Toll-like receptor signaling in teleosts.

IF 8 2区 生物学 Q1 BIOLOGY Science China Life Sciences Pub Date : 2025-02-14 DOI:10.1007/s11427-024-2822-5
Jianguo Su
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Abstract

Toll-like receptors (TLRs) sit at the top of the immune system pyramid. They form a paramount family of immune sentinels capable of sensing diverse microbe-associated molecular patterns (MAPMs), danger/damage-associated molecular patterns (DAMPs), and other signals. These perceptions trigger immediate innate immunity and instruct subsequent adaptive immunity. TLRs are highly glycosylated type I transmembrane glycoproteins that share a conserved tripartite domain architecture (LRR, TM and TIR domains), classified into six subfamilies (TLR1, TLR3, TLR4, TLR5, TLR7, TLR11) in vertebrates. Upon ligand engagement, TLRs form homodimers or heterodimers to activate immune responses via SMOCs, orchestrated by intrinsic and pathogen-directed negative regulators, glycosylation modification, etc. TLR signaling culminates in the production of inflammatory cytokines, interferons, inflammasomes, immune cell activation, apoptosis, etc. Teleosts, as the largest and most diverse group among the extant vertebrates, manifest important economic value and are crucial for understanding the evolution of vertebrate immunity. To date, teleosts contain 20 TLRs (TLR1-5, TLR7-9, TLR13, TLR14, TLR18-23, TLR25-28) with expansions and losses in different species, and most of them possess more or less variants. Almost all teleostean TLRs localize in organelles, such as endosomes and lysosomes, sensing not only pathogens and DAMPs but also trophic factors and environmental stresses (hypoxia, temperature, microplastics, etc.). Most ligands for TLRs remain undetermined in teleosts. The adaptors consist of MyD88, TIRAP, TRIF, SARM1, BCAP and SCIMP, but without TRAM; however, half of the corresponding relationships between TLRs and adaptors remain unknown in teleosts. Neofunctionalization often emerges during evolution in teleostean TLRs. Here, a systematic review of TLR signaling in teleosts, from the perspective of comparative immunology, presents the current understanding of the functions and mechanisms of teleosts. Additionally, it provides strong evidence of a divergent TLR signaling repertoire with the species-specific variation among teleosts. These are expected to benefit novel adjuvants, aquaculture, fish immunology, and comparative immunology.

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Toll 样受体(TLRs)位于免疫系统金字塔的顶端。它们组成了一个重要的免疫哨兵家族,能够感知各种微生物相关分子模式(MAPM)、危险/损伤相关分子模式(DAMP)和其他信号。这些感知会立即触发先天性免疫,并指导随后的适应性免疫。TLRs 是高度糖基化的 I 型跨膜糖蛋白,具有保守的三方结构域(LRR、TM 和 TIR 结构域),在脊椎动物中分为六个亚家族(TLR1、TLR3、TLR4、TLR5、TLR7 和 TLR11)。配体接合后,TLR 形成同源二聚体或异源二聚体,通过 SMOCs 激活免疫反应,SMOCs 由内在和病原体导向的负调控因子、糖基化修饰等协调。TLR 信号最终产生炎性细胞因子、干扰素、炎性体、免疫细胞活化和凋亡等。远洋脊椎动物是现存脊椎动物中最大和最多样化的类群,具有重要的经济价值,对于了解脊椎动物免疫的进化至关重要。迄今为止,远洋鱼类包含 20 种 TLRs(TLR1-5、TLR7-9、TLR13、TLR14、TLR18-23、TLR25-28),在不同物种中存在扩展和缺失,而且大多数 TLRs 或多或少都有变种。几乎所有远缘动物的 TLR 都定位于细胞器(如内体和溶酶体),不仅能感知病原体和 DAMP,还能感知营养因子和环境压力(缺氧、温度、微塑料等)。在远缘动物中,TLRs 的大多数配体仍未确定。适配体包括MyD88、TIRAP、TRIF、SARM1、BCAP和SCIMP,但不包括TRAM;然而,在远洋鱼类中,TLRs与适配体之间的对应关系有一半仍然未知。在远足目动物 TLRs 的进化过程中,经常会出现新功能化现象。在此,我们从比较免疫学的角度系统回顾了远足目动物的 TLR 信号转导,介绍了目前对远足目动物的功能和机制的理解。此外,它还提供了强有力的证据,证明TLR信号曲目与远洋鱼类的物种特异性差异不同。这些都将有益于新型佐剂、水产养殖、鱼类免疫学和比较免疫学。
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来源期刊
CiteScore
15.10
自引率
8.80%
发文量
2907
审稿时长
3.2 months
期刊介绍: Science China Life Sciences is a scholarly journal co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China, and it is published by Science China Press. The journal is dedicated to publishing high-quality, original research findings in both basic and applied life science research.
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