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热休克通过SAPK/JNK和HSF1途径对OCT4进行负调控,从而指导人胚胎干细胞退出自我更新程序。

Heat shock instructs hESCs to exit from the self-renewal program through negative regulation of OCT4 by SAPK/JNK and HSF1 pathway.

作者信息

Byun Kyunghee, Kim Taek-Kyun, Oh Jeehyun, Bayarsaikhan Enkhjargal, Kim Daesik, Lee Min Young, Pack Chan-Gi, Hwang Daehee, Lee Bonghee

机构信息

Center for Genomics and Proteomics & Stem Cell Core Facility, Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Incheon 406-840, Republic of Korea; Department of Anatomy and Cell Biology, Gachon University Medical School, Incheon 406-840, Republic of Korea.

出版信息

Stem Cell Res. 2013 Nov;11(3):1323-34. doi: 10.1016/j.scr.2013.08.014. Epub 2013 Sep 8.

Abstract

Environmental factors affect self-renewal of stem cells by modulating the components of self-renewal networks. Heat shock, an environmental factor, induces heat shock factors (HSFs), which up-regulate stress response-related genes. However, the link of heat shock to self-renewal of stem cells has not been elucidated yet. Here, we present the direct link of heat shock to a core stem cell regulator, OCT4, in the self-renewal network through SAPK/JNK and HSF1 pathway. We first showed that heat shock initiated differentiation of human embryonic stem cells (hESCs). Gene expression analysis revealed that heat shock increased the expression of many genes involved in cellular processes related to differentiation of stem cells. We then examined the effects of HSFs induced by heat shock on core self-renewal factors. Among HSFs, heat shock induced mainly HSF1 in hESCs. The HSF1 repressed the expression of OCT4, leading to the differentiation of hESCs and the above differentiation-related gene expression change. We further examined the effects of the upstream MAP (mitogen-activated protein) kinases of HSF1 on the repression of OCT4 expression by HSF1. Among the MAP kinases, SAPK/JNK controlled predominantly the repression of the OCT4 expression by HSF1. The direct link of heat shock to the core self-renewal regulator through SAPK/JNK and HSF1 provides a fundamental basis for understanding the effect of heat and other stresses involving activation of HSF1 on the self-renewal program and further controlling differentiation of hESCs in a broad spectrum of stem cell applications using these stresses.

摘要

环境因素通过调节自我更新网络的组成部分来影响干细胞的自我更新。热休克作为一种环境因素,可诱导热休克因子(HSFs),从而上调应激反应相关基因。然而,热休克与干细胞自我更新之间的联系尚未阐明。在此,我们通过SAPK/JNK和HSF1途径,揭示了热休克与自我更新网络中核心干细胞调节因子OCT4之间的直接联系。我们首先发现热休克引发了人类胚胎干细胞(hESCs)的分化。基因表达分析表明,热休克增加了许多与干细胞分化相关细胞过程的基因表达。然后,我们研究了热休克诱导的HSFs对核心自我更新因子的影响。在HSFs中,热休克在hESCs中主要诱导HSF1。HSF1抑制OCT4的表达,导致hESCs分化以及上述与分化相关的基因表达变化。我们进一步研究了HSF1的上游丝裂原活化蛋白(MAP)激酶对HSF1抑制OCT4表达的影响。在MAP激酶中,SAPK/JNK主要控制HSF1对OCT4表达的抑制。热休克通过SAPK/JNK和HSF1与核心自我更新调节因子的直接联系,为理解热和其他涉及HSF1激活的应激对自我更新程序的影响,以及在广泛的干细胞应用中利用这些应激进一步控制hESCs的分化提供了基础。

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