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人乳腺癌细胞系MCF-7中诱导型和内皮型一氧化氮合酶的研究——雌激素对内皮型一氧化氮合酶有影响,但对诱导型一氧化氮合酶没有影响。

Investigations on the inducible and endothelial nitric oxide synthases in human breast cancer cell line MCF-7 - estrogen has an influence on e-NOS, but not on i-NOS.

作者信息

Loibl Sibylle, Bratengeier Jutta, Farines Vincent, von Minckwitz Gunter, Spänkuch Birgit, Schini-Kerth Valérie, Nepveu Françoise, Strebhardt Klaus, Kaufmann Manfred

机构信息

Department of Gynecology and Obstetrics, University of Frankfurt, Theodor-Stern-Kai 7-9, 60590 Frankfurt am Main, Germany.

出版信息

Pathol Res Pract. 2006;202(1):1-7. doi: 10.1016/j.prp.2005.10.003. Epub 2005 Dec 2.

Abstract

As a model for hormone-dependent breast cancer, we studied the MCF-7 cell line to examine differences in the stimulation of the inducible (i) and endothelial (e) nitric oxide synthase (NOS) and the role of 17beta-estradiol (E(2)). MCF-7 cells were stimulated with (a) E(2) (10(-8)M) and (b) a combination of different cytokines such as interleukin-1 beta (Il-1beta), tumor necrosis factor alpha (TNF-alpha) and interferon gamma (INF-gamma), and lipopolysaccharide (LPS). e-NOS and i-NOS proteins were measured using Western blot analysis. Using the Griess method nitric oxide (NO) was estimated by assessing the stable product nitrite (NO(2-)) in the culture medium, and a direct method, employing EPR spin trapping also was used. Western blot analysis revealed the presence of e-NOS and i-NOS in MCF-7 cells. In Western blot analysis, e-NOS, but not i-NOS, expression could be stimulated by E(2). An increase in NO(2-) was noted after stimulation of MCF-7 using different combinations of cytokines Il-1beta, TNFalpha and INFgamma, and LPS, but not after E(2). In conclusion, e-NOS and i-NOS are weakly expressed in the MCF-7 cell line, but are stimulated differently. The MCF-7 cell may contain both a constitutive NOS and an inducible NOS.

摘要

作为激素依赖性乳腺癌的模型,我们研究了MCF-7细胞系,以检测诱导型(i)和内皮型(e)一氧化氮合酶(NOS)的刺激差异以及17β-雌二醇(E₂)的作用。用(a)E₂(10⁻⁸M)和(b)不同细胞因子如白细胞介素-1β(Il-1β)、肿瘤坏死因子-α(TNF-α)、干扰素-γ(INF-γ)和脂多糖(LPS)的组合刺激MCF-7细胞。使用蛋白质印迹分析测定e-NOS和i-NOS蛋白。采用Griess法,通过评估培养基中稳定产物亚硝酸盐(NO₂⁻)来估计一氧化氮(NO),还使用了采用电子顺磁共振自旋捕获的直接方法。蛋白质印迹分析显示MCF-7细胞中存在e-NOS和i-NOS。在蛋白质印迹分析中,E₂可刺激e-NOS而非i-NOS的表达。使用细胞因子Il-1β、TNF-α和INF-γ以及LPS的不同组合刺激MCF-7后,NO₂⁻增加,但E₂刺激后未增加。总之,e-NOS和i-NOS在MCF-7细胞系中表达较弱,但刺激方式不同。MCF-7细胞可能同时含有组成型NOS和诱导型NOS。

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