下载PDF
{"title":"Generation of ERK-Independent Human and Non-Human Primate Pluripotent Stem Cells","authors":"Alejandro De Los Angeles","doi":"10.1002/cpsc.85","DOIUrl":null,"url":null,"abstract":"<p>The production of human organs inside human-animal interspecies chimeras might one day comprise a viable strategy for generating patient-specific organs, but such experiments will require human chimera-competent pluripotent stem (PS) cells. The stabilization of PS cell self-renewal in serum-free medium and ERK blockade might be critical for capturing primate chimera-competent pluripotency. It has recently been shown that shielding primate cells from the activation of ERK, WNT, and PKC signaling is crucial for deriving African green monkey ERK-independent PS cells. Here, I show that this principle is generalizable to human cells. In this chapter, methods are provided to reset conventional human PS cells to ERK-independence using histone deacetylase inhibitors and PGCX media comprised of N2B27 medium supplemented with LIF, PD0325901, Go6983, CHIR99021, and XAV939. The novel stem cells exhibit higher levels of KLF4 and manifest increased mitochondrial membrane depolarization. However, the author observed that not all PS cell lines are amenable to small molecule-mediated resetting. The ERK-independent PS cells described herein will provide a useful resource for testing interspecies organogenesis strategies. © 2019 by John Wiley & Sons, Inc.</p>","PeriodicalId":53703,"journal":{"name":"Current Protocols in Stem Cell Biology","volume":"49 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpsc.85","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Stem Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpsc.85","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 2
引用
批量引用
Abstract
The production of human organs inside human-animal interspecies chimeras might one day comprise a viable strategy for generating patient-specific organs, but such experiments will require human chimera-competent pluripotent stem (PS) cells. The stabilization of PS cell self-renewal in serum-free medium and ERK blockade might be critical for capturing primate chimera-competent pluripotency. It has recently been shown that shielding primate cells from the activation of ERK, WNT, and PKC signaling is crucial for deriving African green monkey ERK-independent PS cells. Here, I show that this principle is generalizable to human cells. In this chapter, methods are provided to reset conventional human PS cells to ERK-independence using histone deacetylase inhibitors and PGCX media comprised of N2B27 medium supplemented with LIF, PD0325901, Go6983, CHIR99021, and XAV939. The novel stem cells exhibit higher levels of KLF4 and manifest increased mitochondrial membrane depolarization. However, the author observed that not all PS cell lines are amenable to small molecule-mediated resetting. The ERK-independent PS cells described herein will provide a useful resource for testing interspecies organogenesis strategies. © 2019 by John Wiley & Sons, Inc.
不依赖erk的人类和非人类灵长类多能干细胞的产生
在人-动物种间嵌合体中生产人体器官可能有一天会成为一种产生患者特异性器官的可行策略,但这样的实验将需要人类嵌合体多能干细胞(PS)。无血清培养基中PS细胞自我更新的稳定和ERK阻断可能是获得灵长类嵌合体多能性的关键。最近有研究表明,屏蔽灵长类细胞免受ERK、WNT和PKC信号的激活对于获得非洲绿猴ERK不依赖性PS细胞至关重要。在这里,我展示了这个原理可以推广到人类细胞。本章提供了使用组蛋白去乙酰化酶抑制剂和PGCX培养基(由N2B27培养基补充LIF、PD0325901、Go6983、CHIR99021和XAV939组成)将常规人PS细胞重置为erk独立性的方法。这种新型干细胞表现出更高水平的KLF4,并表现出线粒体膜去极化的增加。然而,作者观察到并非所有的PS细胞系都适合小分子介导的重置。本文描述的不依赖erk的PS细胞将为测试种间器官发生策略提供有用的资源。©2019 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。