Summary

使用免疫荧光检测斑马鱼胚胎心脏PM2.5诱发DNA损伤

Published: February 15, 2021
doi:

Summary

该协议使用免疫荧光检测检测斑马鱼胚胎解剖心脏中PM2.5诱发的DNA损伤。

Abstract

环境细颗粒物(PM2.5)暴露可导致心脏发育毒性,但潜在的分子机制尚不清楚。8-羟基-2’脱氧酶(8-OHdG)是氧化DNA损伤的标记,+H2AX是DNA双链断裂的敏感标记。在这项研究中,我们旨在通过免疫荧光检测斑马鱼胚胎心脏的PM2.5诱导8-OHDG和+H2AX变化。斑马鱼胚胎在受精后2小时(hpf)2小时时,以5微克/mL的PM2.5 处理可提取的有机物质(EOM)。DMSO 被用作车辆控制。在72马力,心脏被解剖从胚胎使用注射器针和固定和渗透。被阻塞后,用原样抗体对8-OHdG和+H2AX进行探测。然后用二次抗体清洗和孵育样品。由此产生的图像在荧光显微镜下观察,并使用 ImageJ 进行量化。结果表明,EOM从下午2.5 显著增强8-OHDG和+H2AX信号在斑马鱼胚胎的心脏。然而,NAC作为活性氧物种(ROS)的清除剂,部分抵消了EOM引起的DNA损伤。在这里,我们提出了一个免疫荧光方案,用于研究DNA损伤在PM2.5诱发的心脏缺陷中的作用,可用于检测斑马鱼胚胎心脏中环境化学诱发的蛋白质表达变化。

Introduction

空气污染是目前世界面临的一个严重的环境问题。环境细颗粒物(PM2.5)是空气质量最重要的指标之一,可携带大量有害物质进入血液循环系统,对人体健康造成严重危害。流行病学研究表明,PM2.5暴露可导致先天性心脏缺陷(CHDs)2,3的风险增加。动物实验的证据表明,PM2.5可导致斑马鱼胚胎和小鼠后代心脏发育异常,但PM2.5心脏发育毒性的分子机制仍鲜为人知

DNA损伤可引起细胞周期骤停并诱发凋亡,从而可能广泛破坏祖细胞的潜力,进而损害心脏发育有充分证据表明,环境污染物,包括PM2.5,有可能通过氧化应激机制8,9攻击DNA。人类和斑马鱼心脏发育都对氧化应激10、11、12敏感。8-OHdG 是一种氧化性 DNA 损伤标记,+H2AX 信号是 DNA 双链断裂的标志。N-乙酰-L-半胱氨酸(NAC)是细胞内半胱氨酸和谷胱甘肽的合成前体,被广泛用作抗氧化化合物。在这项研究中,我们使用NAC来研究氧化应激在下午2.5诱发DNA损伤13中的作用。

斑马鱼作为脊椎动物的模型,已被广泛用于研究心脏发育和人类心血管疾病,因为心脏发育机制在脊椎动物保存高度。使用斑马鱼作为模型的优势包括它们体积小、繁殖能力强和饲养成本低。这些研究特别感兴趣的是,斑马鱼胚胎在早期发育过程中不依赖于循环系统,并且能够存活下来,严重心脏畸形14。此外,它们的透明度允许在显微镜下直接观察整个身体。因此,斑马鱼胚胎提供了一个绝佳的机会,以评估参与诱导心脏发育毒性的分子机制,由于接触各种环境化学品5,16,17。我们之前曾报道,PM2.5引起的氧化应激导致DNA损伤和凋亡,导致斑马鱼18的心脏畸形。在这项研究中,我们提供了一个详细的协议,用于调查PM2.5引起的斑马鱼胚胎心脏DNA损伤。

Protocol

本研究中使用的野生斑马鱼(AB)是从中国武汉国家斑马鱼资源中心获得的。这里概述的所有动物程序都经过了苏乔大学伦理委员会动物护理研究所的审查和批准。 1. 下午2.5 采样和有机化合物提取 注:下午2.5 收集于中国苏州市区,2015年8月1-7日,如前5日所述。 在 500 °C 消声炉中烘烤 47 mm 石英膜过滤器 2 小时,?…

Representative Results

这种免疫荧光检测是测量暴露于环境化学物质的斑马鱼胚胎心脏蛋白质表达变化的一种敏感而具体的方法。 在这个具有代表性的分析中,在没有抗氧化剂NAC的情况下暴露于PM2.5的胚胎被评估为存在心脏畸形(图1)。观察到,与 DMSO 控制治疗的心脏相比,PM2.5导致心脏畸形发生显著增加,?…

Discussion

虽然斑马鱼是研究环境化学物质心脏发育毒性的极好的脊椎动物模型,但由于胚胎心脏体积小,很难获得足够的蛋白质进行西方污点分析。因此,我们提出了一种敏感的免疫荧光方法,用于量化暴露在PM2.5下的斑马鱼胚胎心脏中DNA损伤生物标志物的蛋白质表达水平。

在解剖过程中,保持心脏的完整性是很重要的。根据我们的经验,在 72 hpf 下执行隔离相对容易。此外?…

Divulgazioni

The authors have nothing to disclose.

Acknowledgements

这项工作得到了中国自然科学基金会(资助编号:81870239、81741005、81972999)和江苏省高等学校优先学术项目发展的支持。

Materials

8-OHdG Antibody Santa Cruz Biotechnology, USA sc-66036 Primary antibody
Analytical balance Sartorius,China BSA124S
BSA Solarbio,Beijing,China SW3015 For blocking
DAPI Abcam, USA ab104139 For nuclear counterstain.
DMSO Solarbio,Beijing,China D8371
Fluorescence microscope Olympus, Japan IX73 For imaging fluorescence signals/
Goat Anti-Rabbit IgG Cy3 Carlsbad,USA CW0159 Secondary antibody
Goat Anti-Rabbit IgG FITC Carlsbad,USA RS0003 Secondary antibody
N-Acetyl-L-cysteine(NAC) Adamas-Beta, Shanghai, China 616-91-1
Orbital shaker QILINBEIER,China TS-1
Paraformaldehyde Sigma,China P6148 Make 4% paraformaldehyde for fixation.
Phosphate Buffered Saline HyClone,USA SH30256.01 Prepare 0.1% Tween in PBS for washing.
PM2.5 sampler TianHong,Wuhan, China TH-150C For 24-hr uninterrupted PM2.5 sampling.
Re-circulating aquaculture system HaiSheng,Shanghai,China The zebrafish was maintained in it.
Soxhlet extractor ZhengQiao,Shanghai, China BSXT-02 For organic components extraction.
Stereomicroscope Nikon,Canada SMZ645 For heart dissection from zebrafish embryos.
Tricaine methanesulfonate (MS222) Sigma,China E10521 To anesthetize zebrafish embryos
Tween 20 Sigma,China P1379
γH2AX Antibody Abcam, USA ab26350 Primary antibody

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Citazione di questo articolo
Huang, Y., Tao, Y., Cai, C., Chen, J., Ji, C., Aniagu, S., Jiang, Y., Chen, T. Using Immunofluorescence to Detect PM2.5-induced DNA Damage in Zebrafish Embryo Hearts. J. Vis. Exp. (168), e62021, doi:10.3791/62021 (2021).

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