IL-1 Receptor Dynamics in Immune Cells: Orchestrating Immune Precision and Balance.

IF 4.3 4区 医学 Q2 IMMUNOLOGY
Immune Network Pub Date : 2024-05-29 eCollection Date: 2024-06-01 DOI:10.4110/in.2024.24.e21
Dong Hyun Kim, Won-Woo Lee
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Abstract

IL-1, a pleiotropic cytokine with profound effects on various cell types, particularly immune cells, plays a pivotal role in immune responses. The proinflammatory nature of IL-1 necessitates stringent control mechanisms of IL-1-mediated signaling at multiple levels, encompassing transcriptional and translational regulation, precursor processing, as well as the involvement of a receptor accessory protein, a decoy receptor, and a receptor antagonist. In T-cell immunity, IL-1 signaling is crucial during both the priming and effector phases of immune reactions. The fine-tuning of IL-1 signaling hinges upon two distinct receptor types; the functional IL-1 receptor (IL-1R) 1 and the decoy IL-1R2, accompanied by ancillary molecules such as the IL-1R accessory protein (IL-1R3) and IL-1R antagonist. IL-1R1 signaling by IL-1β is critical for the differentiation, expansion, and survival of Th17 cells, essential for defense against extracellular bacteria or fungi, yet implicated in autoimmune disease pathogenesis. Recent investigations emphasize the physiological importance of IL-1R2 expression, particularly in its capacity to modulate IL-1-dependent responses within Tregs. The precise regulation of IL-1R signaling is indispensable for orchestrating appropriate immune responses, as unchecked IL-1 signaling has been implicated in inflammatory disorders, including Th17-mediated autoimmunity. This review provides a thorough exploration of the IL-1R signaling complex and its pivotal roles in immune regulation. Additionally, it highlights recent advancements elucidating the mechanisms governing the expression of IL-1R1 and IL-1R2, underscoring their contributions to fine-tuning IL-1 signaling. Finally, the review briefly touches upon therapeutic strategies targeting IL-1R signaling, with potential clinical applications.

免疫细胞中的 IL-1 受体动力学:协调免疫精确性和平衡。
IL-1 是一种对各类细胞,尤其是免疫细胞有深远影响的多效性细胞因子,在免疫反应中发挥着关键作用。IL-1 的促炎特性要求对 IL-1 介导的信号传导进行多层次的严格控制,包括转录和翻译调控、前体处理以及受体附属蛋白、诱饵受体和受体拮抗剂的参与。在 T 细胞免疫中,IL-1 信号在免疫反应的启动和效应阶段都至关重要。IL-1信号的微调取决于两种不同的受体类型:功能性IL-1受体(IL-1R)1和诱饵IL-1R2,以及辅助分子,如IL-1R附属蛋白(IL-1R3)和IL-1R拮抗剂。由 IL-1β 发出的 IL-1R1 信号对 Th17 细胞的分化、扩增和存活至关重要,是抵御细胞外细菌或真菌的关键,但也与自身免疫性疾病的发病机制有关。最近的研究强调了 IL-1R2 表达的生理重要性,尤其是其调节 Tregs 内 IL-1 依赖性反应的能力。IL-1R信号的精确调控对于协调适当的免疫反应是不可或缺的,因为不受控制的IL-1信号与炎症性疾病(包括Th17介导的自身免疫)有关。本综述深入探讨了 IL-1R 信号复合体及其在免疫调节中的关键作用。此外,它还重点介绍了最近在阐明 IL-1R1 和 IL-1R2 的表达机制方面取得的进展,强调了它们对 IL-1 信号微调的贡献。最后,综述简要介绍了针对 IL-1R 信号转导的治疗策略,以及潜在的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Immune Network
Immune Network Immunology and Microbiology-Immunology
CiteScore
2.90
自引率
3.30%
发文量
36
期刊介绍: Immune Network publishes novel findings in basic and clinical immunology and aims to provide a medium through which researchers in various fields of immunology can share and connect. The journal focuses on advances and insights into the regulation of the immune system and the immunological mechanisms of various diseases. Research that provides integrated insights into translational immunology is given preference for publication. All submissions are evaluated based on originality, quality, clarity, and brevity
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