Department of Cell and Molecular Physiology, University of North Carolina, Chapel Hill, North Carolina, USA.
Gastroenterology. 2011 Jul;141(1):197-207. doi: 10.1053/j.gastro.2011.03.042. Epub 2011 Mar 24.
BACKGROUND & AIMS: The nuclear factor κ-light-chain enhancer of activated B cells (NF-κB) transcription factor pathway is activated in response to diverse microbial stimuli to regulate expression of genes involved in immune responses and tissue homeostasis. However, the temporal and spatial activation of NF-κB in response to microbial signals have not been determined in whole living organisms, and the molecular and cellular details of these responses are not well understood. We used in vivo imaging and molecular approaches to analyze NF-κB activation in response to the commensal microbiota in transparent gnotobiotic zebrafish.
We used DNA microarrays, in situ hybridization, and quantitative reverse transcription polymerase chain reaction analyses to study the effects of the commensal microbiota on gene expression in gnotobiotic zebrafish. Zebrafish PAC2 and ZFL cells were used to study the NF-κB signaling pathway in response to bacterial stimuli. We generated transgenic zebrafish that express enhanced green fluorescent protein under transcriptional control of NF-κB, and used them to study patterns of NF-κB activation during development and microbial colonization.
Bacterial stimulation induced canonical activation of the NF-κB pathway in zebrafish cells. Colonization of germ-free transgenic zebrafish with a commensal microbiota activated NF-κB and led to up-regulation of its target genes in intestinal and extraintestinal tissues of the digestive tract. Colonization with the bacterium Pseudomonas aeruginosa was sufficient to activate NF-κB, and this activation required a functional flagellar apparatus.
In zebrafish, transcriptional activity of NF-κB is spatially and temporally regulated by specific microbial factors. The observed patterns of NF-κB-dependent responses to microbial colonization indicate that cells in the gastrointestinal tract respond robustly to the microbial environment.
核因子 κB 轻链增强子的 B 细胞(NF-κB)转录因子途径被激活,以响应各种微生物刺激,调节参与免疫反应和组织动态平衡的基因表达。然而,NF-κB 对微生物信号的时空激活尚未在整个活体生物中确定,并且这些反应的分子和细胞细节尚不清楚。我们使用体内成像和分子方法来分析透明无菌斑马鱼中对共生微生物群落的 NF-κB 激活。
我们使用 DNA 微阵列、原位杂交和定量逆转录聚合酶链反应分析来研究共生微生物群落对无菌斑马鱼基因表达的影响。斑马鱼 PAC2 和 ZFL 细胞用于研究对细菌刺激的 NF-κB 信号通路。我们生成了表达在 NF-κB 转录控制下的增强型绿色荧光蛋白的转基因斑马鱼,并用它们来研究 NF-κB 激活在发育和微生物定植过程中的模式。
细菌刺激诱导 NF-κB 途径在斑马鱼细胞中的经典激活。无菌转基因斑马鱼的共生微生物定植激活了 NF-κB,并导致其靶基因在肠道和消化道的肠外组织中上调。定植假单胞菌足以激活 NF-κB,并且这种激活需要功能齐全的鞭毛器官。
在斑马鱼中,NF-κB 的转录活性受到特定微生物因素的时空调节。对微生物定植的 NF-κB 依赖性反应的观察模式表明,胃肠道中的细胞对微生物环境有强烈的反应。