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建立一种疾病在皿中的模型来研究 SARS-CoV-2 感染在产前发育过程中的情况。

Establishing a Disease-in-a-Dish Model to Study SARS-CoV-2 Infection During Prenatal Development.

机构信息

Cell, Molecular, and Developmental Biology Graduate Program, University of California, Riverside, California.

Department of Molecular, Cell, and Systems Biology, University of California, Riverside, California.

出版信息

Curr Protoc. 2023 Apr;3(4):e759. doi: 10.1002/cpz1.759.

Abstract

Mother-to-fetus transmission of the SARS-CoV-2 virus via the placenta has been reported but cannot readily be studied in pregnant women. This protocol describes an in vitro method to investigate SARS-CoV-2 infection of human embryonic stem cells (hESCs), which are similar to epiblast cells in young postimplantation embryos. First, SARS-CoV-2 viral pseudoparticles, which contain the spike protein and a fluorescent reporter, are incorporated into a lentivirus backbone that is expanded in HEK 293T cells. Then, an infection assay based on hESCs is used with the viral pseudoparticles. An application of the infection assay in therapeutic drug screening is provided. This protocol allows infection of hESCs by SARS-CoV-2 pseudoparticles to be studied in vitro and can be used in conjunction with other assays to understand and potentially prevent infection. hESCs could also be differentiated to study infection in the three germ layers and their fetal cell derivatives. This disease-in-a-dish model could be readily applied to other hESC lines, and to other viral infections, that affect human prenatal development. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Preparing HEK 293T cells for lentiviral vector transfection Support Protocol 1: Visual inspection of transfected HEK 293T cells Basic Protocol 2: Generating viral pseudoparticles Support Protocol 2: Determining viral titer with HEK 293T-ACE2 cells Basic Protocol 3: Plating hESCs for the infection assay Support Protocol 3: Evaluating transduction efficiency.

摘要

母体向胎儿传播 SARS-CoV-2 病毒已被报道,但在孕妇中不易研究。本方案描述了一种体外方法,用于研究 SARS-CoV-2 感染人类胚胎干细胞(hESC),hESC 类似于着床后早期胚胎的外胚层细胞。首先,将含有刺突蛋白和荧光报告基因的 SARS-CoV-2 假病毒颗粒整合到慢病毒骨架中,该骨架在 HEK 293T 细胞中扩增。然后,使用基于 hESC 的感染测定法来使用这些假病毒颗粒。提供了感染测定法在治疗性药物筛选中的应用。该方案允许在体外研究 SARS-CoV-2 假病毒颗粒对 hESC 的感染,并可与其他测定法结合使用,以了解和潜在预防感染。hESC 也可以分化为研究三个胚层及其胎儿细胞衍生物中的感染。这种疾病在培养皿模型可以很容易地应用于其他 hESC 系,以及其他影响人类产前发育的病毒感染。© 2023 作者。Wiley Periodicals LLC 出版的《当代协议》。基本方案 1:为慢病毒载体转染准备 HEK 293T 细胞支持方案 1:转染 HEK 293T 细胞的目视检查基本方案 2:生成病毒假病毒颗粒支持方案 2:用 HEK 293T-ACE2 细胞确定病毒滴度基本方案 3:为感染测定法铺板 hESC 支持方案 3:评估转导效率。

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