化学
G蛋白偶联受体
组胺
人口
细胞生物学
受体
生物物理学
组胺受体
组胺H1受体
活体细胞成像
细胞
生物化学
药理学
生物
敌手
社会学
人口学
作者
Jin Lü,Yunze Yang,Wei Wang,Jinghong Li,Nongjian Tao,Shaopeng Wang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2016-11-01
卷期号:88 (23): 11498-11503
被引量:19
标识
DOI:10.1021/acs.analchem.6b02677
摘要
G protein-coupled receptors (GPCRs) are the largest protein family for cell signal transduction, and most of them are crucial drug targets. Conventional label-free assays lack the spatial information to address the heterogeneous response from single cells after GPCRs activation. Here, we reported a GPCRs study in live cells using plasmonic-based electrochemical impedance microscopy. This label-free optical imaging platform is able to resolve responses from individual cells with subcellular resolution. Using this platform, we studied the histamine mediated GPCRs activation and revealed spatiotemporal heterogeneity of cellular downstream responses. Triphasic responses were observed from individual HeLa cells upon histamine stimulation. A quick peak P1 in less than 10 s was attributed to the GPCRs triggered calcium release. An inverted P2 phase within 1 min was attributed to the alternations of cell-matrix adhesion after the activation of Protein Kinase C (PKC). The main peak (P3) around 3-6 min after the histamine treatment was due to dynamic mass redistribution and showed a dose-dependent response with a half-maximal effective concentration (EC50) of 3.9 ± 1.2 μM. Heterogeneous P3 responses among individual cells were observed, particularly at high histamine concentration, indicating diverse histamine H1 receptor expression level in the cell population.
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