巨噬细胞中的补体 C5a 受体信号通过激活 mTOR 途径增强训练有素的免疫力

IF 4.3 4区 医学 Q2 IMMUNOLOGY Immune Network Pub Date : 2024-06-05 eCollection Date: 2024-08-01 DOI:10.4110/in.2024.24.e24
Eun-Hyeon Shim, Sae-Hae Kim, Doo-Jin Kim, Yong-Suk Jang
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引用次数: 0

摘要

免疫细胞中的补体 C5a 受体(C5aR)信号具有多种功能,可根据配体类型诱导炎症或抗炎反应。据报道,Co1 肽(SFHQLPARSRPLP)能激活树突状细胞中的 C5aR 信号。我们研究了 C5aR 信号通过 Co1 肽对巨噬细胞的影响。在腹腔巨噬细胞中,C5aR 和 Co1 肽之间的相互作用激活了 mTOR 通路,导致促炎细胞因子的产生。考虑到mTOR信号与巨噬细胞训练中的IL-6和TNF-α密切相关,我们的研究结果表明,Co1肽扩大了β-葡聚糖诱导的训练免疫。总之,这项研究强调了训练免疫中 C5aR 信号转导以前未被重视的一个方面,并认为 Co1 肽是一种潜在的有效免疫调节剂,可增强训练免疫。
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Complement C5a Receptor Signaling in Macrophages Enhances Trained Immunity Through mTOR Pathway Activation.

Complement C5a receptor (C5aR) signaling in immune cells has various functions, inducing inflammatory or anti-inflammatory responses based on the type of ligand present. The Co1 peptide (SFHQLPARSRPLP) has been reported to activate C5aR signaling in dendritic cells. We investigated the effect of C5aR signaling via the Co1 peptide on macrophages. In peritoneal macrophages, the interaction between C5aR and the Co1 peptide activated the mTOR pathway, resulting in the production of pro-inflammatory cytokines. Considering the close associations of mTOR signaling with IL-6 and TNF-α in macrophage training, our findings indicate that the Co1 peptide amplifies β-glucan-induced trained immunity. Overall, this research highlights a previously underappreciated aspect of C5aR signaling in trained immunity, and posits that the Co1 peptide is a potentially effective immunomodulator for enhancing trained immunity.

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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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