TY - JOUR
T1 - Label-free imaging of histamine mediated G protein-coupled receptors activation in live cells
AU - Lu, Jin
AU - Yang, Yunze
AU - Wang, Wei
AU - Li, Jinghong
AU - Tao, Nongjian
AU - Wang, Shaopeng
N1 - Funding Information:
We acknowledge financial support from National Institute of Health (8R21GM103396, 5R01GM107165), National Science Foundation (#1151105), and National Natural Science Foundation of China (No. 21621003, No. 21235004, No. 21327806).
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/12/6
Y1 - 2016/12/6
N2 - 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 dosedependent 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.
AB - 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 dosedependent 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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U2 - 10.1021/acs.analchem.6b02677
DO - 10.1021/acs.analchem.6b02677
M3 - Article
C2 - 27802015
AN - SCOPUS:85035238491
SN - 0003-2700
VL - 88
SP - 11498
EP - 11503
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 23
ER -