Kondo Masayo, Sugimoto Michihiko, Abe Kuniya
Technology and Development Team for Mammalian Genome Dynamics, RIKEN BioResource Research Center, Tsukuba, Ibaraki, Japan.
Division of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan.
Curr Protoc Stem Cell Biol. 2018 Aug;46(1):e60. doi: 10.1002/cpsc.60. Epub 2018 Jul 13.
Epiblast stem cells (EpiSCs) are primed pluripotent stem cells (PSCs) derived from mouse postimplantation embryos. Interestingly, EpiSCs share many characteristics with human PSCs such as human embryonic stem cells (hESCs) and human induced PSCs (hiPSC). Thus, EpiSCs can serve as a model for studying primed states of pluripotency. This article describes a simple yet highly efficient protocol for EpiSC derivation and maintenance of homogenous EpiSCs using an inhibitor of WNT secretion. Using this method, EpiSCs can be readily derived from mouse strains with different genetic background including C57BL/6N. The EpiSCs derived by this protocol maintain a homogenous, undifferentiated status, yet retain high differentiation potential. Unlike EpiSCs established by the original protocol, the new EpiSC lines require the continued presence of WNT inhibitor, suggesting intrinsic differences from EpiSCs made by the original method. This new version of EpiSCs will provide clues to understand the nature of primed states of mammalian pluripotent cells and may facilitate establishment of a better protocol for directed differentiation from the primed state. © 2018 by John Wiley & Sons, Inc.
上胚层干细胞(EpiSCs)是源自小鼠植入后胚胎的始发态多能干细胞(PSCs)。有趣的是,EpiSCs与人类PSCs具有许多共同特征,如人类胚胎干细胞(hESCs)和人类诱导多能干细胞(hiPSC)。因此,EpiSCs可作为研究多能性始发态的模型。本文描述了一种简单而高效的方案,用于使用WNT分泌抑制剂来衍生EpiSCs并维持其同质状态。使用这种方法,可以很容易地从包括C57BL / 6N在内的具有不同遗传背景的小鼠品系中获得EpiSCs。通过该方案获得的EpiSCs保持同质的未分化状态,但保留高分化潜能。与通过原始方案建立的EpiSCs不同,新的EpiSC系需要持续存在WNT抑制剂,这表明其与原始方法获得的EpiSCs存在内在差异。这种新版本的EpiSCs将为理解哺乳动物多能细胞始发态的本质提供线索,并可能有助于建立从始发态进行定向分化的更好方案。©2018约翰威立父子公司。