Institute of Molecular Medicine and Experimental Immunology, University Hospital Bonn, Bonn, Germany.
Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia.
J Immunol. 2024 Sep 15;213(6):865-875. doi: 10.4049/jimmunol.2400041.
Chronic inflammasome activation in mononuclear phagocytes (MNPs) promotes fibrosis in various tissues, including the kidney. The cellular and molecular links between the inflammasome and fibrosis are unclear. To address this question, we fed mice lacking various immunological mediators an adenine-enriched diet, which causes crystal precipitation in renal tubules, crystal-induced inflammasome activation, and renal fibrosis. We found that kidney fibrosis depended on an intrarenal inflammasome-dependent type 3 immune response driven by its signature transcription factor Rorc (retinoic acid receptor-related orphan receptor C gene), which was partially carried out by type 3 innate lymphoid cells (ILC3s). The role of ILCs in the kidney is less well known than in other organs, especially that of ILC3. In this article, we describe that depletion of ILCs or genetic deficiency for Rorc attenuated kidney inflammation and fibrosis. Among the inflammasome-derived cytokines, only IL-1β expanded ILC3 and promoted fibrosis, whereas IL-18 caused differentiation of NKp46+ ILC3. Deficiency of the type 3 maintenance cytokine, IL-23, was more protective than IL-1β inhibition, which may be explained by the downregulation of the IL-1R, but not of the IL-23R, by ILC3 early in the disease, allowing persistent sensing of IL-23. Mechanistically, ILC3s colocalized with renal MNPs in vivo as shown by multiepitope-ligand cartography. Cell culture experiments indicated that renal ILC3s caused renal MNPs to increase TGF-β production that stimulated fibroblasts to produce collagen. We conclude that ILC3s link inflammasome activation with kidney inflammation and fibrosis and are regulated by IL-1β and IL-23.
单核吞噬细胞(MNPs)中的慢性炎症小体激活可促进包括肾脏在内的各种组织的纤维化。炎症小体与纤维化之间的细胞和分子联系尚不清楚。为了解决这个问题,我们给缺乏各种免疫介质的小鼠喂食富含腺嘌呤的饮食,这种饮食会导致肾脏小管中的晶体沉淀、晶体诱导的炎症小体激活和肾脏纤维化。我们发现,肾脏纤维化依赖于肾内炎症小体依赖性的 3 型免疫反应,该反应由其特征性转录因子 Rorc(维甲酸受体相关孤儿受体 C 基因)驱动,部分由 3 型固有淋巴细胞(ILC3)完成。ILC 在肾脏中的作用不如在其他器官中那么明显,尤其是 ILC3。在本文中,我们描述了耗尽 ILC 或基因缺陷 Rorc 可减轻肾脏炎症和纤维化。在炎症小体衍生的细胞因子中,只有 IL-1β 可扩增 ILC3 并促进纤维化,而 IL-18 可引起 NKp46+ILC3 的分化。与 IL-1β 抑制相比,缺乏 3 型维持细胞因子 IL-23 具有更强的保护作用,这可能是由于在疾病早期,ILC3 下调了 IL-1R,但没有下调 IL-23R,从而使 IL-23 持续感知。从机制上讲,正如多表位配体图谱所示,ILC3 在体内与肾脏 MNPs 共定位。细胞培养实验表明,肾脏 ILC3 导致肾脏 MNPs 增加 TGF-β 的产生,刺激成纤维细胞产生胶原。我们得出结论,ILC3 将炎症小体激活与肾脏炎症和纤维化联系起来,并受 IL-1β 和 IL-23 的调节。