斑马鱼
巨噬细胞
先天免疫系统
生物
转基因
炎症
吞噬作用
免疫系统
细胞生物学
基因
免疫学
体外
遗传学
作者
Felix Ellett,Luke Pase,John W. Hayman,Alex Andrianopoulos,Graham J. Lieschke
出处
期刊:Blood
[American Society of Hematology]
日期:2010-11-18
卷期号:117 (4): e49-e56
被引量:955
标识
DOI:10.1182/blood-2010-10-314120
摘要
Abstract Macrophages and neutrophils play important roles during the innate immune response, phagocytosing invading microbes and delivering antimicrobial compounds to the site of injury. Functional analyses of the cellular innate immune response in zebrafish infection/inflammation models have been aided by transgenic lines with fluorophore-marked neutrophils. However, it has not been possible to study macrophage behaviors and neutrophil/macrophage interactions in vivo directly because there has been no macrophage-only reporter line. To remove this roadblock, a macrophage-specific marker was identified (mpeg1) and its promoter used in mpeg1-driven transgenes. mpeg1-driven transgenes are expressed in macrophage-lineage cells that do not express neutrophil-marking transgenes. Using these lines, the different dynamic behaviors of neutrophils and macrophages after wounding were compared side-by-side in compound transgenics. Macrophage/neutrophil interactions, such as phagocytosis of senescent neutrophils, were readily observed in real time. These zebrafish transgenes provide a new resource that will contribute to the fields of inflammation, infection, and leukocyte biology.
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