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超分辨率成像揭示的表皮生长因子受体(EGFR)膜聚集的机制洞察

Mechanistic insights into EGFR membrane clustering revealed by super-resolution imaging.

作者信息

Gao Jing, Wang Ye, Cai Mingjun, Pan Yangang, Xu Haijiao, Jiang Junguang, Ji Hongbin, Wang Hongda

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, P.R. China.

出版信息

Nanoscale. 2015 Feb 14;7(6):2511-9. doi: 10.1039/c4nr04962d.

DOI:10.1039/c4nr04962d
PMID:25569174
Abstract

The clustering of membrane receptors such as EGFR is critical for various biological processes, for example cell signaling and tumorigenesis. However, the mechanism involved remains poorly understood. Here, we used a super resolution imaging technique, which has shattered the longstanding resolution barrier of light diffraction, to investigate the distribution of membrane EGFR on apical or basal surfaces of COS-7 cells and on the surface of suspended COS-7 cells. Our data show that more and larger EGFR clusters are detected on the apical surface in comparison with those on the basal surface and this difference is not affected by the EGFR activation state, whereas suspended COS-7 cells exhibit a moderate clustering state and a homogeneous distribution pattern, indicating that the external environment surrounding the cell membrane is the decisive factor in the EGFR clustering pattern. A dual-color dSTORM image reveals the significant colocalization of EGFR and lipid rafts; interestingly MβCD treatment leads to a dramatic decrease of the amount and size of EGFR clusters on both apical and basal surfaces, highlighting a key role of lipid rafts in EGFR cluster formation. Altogether, our results illustrate the distribution pattern of EGFR in polarized cells and uncover the essential role of lipid rafts in EGFR cluster maintenance.

摘要

诸如表皮生长因子受体(EGFR)等膜受体的聚集对于多种生物学过程至关重要,例如细胞信号传导和肿瘤发生。然而,其中涉及的机制仍知之甚少。在此,我们使用了一种超分辨率成像技术,该技术打破了长期以来光衍射的分辨率障碍,以研究膜EGFR在COS-7细胞顶端或基底表面以及悬浮COS-7细胞表面的分布。我们的数据表明,与基底表面相比,在顶端表面检测到更多且更大的EGFR簇,并且这种差异不受EGFR激活状态的影响,而悬浮的COS-7细胞呈现出中等聚集状态和均匀分布模式,这表明细胞膜周围的外部环境是EGFR聚集模式的决定性因素。双色直接随机光学重建显微镜(dSTORM)图像揭示了EGFR与脂筏的显著共定位;有趣的是,甲基-β-环糊精(MβCD)处理导致顶端和基底表面上EGFR簇的数量和大小显著减少,突出了脂筏在EGFR簇形成中的关键作用。总之,我们的结果阐明了EGFR在极化细胞中的分布模式,并揭示了脂筏在EGFR簇维持中的重要作用。

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