巨噬细胞和树突状细胞发育和功能的时空适应性。

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2022-04-26 Epub Date: 2022-02-07 DOI:10.1146/annurev-immunol-101320-031931
Antoine Roquilly, Justine D Mintern, Jose A Villadangos
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引用次数: 18

摘要

巨噬细胞和常规树突状细胞(cDCs)分布在全身,维持组织稳态和自我耐受,协调先天和适应性免疫,抵抗感染和癌症。由于它们相互补充,了解它们如何合作以及整合它们的功能的机制是很重要的。两者都暴露于共生微生物、病原体和其他环境挑战中,这些挑战在解剖位置和时间上差异很大。为了适应这些变化的条件,巨噬细胞和cdc在其生命周期的不同阶段获得时空适应性(sta),这决定了它们如何对感染做出反应。因先前感染而获得的STAs可导致对感染的反应性增强,称为训练,或反应性降低,称为麻痹,在极端情况下可导致免疫抑制。了解巨噬细胞和cdc获得sta的发育阶段和位置,以及参与其诱导的分子和细胞参与者,可能为利用其有益结果并避免或逆转其有害影响提供机会。在这里,我们回顾了目前对巨噬细胞和cDC发展、生命周期、功能以及感染前、感染中和感染后STA获取的了解。我们提出了一个统一的框架来解释这两种细胞类型如何调整它们的活动以适应不断变化的空间和时间条件,以协调它们的免疫监视功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatiotemporal Adaptations of Macrophage and Dendritic Cell Development and Function.

Macrophages and conventional dendritic cells (cDCs) are distributed throughout the body, maintaining tissue homeostasis and tolerance to self and orchestrating innate and adaptive immunity against infection and cancer. As they complement each other, it is important to understand how they cooperate and the mechanisms that integrate their functions. Both are exposed to commensal microbes, pathogens, and other environmental challenges that differ widely among anatomical locations and over time. To adjust to these varying conditions, macrophages and cDCs acquire spatiotemporal adaptations (STAs) at different stages of their life cycle that determine how they respond to infection. The STAs acquired in response to previous infections can result in increased responsiveness to infection, termed training, or in reduced responses, termed paralysis, which in extreme cases can cause immunosuppression. Understanding the developmental stage and location where macrophages and cDCs acquire their STAs, and the molecular and cellular players involved in their induction, may afford opportunities to harness their beneficial outcomes and avoid or reverse their deleterious effects. Here we review our current understanding of macrophage and cDC development, life cycle, function, and STA acquisition before, during, and after infection.We propose a unified framework to explain how these two cell types adjust their activities to changing conditions over space and time to coordinate their immunosurveillance functions.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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