Real-time evaluation of human secretin receptor activity using cytosensor microphysiometry

• Published in: Journal of cellular biochemistry Vol. 72; no. 4; pp. 517 - 527
• Main Authors: Ng, Samuel S.M., Pang, Ronald T.K., Chow, Billy K.C., Cheng, Christopher H.K.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 15.03.1999
• Subjects: 1-Methyl-3-isobutylxanthine - pharmacology; Animals; Biotinylation; cAMP; CHO Cells; Colforsin - pharmacology; Cricetinae; Cyclic AMP - metabolism; Cyclic AMP-Dependent Protein Kinases - metabolism; Cytosensor microphysiometry; human secretin receptor; Humans; Isoquinolines - pharmacology; Microscopy, Fluorescence; Receptors, G-Protein-Coupled; Receptors, Gastrointestinal Hormone - metabolism; Secretin - pharmacology; Signal Transduction; Sulfonamides; Transfection
• ISSN: 0730-2312; 1097-4644
• DOI: 10.1002/(SICI)1097-4644(19990315)72:4<517::AID-JCB7>3.0.CO;2-1

Human secretin receptor is a G protein‐coupled receptor that is functionally linked to the cAMP second messenger system by stimulation of adenylate cyclase. To functionally characterize the receptor and evaluate its signal transduction pathway, the full‐length human secretin receptor cDNA was subcloned into the mammalian expression vector pRc/CMV and expressed in cultured CHO cells. Intracellular cAMP accumulation of the stably transfected cells was measured by a radioimmunoassay (RIA), while the extracellular acidification rate was measured by the Cytosensor microphysiometer. Human secretin and biotinylated human secretin were equipotent in both assays in a dose‐dependent manner. The EC50 values of stimulating the intracellular cAMP accumulation and the extracellular acidification rate were 0.2–0.5 nM and 0.1 nM, respectively, indicating that microphysiometry is more sensitive than the cAMP assay in monitoring ligand stimulation of the human secretin receptor. The secretin‐stimulated response could be mimicked by forskolin and augmented by the phosphodiesterase inhibitor 3‐isobutyl‐1‐methylxanthine, indicating that the extracellular acidification response is positively correlated with intracellular cAMP level. The response could be abolished by the protein kinase A inhibitor H‐89, suggesting that protein kinase A plays an essential role in the intracellular signaling of the receptor. Upon repeated stimulation by the ligand, the peak acidification responses did not change significantly at both physiological (0.03 nM and 3 nM) and pharmacological (0.3 μM) concentrations of human secretin, suggesting that the human secretin receptor did not exhibit robust homologous desensitization. J. Cell. Biochem. 72:517–527, 1999. © 1999 Wiley‐Liss, Inc.