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四氢叶酸通过 PTEN/Akt/mTOR 通路缓解氧化应激对神经干细胞增殖的抑制作用。

Tetrahydrofolate Alleviates the Inhibitory Effect of Oxidative Stress on Neural Stem Cell Proliferation through PTEN/Akt/mTOR Pathway.

机构信息

Department of Neurosurgery and Key Laboratory of Neurotrauma, Southwest Hospital, Third Military Medical University (Army Medical University), 400038 Chongqing, China.

Department of Neurosurgery, The 908th Hospital of Chinese People's Liberation Army Joint Logistic Support Force, 330002 Nanchang, Jiangxi, China.

出版信息

Oxid Med Cell Longev. 2022 Feb 27;2022:9021474. doi: 10.1155/2022/9021474. eCollection 2022.

Abstract

Neural stem cell (NSC) proliferation is the initial step for NSC participating in neurorehabilitation after central nervous system (CNS) injury. During this process, oxidative stress is always involved in restricting the regenerative ability of NSC. Tetrahydrofolate (THF) is susceptible to oxidative stress and exhibits a high antioxidant activity. While its effect on NSC proliferation under oxidative stress condition remains obscure. Here, NSC were isolated from embryonic mice and identified using immunofluorescent staining. Meanwhile, the results showed that THF (5 M and 10 M) attenuated oxidative stress induced by 50 M hydrogen peroxide (HO) in NSC using mitochondrial hydroxyl radical detection and Western blotting assays. Afterward, administration of THF markedly alleviated the inhibitory effect of oxidative stress on NSC proliferation, which was evidenced by Cell Counting Kit-8 (CCK8), neurosphere formation, and immunofluorescence of Ki67 assays. Thereafter, the results revealed that PTEN/Akt/mTOR signaling pathway played a pivotal role in counteracting oxidative stress to rescue the inhibitory effect of oxidative stress on NSC proliferation using Western blotting assays and gene knockdown techniques. Collectively, these results demonstrate that THF mitigates the inhibitory effect of oxidative stress on NSC proliferation via PTEN/Akt/mTOR signaling pathway, which provides evidence for administrating THF to potentiate the neuro-reparative capacity of NSC in the treatment of CNS diseases with the presence of oxidative stress.

摘要

神经干细胞(NSC)增殖是 NSC 参与中枢神经系统(CNS)损伤后神经康复的初始步骤。在这个过程中,氧化应激总是参与限制 NSC 的再生能力。四氢叶酸(THF)易受氧化应激影响,表现出较高的抗氧化活性。然而,其在氧化应激条件下对 NSC 增殖的影响尚不清楚。在这里,我们从胚胎小鼠中分离出 NSC,并通过免疫荧光染色进行鉴定。同时,结果表明,THF(5μM 和 10μM)通过线粒体羟基自由基检测和 Western blot 分析减轻了 50μM 过氧化氢(HO)诱导的 NSC 氧化应激。随后,THF 的给药显著减轻了氧化应激对 NSC 增殖的抑制作用,这可以通过细胞计数试剂盒-8(CCK8)、神经球形成和 Ki67 免疫荧光检测来证明。此后,结果表明,PTEN/Akt/mTOR 信号通路在通过 Western blot 分析和基因敲低技术拮抗氧化应激以挽救氧化应激对 NSC 增殖的抑制作用方面发挥了关键作用。总之,这些结果表明,THF 通过 PTEN/Akt/mTOR 信号通路减轻氧化应激对 NSC 增殖的抑制作用,为在存在氧化应激的情况下,用 THF 增强 NSC 的神经修复能力来治疗 CNS 疾病提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c169/8898800/1d0a8e0364d2/OMCL2022-9021474.001.jpg

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