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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >TRH-receptor mobility and function in intact and cholesterol-depleted plasma membrane of HEK293 cells stably expressing TRH-R-eGFP
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TRH-receptor mobility and function in intact and cholesterol-depleted plasma membrane of HEK293 cells stably expressing TRH-R-eGFP

机译:稳定表达TRH-R-eGFP的HEK293细胞在完整和胆固醇耗尽的质膜中TRH受体的迁移率和功能

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摘要

Here we investigated the effect of disruption of plasma membrane integrity by cholesterol depletion on thyrotropin-releasing hormone receptor (TRH-R) surface mobility in HEK293 cells stably expressing TRH-R-eGFP fusion protein (VTGP cells). Detailed analysis by fluorescence recovery after photobleaching (FRAP) in bleached spots of different sizes indicated that cholesterol depletion did not result in statistically significant alteration of mobile fraction of receptor molecules (M-f). The apparent diffusion coefficient (D-app) was decreased, but this decrease was detectable only under the special conditions of screening and calculation of FRAP data. Analysis of mobility of receptor molecules by raster image correlation spectroscopy (RICS) did not indicate any significant difference between control and cholesterol-depleted cells. Results of our FRAP and RICS experiments may be collectively interpreted in terms of a "membrane fence" model which regards the plasma membrane of living cells as compartmentalized plane where lateral diffusion of membrane proteins is limited to restricted areas by cytoskeleton constraints. Hydrophobic interior of plasma membrane, studied by steady-state and time-resolved fluorescence anisotropy of hydrophobic membrane probe DPH, became substantially more "fluid" and chaotically organized in cholesterol-depleted cells. Decrease of cholesterol level impaired the functional coupling between the receptor and the cognate G proteins of G(q)/G(11) family.
机译:在这里,我们研究了胆固醇消耗破坏质膜完整性对稳定表达TRH-R-eGFP融合蛋白(VTGP细胞)的HEK293细胞中促甲状腺激素释放激素受体(TRH-R)表面迁移率的影响。通过在不同大小的漂白点进行光漂白后的荧光恢复(FRAP)进行的详细分析表明,胆固醇的消耗并未导致受体分子(M-f)的活动级数发生统计学上的显着变化。表观扩散系数(D-app)降低了,但是这种降低只有在筛选和计算FRAP数据的特殊条件下才可以检测到。通过光栅图像相关光谱法(RICS)分析受体分子的迁移率并未显示对照细胞和胆固醇缺乏细胞之间有任何显着差异。我们的FRAP和RICS实验的结果可以用“膜栅栏”模型来统一解释,该模型将活细胞的质膜视为分隔的平面,其中膜蛋白的横向扩散受细胞骨架限制而限制在受限区域内。通过疏水膜探针DPH的稳态和时间分辨荧光各向异性研究了质膜的疏水内部,在缺乏胆固醇的细胞中变得更加“流体化”,并且组织混乱。胆固醇水平的降低损害了受体与G(q)/ G(11)家族的同源G蛋白之间的功能耦合。

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