Medical University of Vienna, Center for Medical Biochemistry, Max Perutz Labs Vienna, Campus Vienna Biocenter, 1030 Vienna, Austria.
Department of Internal Medicine II, Infectious Diseases, Immunology, Rheumatology, and Pneumology, Medical University of Innsbruck, 6020 Innsbruck, Austria; Christian Doppler Laboratory for Iron Metabolism and Anemia Research, 6020 Innsbruck, Austria.
Cell Host Microbe. 2020 Mar 11;27(3):454-466.e8. doi: 10.1016/j.chom.2020.01.023. Epub 2020 Feb 18.
Type I interferons (IFNs-I) fulfil multiple protective functions during pathogenic infections, but they can also cause detrimental effects and enhance immunopathology. Here, we report that IFNs-I promote the dysregulation of iron homeostasis in macrophages during systemic infections with the intracellular pathogen Candida glabrata, leading to fungal survival and persistence. By engaging JAK1, IFNs-I disturb the balance of the transcriptional activator NRF2 and repressor BACH1 to induce downregulation of the key iron exporter Fpn1 in macrophages. This leads to enhanced iron accumulation in the phagolysosome and failure to restrict fungal access to iron pools. As a result, C. glabrata acquires iron via the Sit1/Ftr1 iron transporter system, facilitating fungal intracellular replication and immune evasion. Thus, IFNs-I are central regulators of iron homeostasis, which can impact infection, and restricting iron bioavailability may offer therapeutic strategies to combat invasive fungal infections.
I 型干扰素 (IFN-I) 在病原体感染过程中发挥多种保护作用,但也可能产生有害影响并增强免疫病理学。在这里,我们报告 IFN-I 在系统性感染细胞内病原体光滑念珠菌时促进巨噬细胞中铁稳态的失调,导致真菌存活和持续存在。通过与 JAK1 结合,IFN-I 扰乱转录激活因子 NRF2 和抑制因子 BACH1 的平衡,诱导巨噬细胞中铁输出蛋白 Fpn1 的下调。这导致吞噬体中的铁积累增加,并不能限制真菌对铁库的获取。结果,C. glabrata 通过 Sit1/Ftr1 铁转运系统获取铁,促进真菌的细胞内复制和免疫逃避。因此,IFN-I 是铁稳态的核心调节剂,它可以影响感染,限制铁的生物利用度可能为治疗侵袭性真菌感染提供策略。