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通过将多能干细胞与胚胎聚集来制备小鼠嵌合体。

Production of mouse chimeras by aggregating pluripotent stem cells with embryos.

作者信息

Nagy Andras, Nagy Kristina, Gertsenstein Marina

机构信息

Mount Sinai Hospital, Samuel Lunenfeld Research Institute,Toronto, Ontario, Canada.

出版信息

Methods Enzymol. 2010;476:123-49. doi: 10.1016/S0076-6879(10)76008-0.

Abstract

Experimental mouse chimeras have served as immensely important research tools for studying many aspects of mammalian development ever since they first were produced over 50 years ago. Chimera studies have served as crucial assays in the era of modern mouse genetics that was triggered by the advent of mouse embryonic stem cells. Lately, chimeras are also used as proof of pluripotency and normality of induced pluripotent stem cells. With this long history in mind, it may seem surprising that chimeras now have an ever-increasing role to play. The high-throughput mouse gene targeting projects are in the process of producing ES cell lines with a mutation in each of the close to 20,000 known protein coding genes. These will all be waiting for germline transmission through chimeras. Such a large-scale approach calls for simplified methods for generating germline transmitting chimeras. In this chapter, we will describe the currently most cost efficient and simple method; the aggregation of pluripotent stem cells with diploid or tetraploid mouse embryos. Since most of the large knockout projects are using the C57BL/6 background, we will pay special attention to cell lines derived from this inbred strain.

摘要

自从50多年前首次培育出实验性小鼠嵌合体以来,它们一直是研究哺乳动物发育诸多方面的极为重要的研究工具。在由小鼠胚胎干细胞的出现所引发的现代小鼠遗传学时代,嵌合体研究一直是关键的分析方法。最近,嵌合体还被用作诱导多能干细胞多能性和正常性的证据。鉴于其悠久的历史,嵌合体如今发挥着越来越重要的作用这一点可能看起来令人惊讶。高通量小鼠基因打靶项目正在生产近20000个已知蛋白质编码基因中每个基因都发生突变的胚胎干细胞系。所有这些都将等待通过嵌合体进行种系传递。这种大规模方法需要简化的生成种系传递嵌合体的方法。在本章中,我们将描述目前最具成本效益且简单的方法;将多能干细胞与二倍体或四倍体小鼠胚胎聚集。由于大多数大型基因敲除项目都使用C57BL/6背景,我们将特别关注源自该近交系的细胞系。

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