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Inhibition of autophagy prevents irradiation-induced neural stem and progenitor cell death in the juvenile mouse brain

机译:抑制自噬可防止辐射诱导的幼鼠大脑神经干和祖细胞死亡

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摘要

Radiotherapy is an effective tool in the treatment of malignant brain tumors. However, damage to brain stem and progenitor cells constitutes a major problem and is associated with long-term side effects. Autophagy has been shown to be involved in cell death, and the purpose of this study was to evaluate the effect of autophagy inhibition on neural stem and progenitor cell death in the juvenile brain. Ten-day-old selective Atg7 knockout (KO) mice and wild-type (WT) littermates were subjected to a single 6Gy dose of whole-brain irradiation. Cell death and proliferation as well as microglia activation and inflammation were evaluated in the dentate gyrus of the hippocampus and in the cerebellum at 6?h after irradiation. We found that cell death was reduced in Atg7 KO compared with WT mice at 6?h after irradiation. The number of activated microglia increased significantly in both the dentate gyrus and the cerebellum of WT mice after irradiation, but the increase was lower in the Atg7 KO mice. The levels of proinflammatory cytokines and chemokines decreased, especially in the cerebellum, in the Atg7 KO group. These results suggest that autophagy might be a potential target for preventing radiotherapy-induced neural stem and progenitor cell death and its associated long-term side effects.
机译:放射疗法是治疗恶性脑肿瘤的有效工具。然而,对脑干和祖细胞的损害是一个主要问题,并且与长期副作用有关。自噬已被证明与细胞死亡有关,这项研究的目的是评估自噬抑制对少年脑神经干细胞和祖细胞死亡的影响。对十天大的选择性Atg7基因敲除(KO)小鼠和野生型(WT)同窝仔进行6Gy剂量的全脑照射。在照射后6小时,评估海马齿状回和小脑的细胞死亡和增殖以及小胶质细胞活化和炎症。我们发现,与WT小鼠相比,Atg7 KO的细胞死亡在辐射后的6?h减少了。辐射后WT小鼠的齿状回和小脑中活化的小胶质细胞的数量均显着增加,但Atg7 KO小鼠的活化小胶质细胞的数量则较少。 Atg7 KO组的促炎细胞因子和趋化因子水平下降,尤其是小脑。这些结果表明自噬可能是预防放射治疗引起的神经干细胞和祖细胞死亡及其相关的长期副作用的潜在目标。

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