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本文引用的文献

1
Nonclassical patrolling monocyte function in the vasculature.血管系统中非经典巡逻单核细胞的功能。
Arterioscler Thromb Vasc Biol. 2015 Jun;35(6):1306-16. doi: 10.1161/ATVBAHA.114.304650. Epub 2015 Apr 2.
2
Intravital live cell triggered imaging system reveals monocyte patrolling and macrophage migration in atherosclerotic arteries.活体活细胞触发成像系统揭示了动脉粥样硬化动脉中的单核细胞巡逻和巨噬细胞迁移。
J Biomed Opt. 2015 Feb;20(2):26005. doi: 10.1117/1.JBO.20.2.026005.
3
Nr4a1-dependent Ly6C(low) monocytes monitor endothelial cells and orchestrate their disposal.Nr4a1 依赖性 Ly6C(low) 单核细胞监测内皮细胞并协调其清除。
Cell. 2013 Apr 11;153(2):362-75. doi: 10.1016/j.cell.2013.03.010.
4
Fate mapping reveals origins and dynamics of monocytes and tissue macrophages under homeostasis.命运图谱揭示了稳态下单核细胞和组织巨噬细胞的起源和动态。
Immunity. 2013 Jan 24;38(1):79-91. doi: 10.1016/j.immuni.2012.12.001. Epub 2012 Dec 27.
5
NR4A1 (Nur77) deletion polarizes macrophages toward an inflammatory phenotype and increases atherosclerosis.NR4A1(Nur77)缺失使巨噬细胞向炎症表型极化,并增加动脉粥样硬化。
Circ Res. 2012 Feb 3;110(3):416-27. doi: 10.1161/CIRCRESAHA.111.253377. Epub 2011 Dec 22.
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The transcription factor NR4A1 (Nur77) controls bone marrow differentiation and the survival of Ly6C- monocytes.转录因子 NR4A1(Nur77)控制骨髓分化和 Ly6C-单核细胞的存活。
Nat Immunol. 2011 Jul 3;12(8):778-85. doi: 10.1038/ni.2063.
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Comparison of gene expression profiles between human and mouse monocyte subsets.人源和鼠源单核细胞亚群基因表达谱的比较。
Blood. 2010 Jan 21;115(3):e10-9. doi: 10.1182/blood-2009-07-235028. Epub 2009 Nov 12.
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Regulation of the migration and survival of monocyte subsets by chemokine receptors and its relevance to atherosclerosis.趋化因子受体对单核细胞亚群迁移和存活的调节及其与动脉粥样硬化的相关性。
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Chapter 16. Two-photon microscopy and multidimensional analysis of cell dynamics.第16章. 双光子显微镜与细胞动力学的多维分析
Methods Enzymol. 2009;461:349-78. doi: 10.1016/S0076-6879(09)05416-0.
10
Monitoring of blood vessels and tissues by a population of monocytes with patrolling behavior.具有巡逻行为的单核细胞群体对血管和组织的监测。
Science. 2007 Aug 3;317(5838):666-70. doi: 10.1126/science.1142883.

雪貂视角下的单核细胞巡逻

A Polecat's View of Patrolling Monocytes.

机构信息

From the Department of Pathology and Immunology, Washington University in St. Louis, MO.

出版信息

Circ Res. 2017 May 26;120(11):1699-1701. doi: 10.1161/CIRCRESAHA.117.311021.

DOI:10.1161/CIRCRESAHA.117.311021
PMID:28546349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5546358/
Abstract

A major obstacle to intravital visualization of inflammatory processes within large arteries is the motion of vessels that occurs near the beating heart. In this issue, Quintar et al. apply ILTIS, the German word for the European polecat that serves as an acronym for Intravital Live-cell Triggered Imaging System, to capture the most sophisticated images of inflammatory cell dynamics in the arterial vasculature to date, by timing data acquisition to a consistent point in every heartbeat. The authors show that patrolling nonclassical monocytes scan endothelium in plaque-prone areas, much as they have been described to elsewhere. The inability of these monocytes to patrol arteries leads to heightened endothelial damage within the artery. In this way, nonclassical monocytes safeguard against plaque development and progression.

摘要

在跳动的心脏附近,大动脉内部炎症过程的活体可视化存在一个主要障碍,即血管的运动。在本期中,Quintar 等人应用了 ILTIS,这是德语中欧鼬的缩写,代表活体活细胞触发成像系统,通过将数据采集与每个心跳的一致点同步,来捕获迄今为止动脉脉管系统中炎症细胞动力学的最复杂图像。作者表明,巡逻的非经典单核细胞扫描斑块易损区的内皮细胞,就像在其他地方描述的那样。这些单核细胞不能巡逻动脉,导致动脉内皮细胞损伤加剧。通过这种方式,非经典单核细胞可以防止斑块的形成和发展。