouse genetic and pharmacological models, we reveal myeloid St18 as a critical septic death protector.
锌指蛋白 St18 最初被报道为候选肿瘤抑制基因,也表明成纤维细胞 St18 正向调节 NF-κB 激活。尽管 St18 具有多种功能,但人们对其在巨噬细胞中的作用知之甚少。在这里,我们报告髓系 St18 是 VEGF-A 的有效抑制剂。骨髓谱系中缺乏 St18 的小鼠表现出视网膜血管增多,血清 VEGF-A 浓度升高。尽管 NF-κB 靶基因的正常激活,但这些小鼠对 LPS 诱导的休克、多微生物败血症和实验性结肠炎高度敏感,伴有增强的血管和肠道渗漏。VEGF 信号转导的药理学抑制挽救了对炎症反应中骨髓特异性 St18 缺陷型小鼠的高死亡率。在机制上,St18 直接与 Sp1 结合并减弱其活性,导致 Sp1 靶基因 VEGF-A 的抑制。使用小鼠遗传和药理学模型,我们揭示了髓系 St18 作为一种关键的败血症死亡保护因子。