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双雄对决:神经干细胞遭遇缺氧。

A Tale of Two: When Neural Stem Cells Encounter Hypoxia.

机构信息

Department of Anesthesiology, The First Hospital of China Medical University, Shenyang, China.

出版信息

Cell Mol Neurobiol. 2023 Jul;43(5):1799-1816. doi: 10.1007/s10571-022-01293-6. Epub 2022 Oct 29.

Abstract

Normoxia is defined as an oxygen concentration of 20.9%, as in room air, whereas hypoxia refers to any oxygen concentration less than this. Any physiological oxygen deficiency or tissue oxygen deficiency relative to demand is called hypoxia. Neural stem cells (NSCs) are multipotent stem cells that can differentiate into multiple cell lines such as neurons, oligodendrocytes, and astrocytes. Under hypoxic conditions, the apoptosis rate of NSCs increases remarkably in vitro or in vivo. However, some hypoxia promotes the proliferation and differentiation of NSCs. The difference is related to the oxygen concentration, the duration of hypoxia, the hypoxia tolerance threshold of the NSCs, and the tissue source of the NSCs. The main mechanism of hypoxia-induced proliferation and differentiation involves an increase in cyclin and erythropoietin concentrations, and hypoxia-inducible factors play a key role. Multiple molecular pathways are activated during hypoxia, including Notch, Wnt/β-catenin, PI3K/Akt, and altered microRNA expression. In addition, we review the protective effect of exogenous NSCs transplantation on ischemic or anoxic organs, the therapeutic potential of hypoxic preconditioning on exogenous NSCs and clinical application of NSCs.

摘要

常氧定义为氧气浓度为 20.9%,如在室内空气中,而缺氧是指任何低于此浓度的氧气。任何与需求相比的生理氧气不足或组织氧气不足都称为缺氧。神经干细胞(NSCs)是多能干细胞,可以分化为多种细胞系,如神经元、少突胶质细胞和星形胶质细胞。在缺氧条件下,NSCs 的体外或体内凋亡率显著增加。然而,一些缺氧促进 NSCs 的增殖和分化。这种差异与氧浓度、缺氧持续时间、NSCs 的缺氧耐受阈值以及 NSCs 的组织来源有关。缺氧诱导增殖和分化的主要机制涉及细胞周期蛋白和促红细胞生成素浓度的增加,缺氧诱导因子起着关键作用。在缺氧期间,多个分子途径被激活,包括 Notch、Wnt/β-catenin、PI3K/Akt 和改变的 microRNA 表达。此外,我们还综述了外源性 NSCs 移植对缺血或缺氧器官的保护作用、缺氧预处理对外源性 NSCs 的治疗潜力和 NSCs 的临床应用。

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A Tale of Two: When Neural Stem Cells Encounter Hypoxia.双雄对决:神经干细胞遭遇缺氧。
Cell Mol Neurobiol. 2023 Jul;43(5):1799-1816. doi: 10.1007/s10571-022-01293-6. Epub 2022 Oct 29.

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