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一种高效、易用的人类胚胎干细胞和诱导多能干细胞的冻存方案。

An efficient and easy-to-use cryopreservation protocol for human ES and iPS cells.

机构信息

Department of Stem Cells and Developmental Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

出版信息

Nat Protoc. 2010 Mar;5(3):588-94. doi: 10.1038/nprot.2009.247. Epub 2010 Mar 4.

Abstract

Here we describe a simple and efficient human embryonic stem (ES) and induced pluripotent stem (iPS) cells cryopreservation protocol. This protocol involves the use of Rho-associated kinase (ROCK) inhibitor, Y-27632, for the feeder-free dissociated cells. The addition of ROCK inhibitor to both pre- and post-thaw culture media enhanced the cloning efficiency. The presence of Y-27632 in Matrigel further increased the cloning efficiency. As compared with other available protocols for human ES and iPS cells cryopreservation, our protocol differs in the technical simplicity, high cloning efficiency and post-thawing passaging. We believe that this protocol could be a generally applicable and robust platform for feeder-free cryopreservation and the expansion of present and future applications of human ES and iPS cells. The treatment with ROCK inhibitor, cell harvesting and the freezing-thawing process usually takes about 2 h excluding overnight incubation at -80 degrees C.

摘要

在这里,我们描述了一种简单高效的人类胚胎干细胞(ES)和诱导多能干细胞(iPS)细胞的冷冻保存方案。该方案涉及使用 Rho 相关激酶(ROCK)抑制剂 Y-27632 对无饲养层分离细胞进行处理。在预冻和冻后培养基中添加 ROCK 抑制剂可提高克隆效率。Matrigel 中存在 Y-27632 可进一步提高克隆效率。与其他现有的人类 ES 和 iPS 细胞冷冻保存方案相比,我们的方案在技术简单性、高克隆效率和冻后传代方面有所不同。我们相信,该方案可为无饲养层冷冻保存以及目前和未来的人类 ES 和 iPS 细胞应用提供一个普遍适用且稳健的平台。ROCK 抑制剂处理、细胞收获和冻融过程通常需要大约 2 小时,不包括在-80°C 下过夜孵育。

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