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肿瘤坏死因子-α与白细胞介素-4或白细胞介素-13协同诱导人角膜细胞中嗜酸性粒细胞趋化因子的表达。

Synergistic induction of eotaxin expression in human keratocytes by TNF-alpha and IL-4 or IL-13.

作者信息

Kumagai N, Fukuda K, Ishimura Y, Nishida T

机构信息

Department of Ophthalmology, Yamaguchi University School of Medicine, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2000 May;41(6):1448-53.

Abstract

PURPOSE

To investigate the effects of tumor necrosis factor (TNF)-alpha, interleukin (IL)4, and IL-13 on expression of the chemokine eotaxin by cultured human keratocytes.

METHODS

Cultured human keratocytes were incubated with various combinations and concentrations of TNF-alpha, IL-4, and IL-13. The concentration of eotaxin in the culture supernatant was subsequently measured by enzyme-linked immunosorbent assay, and the amount of eotaxin mRNA in cell lysates was determined by reverse transcription-polymerase chain reaction analysis.

RESULTS

Keratocytes incubated in the absence of cytokines did not release detectable amounts of eotaxin into the culture medium. Whereas incubation of keratocytes with TNF-alpha, IL-4, or IL-13 alone or with the combination of IL-4 and IL-13 had only a small effect on eotaxin release, exposure of the cells to TNF-alpha in combination with either IL-4 or IL-13 resulted in a marked increase in eotaxin production that was both time and dose dependent. The abundance of eotaxin mRNA in keratocytes was also increased in a synergistic manner by incubation of cells with TNF-alpha together with either IL-4 or IL-13.

CONCLUSIONS

Stimulation of human keratocytes with the combination of TNF-alpha and either IL-4 or IL-13 resulted in synergistic increases in both the abundance of eotaxin mRNA and the release of eotaxin protein. This cytokine-induced increase in eotaxin production by keratocytes may contribute to eosinophil infiltration in inflammatory ocular diseases such as vernal keratoconjunctivitis.

摘要

目的

研究肿瘤坏死因子(TNF)-α、白细胞介素(IL)-4和IL-13对培养的人角膜细胞趋化因子嗜酸性粒细胞趋化蛋白表达的影响。

方法

将培养的人角膜细胞与TNF-α、IL-4和IL-13的不同组合及浓度进行孵育。随后通过酶联免疫吸附测定法测量培养上清液中嗜酸性粒细胞趋化蛋白的浓度,并通过逆转录-聚合酶链反应分析确定细胞裂解物中嗜酸性粒细胞趋化蛋白mRNA的量。

结果

在无细胞因子的情况下孵育的角膜细胞不会向培养基中释放可检测量的嗜酸性粒细胞趋化蛋白。虽然单独用TNF-α、IL-4或IL-13孵育角膜细胞,或用IL-4和IL-13的组合孵育,对嗜酸性粒细胞趋化蛋白的释放只有很小的影响,但将细胞暴露于TNF-α与IL-4或IL-13的组合中会导致嗜酸性粒细胞趋化蛋白产量显著增加,且具有时间和剂量依赖性。通过将细胞与TNF-α以及IL-4或IL-13一起孵育,角膜细胞中嗜酸性粒细胞趋化蛋白mRNA的丰度也以协同方式增加。

结论

用TNF-α与IL-4或IL-13的组合刺激人角膜细胞会导致嗜酸性粒细胞趋化蛋白mRNA丰度和嗜酸性粒细胞趋化蛋白的释放协同增加。这种由细胞因子诱导的角膜细胞嗜酸性粒细胞趋化蛋白产量增加可能导致嗜酸性粒细胞浸润到如春季角结膜炎等炎症性眼病中。

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