先天免疫系统
重编程
免疫
免疫学
表观遗传学
生物
白色念珠菌
免疫系统
细胞
微生物学
遗传学
基因
作者
Siroon Bekkering,Leo A. B. Joosten,J.W.M. van der Meer,Mihai G. Netea,Niels P. Riksen
标识
DOI:10.1097/mol.0000000000000023
摘要
Monocytes/macrophages play a decisive role in the development and progression of atherosclerosis. It is currently unknown what stimuli initiate and orchestrate the activation of these cells in atherogenesis. In this review, we postulate that the novel concept of 'trained immunity' modulates the development and progression of atherosclerosis.Recently, results from our laboratory challenged the current paradigm that innate immunity is static and does not have an immunological memory. Stimulation by various microbial products, including Candida albicans and bacille Calmette-Guérin, appeared to bring monocytes into a long-term enhanced functional state, showing a stronger proinflammatory response to a second stimulus. This 'trained immunity' was mediated by increased and stable histone methylation.We describe the hypothesis that this functional reprogramming of monocytes, either by microbial products or by metabolic products, contributes to atherogenesis and propose epigenetic reprogramming of monocytes as a novel pharmacological target for preventing or treating atherosclerosis in the future.
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