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巨噬细胞分化与心血管疾病中的固有免疫记忆

Innate immune memory in macrophage differentiation and cardiovascular diseases.

作者信息

Nakayama Yukiteru, Fujiu Katsuhito

机构信息

Department of Cardiovascular Medicine, the University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.

Department of Advanced Cardiology, the University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo, 113-8655, Japan.

出版信息

Inflamm Regen. 2025 Jun 3;45(1):17. doi: 10.1186/s41232-025-00382-5.

Abstract

Innate immune memory (trained immunity) refers to the ability of innate immune cells, such as monocytes and macrophages, to retain a long-term imprint of a prior stimulus through epigenetic and metabolic adaptations, enabling amplified responses upon restimulation. Recent studies have classified innate immune memory into central and peripheral types. Central innate immune memory originates in hematopoietic stem cells (HSCs) within the bone marrow, where epigenetic reprogramming generates a sustained inflammatory bias, contributing to chronic diseases such as atherosclerosis, heart failure, and stroke. Peripheral innate immune memory occurs in monocytes or macrophages that acquire heightened responsiveness after repeated exposure to stimuli in peripheral tissues. This review explores the mechanisms underlying both central and peripheral innate immune memory, their roles in chronic inflammatory diseases, focusing on cardiovascular diseases, and potential strategies to target innate immune memory for therapeutic purposes. Advancing the understanding of these processes could facilitate the development of novel approaches to control inflammatory diseases and immune-related disorders.

摘要

固有免疫记忆(训练性免疫)是指固有免疫细胞(如单核细胞和巨噬细胞)通过表观遗传和代谢适应对先前刺激保留长期印记的能力,从而在再次刺激时能够产生放大反应。最近的研究将固有免疫记忆分为中枢型和外周型。中枢固有免疫记忆起源于骨髓中的造血干细胞(HSC),在那里表观遗传重编程产生持续的炎症倾向,导致诸如动脉粥样硬化、心力衰竭和中风等慢性疾病。外周固有免疫记忆发生在单核细胞或巨噬细胞中,这些细胞在反复接触外周组织中的刺激后获得增强的反应性。本综述探讨了中枢和外周固有免疫记忆的潜在机制、它们在慢性炎症性疾病(重点是心血管疾病)中的作用以及针对固有免疫记忆进行治疗的潜在策略。加深对这些过程的理解可能有助于开发控制炎症性疾病和免疫相关疾病的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72c0/12131520/d1b9412e0f0f/41232_2025_382_Fig1_HTML.jpg

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