Division of Immunology and Molecular Biology, Cancer Research Institute, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan; Institute for Frontier Science Initiative (InFiniti), Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
Division of Immunology and Molecular Biology, Cancer Research Institute, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
Cell Rep. 2021 Mar 23;34(12):108887. doi: 10.1016/j.celrep.2021.108887.
IL-1α serves as a pro-inflammatory cytokine. Although pro-IL-1α has cytokine activity, proteolytic maturation increases its potency and release from cells. IL-1α maturation occurs in a caspase-1-dependent manner following inflammasome activation. However, pro-IL-1α is not a substrate of caspase-1, and it remains unclear what mediates the maturation of this cytokine downstream of inflammasomes. Here, we show that gasdermin D (GSDMD), an executor of pyroptosis, is required for the rapid induction of IL-1α maturation by non-particulate inflammasome activators. Ablation of GSDMD abrogates the maturation of IL-1α, but not of IL-1β. Inflammasome-induced maturation of IL-1α relies on extracellular Ca and calpains. Ca influx and calpain activation are induced in a GSDMD-dependent manner. Glycine, which inhibits cell lysis, but not GSDMD pore formation, does not affect IL-1α maturation. These results suggest that during inflammasome activation, GSDMD processed by caspase-1 forms plasma membrane pores that mediate Ca influx, resulting in the calpain-dependent maturation of IL-1α.
IL-1α 作为一种促炎细胞因子。虽然前体 IL-1α 具有细胞因子活性,但蛋白水解成熟会增加其效力并从细胞中释放。IL-1α 的成熟是在炎症小体激活后以半胱天冬酶-1(caspase-1)依赖的方式发生的。然而,前体 IL-1α 不是 caspase-1 的底物,目前尚不清楚炎症小体下游什么介导了这种细胞因子的成熟。在这里,我们表明,gasdermin D(GSDMD),细胞焦亡的执行者,是无颗粒炎症小体激活物快速诱导 IL-1α 成熟所必需的。GSDMD 的缺失会消除 IL-1α 的成熟,但不会消除 IL-1β。炎症小体诱导的 IL-1α 成熟依赖于细胞外 Ca 和钙蛋白酶。Ca 内流和钙蛋白酶激活以 GSDMD 依赖的方式诱导。甘氨酸抑制细胞裂解,但不抑制 GSDMD 孔形成,不影响 IL-1α 的成熟。这些结果表明,在炎症小体激活期间,被 caspase-1 处理的 GSDMD 形成质膜孔,介导 Ca 内流,导致依赖钙蛋白酶的 IL-1α 成熟。