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干扰素-γ与肿瘤坏死因子-α对人胰岛细胞的细胞毒性作用。

Cytotoxic effect of IFN-gamma plus TNF-alpha on human islet cells.

作者信息

Soldevila G, Buscema M, Doshi M, James R F, Bottazzo G F, Pujol-Borrell R

机构信息

Laboratorio the Inmunología, Hospital Universitario Germans Trias i Pujol, (Barcelona), Spain.

出版信息

J Autoimmun. 1991 Apr;4(2):291-306. doi: 10.1016/0896-8411(91)90025-8.

Abstract

We have previously reported that the combination of IFN-gamma plus TNF-alpha is able to induce the de novo expression of HLA class II on human beta cells. In the present study, we have investigated the effect of these cytokines, alone or in combination, on the function and viability of human islet cells in vitro. Three hour insulin release was markedly reduced in human islet monolayer cultures after 4 days' exposure to 1000 U/ml of the combination TNF-alpha plus IFN-gamma (36.7 +/- 7.7, % of the control +/- SEM) or to TNF-alpha alone (49.5 +/- 7% of the control) while IFN-gamma had little effect. On direct inspection cell damage was clearly detected only in the cultures treated with TNF-alpha plus IFN-gamma in which staining by indirect immunofluorescence (IFL) for insulin revealed that the number of beta cells was also significantly reduced, thus suggesting a real cytotoxic effect of this cytokine combination. This effect was not beta cell specific since glucagon release and the number of alpha cells were also reduced in the cultures exposed to IFN-gamma plus TNF-alpha. 51Cr release experiments supported the cytoxicity of these cytokines to normal islet cells. There was a time course relationship between class II induction (2 days) and the cytotoxic effect of IFN-gamma plus TNF-alpha (4 days) on the same islet cells. In conclusion, these results indicate that the combination of IFN-gamma and TNF-alpha exerts a cytotoxic effect on human islet cells in vitro.

摘要

我们之前曾报道,γ干扰素(IFN-γ)与肿瘤坏死因子-α(TNF-α)联合使用能够诱导人β细胞重新表达II类组织相容性抗原(HLA)。在本研究中,我们调查了这些细胞因子单独或联合使用时对人胰岛细胞体外功能和生存能力的影响。在人胰岛单层培养物中,暴露于1000 U/ml的TNF-α与IFN-γ联合制剂(36.7±7.7,相对于对照组的百分比±标准误)或单独的TNF-α(49.5±7%的对照组)4天后,三小时胰岛素释放量显著降低,而IFN-γ单独作用时影响很小。直接观察发现,仅在经TNF-α与IFN-γ联合处理的培养物中可明显检测到细胞损伤,其中胰岛素间接免疫荧光(IFL)染色显示β细胞数量也显著减少,从而提示这种细胞因子组合具有真正的细胞毒性作用。这种作用并非β细胞特异性的,因为在暴露于IFN-γ加TNF-α的培养物中,胰高血糖素释放和α细胞数量也减少。51铬(51Cr)释放实验支持了这些细胞因子对正常胰岛细胞的细胞毒性。II类抗原诱导(2天)与IFN-γ加TNF-α对同一胰岛细胞的细胞毒性作用(4天)之间存在时间进程关系。总之,这些结果表明,IFN-γ和TNF-α联合使用在体外对人胰岛细胞发挥细胞毒性作用。

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