Walton Eric M, Cronan Mark R, Beerman Rebecca W, Tobin David M
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America; Center for Host-Microbial Interactions, Duke University Medical Center, Durham, North Carolina, United States of America.
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America; Department of Immunology, Duke University Medical Center, Durham, North Carolina, United States of America; Center for Host-Microbial Interactions, Duke University Medical Center, Durham, North Carolina, United States of America.
PLoS One. 2015 Oct 7;10(10):e0138949. doi: 10.1371/journal.pone.0138949. eCollection 2015.
Transgenic labeling of innate immune cell lineages within the larval zebrafish allows for real-time, in vivo analyses of microbial pathogenesis within a vertebrate host. To date, labeling of zebrafish macrophages has been relatively limited, with the most specific expression coming from the mpeg1 promoter. However, mpeg1 transcription at both endogenous and transgenic loci becomes attenuated in the presence of intracellular pathogens, including Salmonella typhimurium and Mycobacterium marinum. Here, we describe mfap4 as a macrophage-specific promoter capable of producing transgenic lines in which transgene expression within larval macrophages remains stable throughout several days of infection. Additionally, we have developed a novel macrophage-specific Cre transgenic line under the control of mfap4, enabling macrophage-specific expression using existing floxed transgenic lines. These tools enrich the repertoire of transgenic lines and promoters available for studying zebrafish macrophage dynamics during infection and inflammation and add flexibility to the design of future macrophage-specific transgenic lines.
对斑马鱼幼体体内先天性免疫细胞谱系进行转基因标记,有助于在脊椎动物宿主内对微生物致病机制进行实时、活体分析。迄今为止,斑马鱼巨噬细胞的标记相对有限,最具特异性的表达来自mpeg1启动子。然而,在包括鼠伤寒沙门氏菌和海分枝杆菌在内的细胞内病原体存在的情况下,内源性和转基因位点的mpeg1转录都会减弱。在此,我们将mfap4描述为一种巨噬细胞特异性启动子,它能够产生转基因品系,其中幼体巨噬细胞内的转基因表达在感染的数天内保持稳定。此外,我们还开发了一种在mfap4控制下的新型巨噬细胞特异性Cre转基因品系,可利用现有的loxP侧翼转基因品系实现巨噬细胞特异性表达。这些工具丰富了可用于研究感染和炎症过程中斑马鱼巨噬细胞动态的转基因品系和启动子库,并为未来巨噬细胞特异性转基因品系的设计增加了灵活性。