Department of Laboratory Medicine, Affiliated Hospital of Jiangsu University, Zhenjiang, China.
International Genome Center, Jiangsu University, Zhenjiang, China.
Front Immunol. 2020 Nov 16;11:586613. doi: 10.3389/fimmu.2020.586613. eCollection 2020.
Dendritic cells (DCs) are specialized antigen-presenting cells that play a key role in immune homeostasis and the adaptive immune response. DC-induced immune tolerance or activation is strictly dependent on the distinct maturation stages and migration ability of DCs. Ubiquitination is a reversible protein post-translational modification process that has emerged as a crucial mechanism that regulates DC maturation and function. Recent studies have shown that ubiquitin enzymes, including E3 ubiquitin ligases and deubiquitinases (DUBs), are pivotal regulators of DC-mediated immune function and serve as potential targets for DC-based immunotherapy of immune-related disorders (e.g., autoimmune disease, infections, and tumors). In this review, we summarize the recent progress regarding the molecular mechanisms and function of ubiquitination in DC-mediated immune homeostasis and immune response.
树突状细胞(DCs)是一种专门的抗原呈递细胞,在免疫稳态和适应性免疫反应中发挥关键作用。DC 诱导的免疫耐受或激活严格依赖于 DC 的不同成熟阶段和迁移能力。泛素化是一种可逆的蛋白质翻译后修饰过程,已成为调节 DC 成熟和功能的关键机制。最近的研究表明,包括 E3 泛素连接酶和去泛素化酶(DUBs)在内的泛素酶是 DC 介导的免疫功能的关键调节剂,并且可以作为基于 DC 的免疫治疗免疫相关疾病(例如,自身免疫性疾病、感染和肿瘤)的潜在靶点。在这篇综述中,我们总结了泛素化在 DC 介导的免疫稳态和免疫反应中的分子机制和功能的最新进展。