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CHIR99021通过调节细胞铁代谢维持细胞干性

CHIR99021 Maintenance of the Cell Stemness by Regulating Cellular Iron Metabolism.

作者信息

Han Yingying, He Yong, Jin Xiaofang, Xie Jiayi, Yu Peng, Gao Guofen, Chang Shiyang, Zhang Jianhua, Chang Yan-Zhong

机构信息

Laboratory of Molecular Iron Metabolism, Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology of Hebei Province, Ministry of Education Key Laboratory of Molecular and Cellular Biology, College of Life Science, Hebei Normal University, Shijiazhuang 050024, China.

College of Basic Medical Sciences, Hebei Medical University, Shijiazhuang 050017, China.

出版信息

Antioxidants (Basel). 2023 Feb 4;12(2):377. doi: 10.3390/antiox12020377.

Abstract

CHIR99021 is an aminopyrimidine derivative, which can efficiently inhibit the activity of glycogen synthesis kinase 3α (GSK-3α) and GSK-3β. As an essential component of stem cell culture medium, it plays an important role in maintaining cell stemness. However, the mechanism of its role is not fully understood. In the present study, we first found that removal of CHIR99021 from embryonic stem cell culture medium reduced iron storage in mouse embryonic stem cells (mESCs). CHIR99021-treated Neuro-2a cells led to an upregulation of ferritin expression and an increase in intracellular iron levels, along with GSK3β inhibition and Wnt/GSK-3β/β-catenin pathway activation. In addition, iron treatment activated the classical Wnt pathway by affecting the expression of β-catenin in the Neuro-2a cells. Our data link the role of iron in the maintenance of cell stemness via the Wnt/GSK-3β/β-catenin signaling pathway, and identify intermediate molecules, including Steap1, Bola2, and Kdm6bos, which may mediate the upregulation of ferritin expression by CHIR99021. These findings reveal novel mechanisms of the maintenance of cell stemness and differentiation and provide a theoretical basis for the development of new strategies in stem cell treatment in disease.

摘要

CHIR99021是一种氨基嘧啶衍生物,它能够有效抑制糖原合成激酶3α(GSK-3α)和糖原合成激酶3β(GSK-3β)的活性。作为干细胞培养基的重要组成部分,它在维持细胞干性方面发挥着重要作用。然而,其作用机制尚未完全明确。在本研究中,我们首先发现从小鼠胚胎干细胞(mESCs)培养基中去除CHIR99021会降低铁储存。用CHIR99021处理的Neuro-2a细胞导致铁蛋白表达上调和细胞内铁水平升高,同时伴有GSK3β抑制和Wnt/GSK-3β/β-连环蛋白信号通路激活。此外,铁处理通过影响Neuro-2a细胞中β-连环蛋白的表达激活经典Wnt信号通路。我们的数据通过Wnt/GSK-3β/β-连环蛋白信号通路将铁在维持细胞干性中的作用联系起来,并鉴定出包括Steap1、Bola2和Kdm6bos在内的中间分子,它们可能介导CHIR99021对铁蛋白表达的上调作用。这些发现揭示了维持细胞干性和分化的新机制,并为开发疾病干细胞治疗新策略提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ac/9952287/51163bf498b0/antioxidants-12-00377-g001.jpg

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