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斑马鱼作为载脂蛋白生物学的模型:综合表达分析及载脂蛋白A-IV在调节食物摄入中的作用

Zebrafish as a model for apolipoprotein biology: comprehensive expression analysis and a role for ApoA-IV in regulating food intake.

作者信息

Otis Jessica P, Zeituni Erin M, Thierer James H, Anderson Jennifer L, Brown Alexandria C, Boehm Erica D, Cerchione Derek M, Ceasrine Alexis M, Avraham-Davidi Inbal, Tempelhof Hanoch, Yaniv Karina, Farber Steven A

机构信息

Carnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA.

Carnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA.

出版信息

Dis Model Mech. 2015 Mar;8(3):295-309. doi: 10.1242/dmm.018754. Epub 2015 Jan 29.

Abstract

Improved understanding of lipoproteins, particles that transport lipids throughout the circulation, is vital to developing new treatments for the dyslipidemias associated with metabolic syndrome. Apolipoproteins are a key component of lipoproteins. Apolipoproteins are proteins that structure lipoproteins and regulate lipid metabolism through control of cellular lipid exchange. Constraints of cell culture and mouse models mean that there is a need for a complementary model that can replicate the complex in vivo milieu that regulates apolipoprotein and lipoprotein biology. Here, we further establish the utility of the genetically tractable and optically clear larval zebrafish as a model of apolipoprotein biology. Gene ancestry analyses were implemented to determine the closest human orthologs of the zebrafish apolipoprotein A-I (apoA-I), apoB, apoE and apoA-IV genes and therefore ensure that they have been correctly named. Their expression patterns throughout development were also analyzed, by whole-mount mRNA in situ hybridization (ISH). The ISH results emphasized the importance of apolipoproteins in transporting yolk and dietary lipids: mRNA expression of all apolipoproteins was observed in the yolk syncytial layer, and intestinal and liver expression was observed from 4-6 days post-fertilization (dpf). Furthermore, real-time PCR confirmed that transcription of three of the four zebrafish apoA-IV genes was increased 4 hours after the onset of a 1-hour high-fat feed. Therefore, we tested the hypothesis that zebrafish ApoA-IV performs a conserved role to that in rat in the regulation of food intake by transiently overexpressing ApoA-IVb.1 in transgenic larvae and quantifying ingestion of co-fed fluorescently labeled fatty acid during a high-fat meal as an indicator of food intake. Indeed, ApoA-IVb.1 overexpression decreased food intake by approximately one-third. This study comprehensively describes the expression and function of eleven zebrafish apolipoproteins and serves as a springboard for future investigations to elucidate their roles in development and disease in the larval zebrafish model.

摘要

更好地理解脂蛋白(即在整个循环系统中运输脂质的颗粒)对于开发治疗与代谢综合征相关的血脂异常的新疗法至关重要。载脂蛋白是脂蛋白的关键组成部分。载脂蛋白是构成脂蛋白并通过控制细胞脂质交换来调节脂质代谢的蛋白质。细胞培养和小鼠模型的局限性意味着需要一种互补模型,该模型能够复制调节载脂蛋白和脂蛋白生物学的复杂体内环境。在此,我们进一步确立了基因易操作且光学透明的斑马鱼幼体作为载脂蛋白生物学模型的实用性。进行了基因谱系分析,以确定斑马鱼载脂蛋白A-I(apoA-I)、apoB、apoE和apoA-IV基因最接近的人类直系同源基因,从而确保它们被正确命名。还通过全胚胎mRNA原位杂交(ISH)分析了它们在整个发育过程中的表达模式。ISH结果强调了载脂蛋白在运输卵黄和膳食脂质中的重要性:在卵黄合胞体层中观察到所有载脂蛋白的mRNA表达,并且在受精后4-6天(dpf)观察到肠道和肝脏表达。此外,实时PCR证实,在1小时高脂饲料投喂开始后4小时,四个斑马鱼apoA-IV基因中的三个的转录增加。因此,我们通过在转基因幼体中瞬时过表达ApoA-IVb.1并在高脂餐期间定量共投喂的荧光标记脂肪酸的摄取作为食物摄入的指标,来检验斑马鱼ApoA-IV在调节食物摄入方面与大鼠具有保守作用的假设。确实,ApoA-IVb.1过表达使食物摄入量减少了约三分之一。这项研究全面描述了11种斑马鱼载脂蛋白的表达和功能,并为未来阐明它们在斑马鱼幼体模型的发育和疾病中的作用的研究提供了一个跳板。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b306/4348566/fe5396a7663e/DMM018754F1.jpg

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