Department of Pathology and Immunology, School of Medicine, University of Geneva, 1211, Geneva 4, Switzerland; Division of Rheumatology, Department of Internal Medicine, University Hospital, 1211 Geneva 4, Switzerland.
Department of Pathology and Immunology, School of Medicine, University of Geneva, 1211, Geneva 4, Switzerland.
Cell Rep. 2019 Jul 2;28(1):21-29.e6. doi: 10.1016/j.celrep.2019.05.110.
Regulatory T cells (Tregs) play a crucial role in controlling autoimmune and inflammatory responses. Recent studies have demonstrated that dendritic cells (DCs) contribute to the homeostasis of peripheral Tregs. Autophagy, a critical pathway for cellular homeostasis, is active in DCs and is upregulated in different inflammatory conditions. We have shown that Tregs are expanded and have phenotypic alterations and impaired suppressive functions in mice with autophagy-deficient DCs. RNA profiling of Tregs revealed that autophagy in DCs is required to stabilize Treg expression signatures. This phenotype is linked to the downregulation of ICOS-Ligand expression in autophagy-deficient DCs, a consequence of the accumulation of ADAM10, the metalloproteinase responsible for its cleavage. Upon inflammation, in antigen-induced arthritis, mice with autophagy-deficient DCs exhibit increased synovial inflammation and cartilage and bone erosion correlating with Treg-to-Th17 conversion. Our data reveal a mechanism that couples autophagy deficiency in DCs to the function, homeostasis, and stability of Tregs.
调节性 T 细胞(Tregs)在控制自身免疫和炎症反应中起着至关重要的作用。最近的研究表明,树突状细胞(DCs)有助于外周 Tregs 的稳态。自噬是细胞稳态的关键途径,在 DCs 中活跃,并在不同的炎症条件下上调。我们已经表明,在自噬缺陷的 DCs 存在的情况下,Tregs 会扩增,并表现出表型改变和抑制功能受损。对 Tregs 的 RNA 分析表明,DCs 中的自噬对于稳定 Treg 的表达特征是必需的。这种表型与自噬缺陷的 DCs 中 ICOS-Ligand 表达的下调有关,这是负责其切割的金属蛋白酶 ADAM10 积累的结果。在炎症时,在抗原诱导的关节炎中,自噬缺陷的 DCs 存在时,滑膜炎症和软骨及骨侵蚀增加,与 Treg 向 Th17 转化相关。我们的数据揭示了一种机制,将 DCs 中的自噬缺陷与 Tregs 的功能、稳态和稳定性联系起来。