A subscription to JoVE is required to view this content. Sign in or start your free trial.
The protocol presented in this study illustrates the effectiveness of the cAMP Difference Detector In Situ in measuring cAMP through two methods. One method utilizes a 96-well plate reading spectrophotometer with HEK-293 cells. The other method demonstrates individual HASM cells under a fluorescent microscope.
cAMP Difference Detector In Situ (cADDis) is a novel biosensor that allows for the continuous measurement of cAMP levels in living cells. The biosensor is created from a circularly permuted fluorescent protein linked to the hinge region of Epac2. This creates a single fluorophore biosensor that displays either increased or decreased fluorescence upon binding of cAMP. The biosensor exists in red and green upward versions, as well as green downward versions, and several red and green versions targeted to subcellular locations. To illustrate the effectiveness of the biosensor, the green downward version, which decreases in fluorescence upon cAMP binding, was used. Two protocols using this sensor are demonstrated: one utilizing a 96-well plate reading spectrophotometer compatible with high-throughput screening and another utilizing single-cell imaging on a fluorescent microscope. On the plate reader, HEK-293 cells cultured in 96-well plates were stimulated with 10 µM forskolin or 10 nM isoproterenol, which induced rapid and large decreases in fluorescence in the green downward version. The biosensor was used to measure cAMP levels in individual human airway smooth muscle (HASM) cells monitored under a fluorescent microscope. The green downward biosensor displayed similar responses to populations of cells when stimulated with forskolin or isoproterenol. This single-cell assay allows visualization of the biosensor location at 20x and 40x magnification. Thus, this cAMP biosensor is sensitive and flexible, allowing real-time measurement of cAMP in both immortalized and primary cells, and with single cells or populations of cells. These attributes make cADDis a valuable tool for studying cAMP signaling dynamics in living cells.
Adenosine 3′,5′-cyclic monophosphate, cAMP, plays a central role in cellular communication and the coordination of various physiological processes. cAMP acts as a second messenger, relaying external signals from hormones, neurotransmitters, or other extracellular molecules to initiate a cascade of intracellular events1. Moreover, cAMP is intricately involved in various signaling pathways, including those associated with G-protein-coupled receptors (GPCRs) and adenylyl cyclases. Understanding the role of cAMP in cellular signaling is fundamental to unraveling the complex mechanisms that underlie normal cellular functions and the deve....
The details of all the reagents and equipment used for the study are listed in the Table of Materials.
1. Plate reading spectrophotometer high-throughput assay
The present study validated the cytosolic biosensor in both plate reader and microscope assays. Once cells expressed the biosensor, they were stimulated with either 10 µM forskolin (a direct activator of adenylyl cyclase), 10 nM isoproterenol (an agonist at ß1AR and ß2AR), or vehicle (Figure 1). The subsequent changes in fluorescence, indicative of cAMP production, were captured every 30 s.
The data was transformed as the chang.......
Accurate and sensitive measurement of cAMP is crucial for understanding its role in various cellular processes and for studying the activity of cAMP-dependent signaling pathways. There are several methods commonly employed to measure cAMP levels, including ELISA, radioimmunoassay, FRET biosensors, and the GloSensor cAMP assay14,15,16,17,18. Each cAMP assay has.......
This study was supported by the National Heart, Lung, and Blood Institute (NHLBI) (HL169522).
....Name | Company | Catalog Number | Comments |
96-well plate (clear) | Fisherbrand | 21-377-203 | |
35 mm dish | Greiner Bio-One | 627870 | Cell culture dishes with glass bottom |
96-well plate | Corning | 3904 | Black with clear flat bottom |
Antibiotic-Antimycotic (100x) | Gibco | 15240062 | For HEK and HASM media |
BZ-X fluorescence microscope | Keyence | ||
Calcium chloride (IM) | Quality Biological Inc | E506 | For HASM media |
Centrifuge tube (15 mL) | Thermo Scientific | 339651 | |
DMEM (1x) | Gibco | 11965092 | HEK media |
DPBS with Mg2+ and Ca2+ | Gibco | 14040-133 | |
DPBS without Mg2+ and Ca2+ | Corning | 14040-133 | |
Fetal Bovine Serum (FBS) | R&D systems | S11195 | For HEK and HASM media |
Forskolin | Millipore | 344270 | Drug |
Green Down cADDis cAMP Assay Kit | Montana Molecular | #D0200G | Reagent |
Ham's F-12K | Gibco | 21127022 | For HASM media |
HEPES (1M) | Gibco | 15630080 | For HASM media |
Isoproterenol | Sigma | I6504 | Drug |
L-glutamine 200 mM (100x) | Gibco | 25030-081 | For HASM media |
Microcentrifuge tube (2 mL) | Eppendorf | 22363352 | |
Primocin | Invitrogen | ant-pm-1 | Antibiotic for HASM media |
RNAse away | Thermo Scientific | 700511 | Reagent |
Sodium hydroxide solution | Sigma | S2770 | For HASM media |
Spectrmax M5 plate reader | Molecular Devices | ||
Trichostatin A | TCI America | T2477 | Reagent |
Trypsin EDTA | Gibco | 25200-056 | Reagent |
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2024 MyJoVE Corporation. All rights reserved