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一种在透明斑马鱼体内追踪脂滴动态的报告基因。

An in vivo reporter for tracking lipid droplet dynamics in transparent zebrafish.

机构信息

Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, United States.

Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, United States.

出版信息

Elife. 2021 Jun 11;10:e64744. doi: 10.7554/eLife.64744.

Abstract

Lipid droplets are lipid storage organelles found in nearly all cell types from adipocytes to cancer cells. Although increasingly implicated in disease, current methods to study lipid droplets in vertebrate models rely on static imaging or the use of fluorescent dyes, limiting investigation of their rapid in vivo dynamics. To address this, we created a lipid droplet transgenic reporter in whole animals and cell culture by fusing tdTOMATO to Perilipin-2 (PLIN2), a lipid droplet structural protein. Expression of this transgene in transparent zebrafish enabled in vivo imaging of adipose depots responsive to nutrient deprivation and high-fat diet. Simultaneously, we performed a large-scale in vitro chemical screen of 1280 compounds and identified several novel regulators of lipolysis in adipocytes. Using our zebrafish line, we validated several of these novel regulators and revealed an unexpected role for nitric oxide in modulating adipocyte lipid droplets. Similarly, we expressed the PLIN2-tdTOMATO transgene in melanoma cells and found that the nitric oxide pathway also regulated lipid droplets in cancer. This model offers a tractable imaging platform to study lipid droplets across cell types and disease contexts using chemical, dietary, or genetic perturbations.

摘要

脂滴是几乎存在于所有细胞类型(从脂肪细胞到癌细胞)中的脂质储存细胞器。尽管越来越多的疾病与脂滴有关,但目前在脊椎动物模型中研究脂滴的方法依赖于静态成像或荧光染料的使用,限制了对其快速体内动力学的研究。为了解决这个问题,我们通过将 tdTOMATO 融合到脂滴结构蛋白 Perilipin-2(PLIN2)中,在整个动物和细胞培养物中创建了一种脂滴转基因报告器。在透明的斑马鱼中表达这种转基因,能够对响应营养剥夺和高脂肪饮食的脂肪组织进行体内成像。同时,我们对 1280 种化合物进行了大规模的体外化学筛选,并在脂肪细胞中鉴定出几种新的脂肪分解调节剂。使用我们的斑马鱼系,我们验证了其中的几种新型调节剂,并揭示了一氧化氮在调节脂肪细胞脂滴中的意外作用。同样,我们在黑色素瘤细胞中表达了 PLIN2-tdTOMATO 转基因,发现一氧化氮通路也调节了癌症中的脂滴。该模型提供了一种可行的成像平台,可用于使用化学、饮食或遗传干扰来研究跨细胞类型和疾病背景的脂滴。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/867d/8195600/040c9b19f464/elife-64744-fig1.jpg

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