Suppr超能文献

使用微聚集装置轻松高效地生产完全胚胎干细胞来源的小鼠。

Easy and efficient production of completely embryonic-stem-cell-derived mice using a micro-aggregation device.

机构信息

Laboratory for Mouse Genetic Engineering, RIKEN Center for Biosystems Dynamics Research, 1-3 Yamadaoka, Suita, Osaka, Japan.

Laboratory for Synthetic Biology, RIKEN Center for Biosystems Dynamics Research, 1-3 Yamadaoka, Suita, Osaka, Japan.

出版信息

PLoS One. 2018 Sep 19;13(9):e0203056. doi: 10.1371/journal.pone.0203056. eCollection 2018.

Abstract

There is an increasing demand for genetically modified mice produced without crossing, for rapid phenotypic screening studies at the organismal level. For this purpose, generation of completely embryonic-stem-cell (ESC)-derived chimeric mice without crossing is now possible using a microinjection or aggregation method with 3i culture medium. However, the microinjection of ESCs into blastocyst, morula, or 8-cell-stage embryos requires a highly skilled operator. The aggregation method is an easier alternative, but the conventional aggregation protocol still requires special skills. To make the aggregation method easier and more precise, here we developed a micro-aggregation device. Unlike conventional 3-dimensional culture, which uses hanging-drop devices for aggregation, we fabricated a polystyrene funnel-like structure to smoothly drop ESCs into a small area (300-μm in diameter) at the bottom of the device. The bottom area was designed so that the surface tension of the liquid-air interface prevents the cells from falling. After aggregation, the cells can be recovered by simply exerting pressure on the liquid from the top. The microdevice can be set upon a regular 96-well plate, so it is compatible with multichannel pipette use or machine operation. Using the microdevice, we successfully obtained chimeric blastocysts, which when transplanted resulted in completely ESC-derived chimeric mice with high efficiency. By changing the number of ESCs in the aggregate, we found that the optimum number of co-cultured ESCs was around 90~120 per embryo. Under this condition, the efficiency of generating completely ESC-derived mice was the same or better than that of the injection method. These results indicated that our microdevice can be used to produce completely ESC-derived chimeric mice easily and with a high success rate, and thus represents a promising alternative to the conventional microinjection or aggregation method, especially for high-throughput, parallel experimental applications.

摘要

人们对无需交配即可生产的基因修饰小鼠的需求日益增长,以便在机体水平上进行快速表型筛选研究。为此,现在可以使用微注射或 3i 培养基聚集方法,无需交配即可生成完全源自胚胎干细胞(ESC)的嵌合小鼠。然而,将 ESC 微注射到囊胚、桑椹胚或 8 细胞期胚胎中需要高度熟练的操作人员。聚集方法是一种更简单的替代方法,但传统的聚集方案仍然需要特殊技能。为了使聚集方法更容易且更精确,我们在这里开发了一种微聚集装置。与使用悬滴设备进行聚集的传统 3 维培养不同,我们制造了一个聚苯乙烯漏斗状结构,可将 ESC 平稳地滴入装置底部的一个小区域(直径 300μm)。底部区域的设计使得液体-空气界面的表面张力阻止细胞掉落。聚集后,只需从顶部对液体施加压力即可回收细胞。微装置可设置在常规的 96 孔板上,因此兼容多通道移液器使用或机器操作。使用微装置,我们成功获得了嵌合囊胚,当将其移植时,可得到完全源自 ESC 的嵌合小鼠,效率很高。通过改变聚集物中的 ESC 数量,我们发现最佳共培养 ESC 数量约为每个胚胎 90~120 个。在这种条件下,生成完全源自 ESC 的小鼠的效率与注射方法相同或更好。这些结果表明,我们的微装置可用于轻松且高成功率地生成完全源自 ESC 的嵌合小鼠,因此代表了对传统微注射或聚集方法的有前途的替代方法,尤其是对于高通量、并行实验应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfa0/6145547/5f34bf57ac2f/pone.0203056.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验