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CXCL1 通过刺激 APP/PS1 小鼠中活性氧的产生促进神经干细胞的增殖。

CXCL1 promotes the proliferation of neural stem cells by stimulating the generation of reactive oxygen species in APP/PS1 mice.

机构信息

Department of Developmental Cell Biology, Key Laboratory of Cell Biology, Ministry of Public Health, Key Laboratory of Medical Cell Biology, Ministry of Education, China Medical University, No.77 Puhe Road, Shenyang North New Area, Shenyang, Liaoning Province, PR China.

Department of Geriatrics, Shengjing Hospital of China Medical University, No.36 Sanhao Street, Heping District, Shenyang, Liaoning Province, PR China.

出版信息

Biochem Biophys Res Commun. 2019 Jul 12;515(1):201-206. doi: 10.1016/j.bbrc.2019.05.130. Epub 2019 May 27.

Abstract

PURPOSE

Elevated levels of CXCL1 were observed in the cerebrospinal fluid of patients with early Alzheimer's disease, which may affect neural stem cells in the subventricular zone. We used APP/PS1 mice and neural stem cells to elucidate the role of CXCL1 in Alzheimer's disease.

METHODS & RESULTS: We detected CXCL1 in cerebrospinal fluid (CSF), activated macrophages, and microglia suggesting that macrophages may contribute to elevated CXCL1 in the CSF of middle-aged APP/PS1 mice. Proliferation and differentiation of neural stem cells were further analyzed and the results suggested that CXCL1 promotes the proliferation of neural stem cells and inhibits their differentiation into astrocytes. In order to determine how CXCL1 exerts these effects, we analyzed intracellular reactive oxygen species, cell signaling, and performed in vivo recovery experiments. Our results suggest that CXCL1 promotes neural stem cell proliferation through a mechanism involving the production of reactive oxygen species and the PI3K/Akt pathway.

CONCLUSION

In APP/PS1 mice, macrophage-derived CXCL1 can promote the proliferation of neural stem cells in the subventricular zone via the NOX2-ROS-PI3K/Akt pathway.

摘要

目的

在早期阿尔茨海默病患者的脑脊液中观察到 CXCL1 水平升高,这可能影响侧脑室下区的神经干细胞。我们使用 APP/PS1 小鼠和神经干细胞来阐明 CXCL1 在阿尔茨海默病中的作用。

方法和结果

我们在脑脊液 (CSF)、活化的巨噬细胞和小胶质细胞中检测到 CXCL1,这表明巨噬细胞可能有助于中年 APP/PS1 小鼠 CSF 中 CXCL1 的升高。进一步分析了神经干细胞的增殖和分化,结果表明 CXCL1 促进神经干细胞的增殖,并抑制其分化为星形胶质细胞。为了确定 CXCL1 如何发挥这些作用,我们分析了细胞内活性氧、细胞信号转导,并进行了体内恢复实验。我们的结果表明,CXCL1 通过产生活性氧和 PI3K/Akt 途径促进神经干细胞的增殖。

结论

在 APP/PS1 小鼠中,巨噬细胞衍生的 CXCL1 通过 NOX2-ROS-PI3K/Akt 途径促进侧脑室下区神经干细胞的增殖。

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