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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Oxidative stress effect on progesterone-induced blocking factor (PIBF) binding to PIBF-receptor in lymphocytes
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Oxidative stress effect on progesterone-induced blocking factor (PIBF) binding to PIBF-receptor in lymphocytes

机译:氧化应激对淋巴细胞中Pibf受体结合的孕酮诱导的阻断因子(PIBF)

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摘要

Receptor-ligand binding is an essential interaction for biological function. Oxidative stress can modify receptors and/or membrane lipid dynamics, thus altering cell physiological functions. The aim of this study is to analyze how oxidative stress may alter receptor-ligand binding and lipid domain distribution in the case of progesterone-induced blocking factor/progesterone-induced blocking factor-receptor. For membrane fluidity regionalization analysis of MEC-1 lymphocytes, two-photon microscopy was used in individual living cells. Lymphocytes were also double stained with AlexaFluor647/progesterone-induced blocking factor and Laurdan to evaluate -induced blocking factor/progesterone-induced blocking factor-receptor distribution in the different membrane domains, under oxidative stress. A new procedure has been developed which quantitatively analyzes the regionalization of a membrane receptor among the lipid domains of different fluidity in the plasma membrane. We have been able to establish a new tool which detects and evaluates lipid raft clustering from two-photon microscopy images of individual living cells. We show that binding of progesterone-induced blocking factor to progesterone-induced blocking factor-receptor causes a rigidification of plasma membrane which is related to an increase of lipid raft clustering. However, this clustering is inhibited under oxidative stress conditions. In conclusion, oxidative stress decreases membrane fluidity, impairs receptor-ligand binding and reduces lipid raft clustering. (C) 2013 Elsevier B.V. All rights reserved.
机译:受体 - 配体结合是生物学功能的基本相互作用。氧化应激可以修饰受体和/或膜脂动力学,从而改变细胞生理功能。本研究的目的是分析氧化应激在孕酮诱导的阻断因子/孕酮诱导的阻断因子受体的情况下可以改变受体 - 配体结合和脂质结构域分布。对于MEC-1淋巴细胞的膜流动性区域化分析,在个体活细胞中使用双光子显微镜。淋巴细胞也与Alexafluor647 /孕酮诱导的阻断因子和Laurdan一起染色,以评估氧化应激在不同膜结构域中的诱导的阻断因子/孕酮诱导的阻断因子受体分布。已经开发了一种新的方法,其定量分析了质膜不同流动性的脂质结构域之间的膜受体的区域化。我们已经能够建立一种新的工具,该工具检测和评估来自个体活细胞的双光子显微镜图像的脂质筏聚类。我们表明孕酮诱导的阻断因子与孕酮诱导的阻断因子受体的结合导致质膜依赖于脂质筏聚类的增加有关。然而,在氧化应激条件下抑制该聚类。总之,氧化应激降低膜流动性,损害受体 - 配体结合并减少脂质筏聚合物。 (c)2013年elestvier b.v.保留所有权利。

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