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神经节苷脂诱导的自噬性细胞死亡和星形胶质细胞激活中 NF-κB 作为共同信号通路。

NF-κB as a common signaling pathway in ganglioside-induced autophagic cell death and activation of astrocytes.

机构信息

Department of Pharmacology, Brain Science and Engineering Institute, CMRI, Kyungpook National University School of Medicine, Daegu, Republic of Korea.

出版信息

J Neuroimmunol. 2010 Sep 14;226(1-2):66-72. doi: 10.1016/j.jneuroim.2010.05.037. Epub 2010 Jun 15.

Abstract

We have previously shown that gangliosides induce autophagic cell death of brain astrocytes. As gangliosides are also known to induce inflammatory activation of astrocytes, we hypothesized that a canonical inflammatory signaling pathway NF-κB might be involved in the ganglioside-induced astrocyte cell death and activation. Using cultured mouse astrocytes and C6 rat glioma cell line, we determined the role of NF-κB in autophagic cell death and nitric oxide (NO) production in astrocytes. Gangliosides induced iNOS/GFAP expression and NF-κB activation. IKK inhibitor SC-514 and NF-κB inhibitor PDTC reduced ganglioside-induced astrocyte activation and cell death. Moreover, inhibition of NF-κB pathway also attenuated autophagy of astrocytes. Rho subfamily of small G proteins antagonized the ganglioside-induced astrocyte cell death as well as activation pathways. Taken together, IKK/NF-κB may constitute one of the common signaling pathways in ganglioside-induced astrocyte activation and autophagic cell death, and may play an important role in the ganglioside intracellular signaling that regulates astrocyte physiology and pathology.

摘要

我们之前已经表明,神经节苷脂会诱导大脑星形胶质细胞发生自噬性细胞死亡。由于神经节苷脂也被认为会引发星形胶质细胞的炎症激活,我们假设经典的炎症信号通路 NF-κB 可能参与了神经节苷脂诱导的星形胶质细胞死亡和激活。我们使用培养的小鼠星形胶质细胞和 C6 大鼠神经胶质瘤细胞系,确定了 NF-κB 在星形胶质细胞自噬性细胞死亡和一氧化氮 (NO) 产生中的作用。神经节苷脂诱导 iNOS/GFAP 表达和 NF-κB 激活。IKK 抑制剂 SC-514 和 NF-κB 抑制剂 PDTC 减少了神经节苷脂诱导的星形胶质细胞激活和死亡。此外,抑制 NF-κB 通路也减弱了星形胶质细胞的自噬作用。Rho 亚家族的小 G 蛋白拮抗了神经节苷脂诱导的星形胶质细胞死亡以及激活途径。综上所述,IKK/NF-κB 可能构成神经节苷脂诱导的星形胶质细胞激活和自噬性细胞死亡的共同信号通路之一,并可能在调节星形胶质细胞生理和病理的神经节苷脂细胞内信号转导中发挥重要作用。

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