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GSK3 和 MEK 抑制对胚胎干细胞中 Nanog 异质性的诱导和选择性作用。

Inductive and Selective Effects of GSK3 and MEK Inhibition on Nanog Heterogeneity in Embryonic Stem Cells.

机构信息

Department of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland; Research Unit Stem Cell Dynamics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.

Department of Biosystems Science and Engineering, ETH Zurich, 4058 Basel, Switzerland.

出版信息

Stem Cell Reports. 2018 Jul 10;11(1):58-69. doi: 10.1016/j.stemcr.2018.04.019. Epub 2018 May 17.

Abstract

Embryonic stem cells (ESCs) display heterogeneous expression of pluripotency factors such as Nanog when cultured with serum and leukemia inhibitory factor (LIF). In contrast, dual inhibition of the signaling kinases GSK3 and MEK (2i) converts ESC cultures into a state with more uniform and high Nanog expression. However, it is so far unclear whether 2i acts through an inductive or selective mechanism. Here, we use continuous time-lapse imaging to quantify the dynamics of death, proliferation, and Nanog expression in mouse ESCs after 2i addition. We show that 2i has a dual effect: it both leads to increased cell death of Nanog low ESCs (selective effect) and induces and maintains high Nanog levels (inductive effect) in single ESCs. Genetic manipulation further showed that presence of NANOG protein is important for cell viability in 2i medium. This demonstrates complex Nanog-dependent effects of 2i treatment on ESC cultures.

摘要

胚胎干细胞(ESCs)在含有血清和白血病抑制因子(LIF)的条件下培养时,会呈现出多能性因子如 Nanog 的异质性表达。相比之下,双重抑制信号激酶 GSK3 和 MEK(2i)可将 ESC 培养物转化为具有更均匀和高 Nanog 表达的状态。然而,到目前为止,尚不清楚 2i 是否通过诱导或选择性机制起作用。在这里,我们使用连续时间 lapse 成像技术来定量分析添加 2i 后小鼠 ESCs 中死亡、增殖和 Nanog 表达的动力学。我们表明 2i 具有双重作用:它既导致 Nanog 低表达的 ESCs 死亡增加(选择性作用),又诱导并维持单个 ESCs 中高 Nanog 水平(诱导作用)。遗传操作进一步表明,NANOG 蛋白的存在对于 2i 培养基中的细胞活力很重要。这表明 2i 处理对 ESC 培养物具有复杂的 Nanog 依赖性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e31f/6066909/b8cb93c7e5fb/fx1.jpg

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