SIRT1-driven mechanism: sevoflurane's interference with mESC neural differentiation via PRRX1/DRD2 cascade.

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Feifei Liu, Chenguang Li
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引用次数: 0

Abstract

Investigating the sevoflurane-induced perturbation in the differentiation of mouse embryonic stem cells (mESCs) into neural stem cells (mNSCs), our study delineates a novel SIRT1/PRRX1/DRD2/PKM2/NRF2 axis as a key player in this intricate process. Sevoflurane treatment hindered mESC differentiation, evidenced by altered expression patterns of pluripotency and neural lineage markers. Mechanistically, sevoflurane downregulated Sirt1, setting in motion a signaling cascade. Sevoflurane may inhibit PKM2 dimerization and NRF2 signaling pathway activation by inhibiting the expression of SIRT1 and its downstream genes Prrx1 and DRD2, ultimately inhibiting mESCs differentiation into mNSCs. These findings contribute to our understanding of the molecular basis of sevoflurane-induced neural toxicity, presenting a potential avenue for therapeutic intervention in sevoflurane-induced perturbation in the differentiation of mESCs into mNSCs by modulating the SIRT1/PRRX1/DRD2/PKM2/NRF2 axis.

SIRT1驱动机制:七氟烷通过PRRX1/DRD2级联干扰mESC神经分化
我们的研究调查了七氟烷诱导的小鼠胚胎干细胞(mESCs)向神经干细胞(mNSCs)分化过程中的扰动,发现新的SIRT1/PRRX1/DRD2/PKM2/NRF2轴是这一复杂过程中的关键参与者。七氟烷处理阻碍了mESC的分化,多能性和神经系标志物表达模式的改变证明了这一点。从机理上讲,七氟烷下调了Sirt1,启动了信号级联。七氟烷可能通过抑制 SIRT1 及其下游基因 Prrx1 和 DRD2 的表达来抑制 PKM2 的二聚化和 NRF2 信号通路的激活,最终抑制 mESCs 分化为 mNSCs。这些发现有助于我们理解七氟烷诱导的神经毒性的分子基础,为通过调节SIRT1/PRRX1/DRD2/PKM2/NRF2轴来干预七氟烷诱导的mESCs向mNSCs分化过程提供了潜在的治疗途径。
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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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