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一个核受体图谱:巨噬细胞活化

A Nuclear Receptor Atlas: macrophage activation.

作者信息

Barish Grant D, Downes Michael, Alaynick William A, Yu Ruth T, Ocampo Corinne B, Bookout Angie L, Mangelsdorf David J, Evans Ronald M

机构信息

Howard Hughes Medical Institute, The Salk Institute for Biological Studies, P.O. Box 85800, San Diego, California 92186-5800, USA.

出版信息

Mol Endocrinol. 2005 Oct;19(10):2466-77. doi: 10.1210/me.2004-0529. Epub 2005 Jul 28.

Abstract

Macrophage activation is an essential cellular process underlying innate immunity, enabling the body to combat bacteria and other pathogens. In addition to host defense, activated macrophages play a central role in atherogenesis, autoimmunity, and a variety of inflammatory diseases. As members of the Nuclear Receptor Signaling Atlas (NURSA) program, we employed quantitative real-time PCR (qPCR) to provide a comprehensive assessment of changes in expression of the 49 members of the murine nuclear receptor superfamily. In this study, we have identified a network of 28 nuclear receptors associated with the activation of bone marrow-derived macrophages by lipopolysaccharide or the prototypic cytokine interferon gamma. More than half of this network is deployed in three intricate and highly scripted temporal phases that are unique for each activator. Thus, early receptors whose expression peaks within 4 h after lipopolysaccharide exposure, such as glucocorticoid receptor, peroxisome proliferator-activated receptor gamma, and neuronal growth factor 1B, are found as late rising markers of the interferon gamma cascade, occurring 16 h or later. The discovery of precise serial expression patterns reveals that macrophage activation is the product of an underlying process that impacts the genome within minutes and identifies a collection of new therapeutic targets for controlling inflammation by disruption of presumptive regulatory cascades.

摘要

巨噬细胞激活是固有免疫的一个基本细胞过程,使机体能够对抗细菌和其他病原体。除了宿主防御外,活化的巨噬细胞在动脉粥样硬化、自身免疫和多种炎症性疾病中发挥核心作用。作为核受体信号图谱(NURSA)项目的成员,我们采用定量实时PCR(qPCR)对小鼠核受体超家族49个成员的表达变化进行了全面评估。在本研究中,我们鉴定出一个由28个核受体组成的网络,这些核受体与脂多糖或典型细胞因子干扰素γ激活骨髓来源的巨噬细胞有关。该网络一半以上的成员分布在三个复杂且高度有序的时间阶段,每个激活剂的阶段都是独特的。因此,脂多糖暴露后4小时内表达达到峰值的早期受体,如糖皮质激素受体、过氧化物酶体增殖物激活受体γ和神经生长因子1B,在干扰素γ级联反应中却是后期上升的标志物,出现在16小时或更晚。精确的序列表达模式的发现表明,巨噬细胞激活是一个在数分钟内影响基因组的潜在过程的产物,并确定了一系列通过破坏假定的调节级联反应来控制炎症的新治疗靶点。

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