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巨噬细胞中补体C5a受体信号通过激活mTOR途径增强训练免疫。

Complement C5a Receptor Signaling in Macrophages Enhances Trained Immunity Through mTOR Pathway Activation.

作者信息

Shim Eun-Hyeon, Kim Sae-Hae, Kim Doo-Jin, Jang Yong-Suk

机构信息

Innovative Research and Education Center for Integrated Bioactive Materials and the Department of Bioactive Material Sciences, Jeonbuk National University, Jeonju 54896, Korea.

Department of Bioscience, University of Science and Technology (UST), Daejeon 34113, Korea.

出版信息

Immune Netw. 2024 Jun 5;24(4):e24. doi: 10.4110/in.2024.24.e24. eCollection 2024 Aug.

Abstract

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.

摘要

免疫细胞中的补体C5a受体(C5aR)信号传导具有多种功能,根据存在的配体类型诱导炎症或抗炎反应。据报道,Co1肽(SFHQLPARSRPLP)可激活树突状细胞中的C5aR信号传导。我们研究了通过Co1肽的C5aR信号传导对巨噬细胞的影响。在腹膜巨噬细胞中,C5aR与Co1肽之间的相互作用激活了mTOR途径,导致促炎细胞因子的产生。考虑到mTOR信号传导与巨噬细胞训练中IL-6和TNF-α的密切关联,我们的研究结果表明Co1肽增强了β-葡聚糖诱导的训练免疫。总体而言,这项研究突出了训练免疫中C5aR信号传导一个以前未被充分认识的方面,并提出Co1肽是增强训练免疫的一种潜在有效的免疫调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6fe/11377950/94c4f8445801/in-24-e24-g001.jpg

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