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肿瘤坏死因子α增强γ干扰素诱导的少突胶质前体细胞死亡。

TNFalpha potentiates IFNgamma-induced cell death in oligodendrocyte progenitors.

作者信息

Andrews T, Zhang P, Bhat N R

机构信息

Department of Neurology, Medical University of South Carolina, Charleston 29425, USA.

出版信息

J Neurosci Res. 1998 Dec 1;54(5):574-83. doi: 10.1002/(SICI)1097-4547(19981201)54:5<574::AID-JNR2>3.0.CO;2-0.

Abstract

Oligodendrocytes in multiple sclerosis brain may be under a direct attack by proinflammatory cytokines, particularly tumor necrosis factor-alpha (TNFalpha) and interferon-gamma (IFNgamma). In this study, we have examined the in vitro cytotoxic effects of the two cytokines, individually and in combination, on oligodendrocyte lineage cells using morphological criteria, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide reduction assay (MTT), terminal deoxynucleotide transferase-mediated dUTP nick end-labeling (TUNEL), and agarose-gel electrophoretic analysis of fragmented DNA. IFNgamma exerted a dose-dependent cytotoxic effect on cultured CG4 cells, an oligodendrocyte progenitor cell line, and in primary cultures of purified oligodendrocyte progenitors. TNFalpha, while by itself being only mildly toxic, greatly potentiated the cytotoxicity of IFNgamma. The cytokine effects were developmentally modified in that their cytotoxic and cooperative effects became less evident in more differentiated cells. A cell-permeable peptide inhibitor (i.e., z-VAD.fmk) of caspases partially suppressed apoptotic changes elicited by the cytokine combination in CG4 cells but not in primary oligodendrocytes. Reverse transcriptase polymerase chain reaction (RT-PCR) analysis of mRNA prepared from cytokine-treated cultures revealed an increased expression of the death receptor, Fas. The results suggest particular vulnerability of oligodendrocyte progenitors to a combination of TNFalpha and IFNgamma involving an activation of the cell death program.

摘要

多发性硬化症患者大脑中的少突胶质细胞可能受到促炎细胞因子的直接攻击,尤其是肿瘤坏死因子-α(TNFα)和干扰素-γ(IFNγ)。在本研究中,我们使用形态学标准、3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐还原试验(MTT)、末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)以及片段化DNA的琼脂糖凝胶电泳分析,研究了这两种细胞因子单独及联合作用对少突胶质细胞系细胞的体外细胞毒性作用。IFNγ对培养的CG4细胞(一种少突胶质细胞祖细胞系)以及纯化的少突胶质细胞祖细胞原代培养物具有剂量依赖性细胞毒性作用。TNFα本身毒性较小,但能显著增强IFNγ的细胞毒性。细胞因子的作用在发育过程中有所改变,即它们的细胞毒性和协同作用在分化程度较高的细胞中不太明显。一种细胞可渗透的半胱天冬酶肽抑制剂(即z-VAD.fmk)部分抑制了细胞因子组合在CG4细胞中引发的凋亡变化,但对原代少突胶质细胞无效。对细胞因子处理的培养物制备的mRNA进行逆转录聚合酶链反应(RT-PCR)分析显示,死亡受体Fas的表达增加。结果表明,少突胶质细胞祖细胞对TNFα和IFNγ的组合特别敏感,涉及细胞死亡程序的激活。

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