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Dual Detection of Nucleolytic and Proteolytic Markers of Lysosomal Cell Death: DNase II-Type Breaks and Cathepsin D.溶酶体细胞死亡的核酸酶解和蛋白酶解标志物的双重检测:DNase II型断裂和组织蛋白酶D
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本文引用的文献

1
Janus-faced microglia: beneficial and detrimental consequences of microglial phagocytosis.两面派的小胶质细胞:小胶质细胞吞噬作用的有益和有害后果。
Front Cell Neurosci. 2013 Jan 30;7:6. doi: 10.3389/fncel.2013.00006. eCollection 2013.
2
ROCK/Cdc42-mediated microglial motility and gliapse formation lead to phagocytosis of degenerating dopaminergic neurons in vivo.ROCK/Cdc42 介导的小胶质细胞运动和神经胶质突触形成导致体内退化多巴胺能神经元的吞噬作用。
Sci Rep. 2012;2:809. doi: 10.1038/srep00809. Epub 2012 Nov 8.
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Microglial cells contribute to endogenous brain defenses after acute neonatal focal stroke.小胶质细胞在急性新生儿局灶性脑卒中后有助于内源性脑防御。
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Fluorescent probes detecting the phagocytic phase of apoptosis: enzyme-substrate complexes of topoisomerase and DNA.检测细胞凋亡吞噬阶段的荧光探针:拓扑异构酶和 DNA 的酶-底物复合物。
Molecules. 2011 Jun 3;16(6):4599-614. doi: 10.3390/molecules16064599.
5
Inflammatory mechanisms in ischemic stroke: role of inflammatory cells.缺血性脑卒中的炎症机制:炎症细胞的作用。
J Leukoc Biol. 2010 May;87(5):779-89. doi: 10.1189/jlb.1109766. Epub 2010 Feb 3.
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Long-term accumulation of microglia with proneurogenic phenotype concomitant with persistent neurogenesis in adult subventricular zone after stroke.中风后成年脑室下区具有神经发生倾向表型的小胶质细胞长期积累并伴有持续的神经发生。
Glia. 2009 Jun;57(8):835-49. doi: 10.1002/glia.20810.
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Predominant phagocytic activity of resident microglia over hematogenous macrophages following transient focal cerebral ischemia: an investigation using green fluorescent protein transgenic bone marrow chimeric mice.短暂性局灶性脑缺血后,驻留小胶质细胞比血源性巨噬细胞具有更强的吞噬活性:一项使用绿色荧光蛋白转基因骨髓嵌合小鼠的研究。
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Trashing the genome: the role of nucleases during apoptosis.破坏基因组:核酸酶在细胞凋亡过程中的作用。
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9
Visualization of irreparable ischemic damage in brain by selective labeling of double strand blunt-ended DNA breaks.通过双链平端DNA断裂的选择性标记实现脑内不可修复缺血性损伤的可视化。
Mol Med. 2002 Dec;8(12):818-23.
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Two classes of DNA end-joining reactions catalyzed by vaccinia topoisomerase I.
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使用可连接荧光探针评估实验性中风中细胞死亡的吞噬清除情况。

Assessing phagocytic clearance of cell death in experimental stroke by ligatable fluorescent probes.

作者信息

Minchew Candace L, Didenko Vladimir V

机构信息

Baylor College of Medicine; Michael E. DeBakey Veterans Affairs Medical Center.

Baylor College of Medicine; Michael E. DeBakey Veterans Affairs Medical Center;

出版信息

J Vis Exp. 2014 May 27(87):51261. doi: 10.3791/51261.

DOI:10.3791/51261
PMID:24894100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4207364/
Abstract

We describe a new histochemical approach for visualization of phagocytic clearance in focal brain ischemia. The approach permits the study of elimination of dead cells in stroke by waste-management phagocytes of any cellular lineage. Although numerous cells of different origins that are capable of phagocytosis are present in ischemic brain, only part of them actively engulf and digest cell corpses. The selective visualization, quantification and analysis of such active phagocytic waste-management are helpful in assessing brain response to ischemia. Efficient cell death clearance is important for brain recovery from ischemic injury, as it opens the way for the subsequent regenerative processes. The failure to clean the corpses would result in a toxic reaction caused by non-degraded DNA and proteins. The described procedure uses fluorescent probes selectively ligated by a viral topoisomerase to characteristic DNA breaks produced in all phagocytes during engulfment and digestion of cells irreversibly damaged by ischemia. The method is a new tool for the investigation of brain reaction to ischemic injury.

摘要

我们描述了一种用于可视化局灶性脑缺血中吞噬清除作用的新组织化学方法。该方法允许研究任何细胞谱系的废物管理吞噬细胞对中风中死细胞的清除。尽管缺血性脑中存在许多不同来源的能够吞噬的细胞,但只有其中一部分会积极吞噬和消化细胞尸体。对这种活跃的吞噬废物管理进行选择性可视化、定量和分析,有助于评估大脑对缺血的反应。有效的细胞死亡清除对于大脑从缺血性损伤中恢复很重要,因为它为随后的再生过程开辟了道路。未能清理尸体会导致由未降解的DNA和蛋白质引起的毒性反应。所描述的程序使用由病毒拓扑异构酶选择性连接的荧光探针,来标记在吞噬和消化因缺血而不可逆损伤的细胞过程中,所有吞噬细胞产生的特征性DNA断裂。该方法是研究大脑对缺血性损伤反应的一种新工具。