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全会观点:单核吞噬细胞中组成性和诱导性基因表达的复杂性。

Plenary perspective: the complexity of constitutive and inducible gene expression in mononuclear phagocytes.

机构信息

The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Scotland, United Kingdom.

出版信息

J Leukoc Biol. 2012 Sep;92(3):433-44. doi: 10.1189/jlb.0312166. Epub 2012 Jul 5.

DOI:10.1189/jlb.0312166
PMID:22773680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3427611/
Abstract

Monocytes and macrophages differentiate from progenitor cells under the influence of colony-stimulating factors. Genome-scale data have enabled the identification of the set of genes that distinguishes macrophages from other cell types and the ways in which thousands of genes are regulated in response to pathogen challenge. Although there has been a focus on a small subset of lineage-enriched transcription factors, such as PU.1, more than one-half of the transcription factors in the genome can be expressed in macrophage lineage cells under some state of activation, and they interact in a complex network. The network architecture is conserved across species, but many of the target genes evolve rapidly and differ between mouse and human. The data and publication deluge related to macrophage biology require the development of new analytical tools and ways of presenting information in an accessible form.

摘要

单核细胞和巨噬细胞在集落刺激因子的影响下从祖细胞中分化而来。基因组规模的数据使我们能够识别出将巨噬细胞与其他细胞类型区分开来的基因集,以及数千个基因在应对病原体挑战时的调控方式。尽管人们一直关注一小部分谱系特异性转录因子,如 PU.1,但在某种激活状态下,基因组中超过一半的转录因子可以在巨噬细胞谱系细胞中表达,并且它们相互作用形成一个复杂的网络。该网络架构在物种间是保守的,但许多靶基因在进化上迅速变化,并且在小鼠和人类之间存在差异。与巨噬细胞生物学相关的数据和出版物如潮水般涌现,这需要开发新的分析工具和以易于访问的形式呈现信息的方法。

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本文引用的文献

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Biochim Biophys Acta. 2012 Jul;1824(7):938-45. doi: 10.1016/j.bbapap.2012.04.012. Epub 2012 May 8.
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Adult Langerhans cells derive predominantly from embryonic fetal liver monocytes with a minor contribution of yolk sac-derived macrophages.成人朗格汉斯细胞主要来源于胚胎胎肝中的单核细胞,少量来源于卵黄囊来源的巨噬细胞。
J Exp Med. 2012 Jun 4;209(6):1167-81. doi: 10.1084/jem.20120340. Epub 2012 May 7.
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The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation.集落刺激因子 1 受体配体白细胞介素 34 和集落刺激因子 1 表现出不同的发育性大脑表达模式,并调节神经祖细胞的维持和成熟。
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Structural basis for the dual recognition of helical cytokines IL-34 and CSF-1 by CSF-1R.IL-34 和 CSF-1 被 CSF-1R 双重识别的结构基础。
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Conservation and divergence in Toll-like receptor 4-regulated gene expression in primary human versus mouse macrophages.TLR4 调控的原代人源和鼠源巨噬细胞基因表达的保守性与差异性。
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