Living Cell Assay

A living cell assay is an experimental method that measures biological responses in viable cells, preserving cellular activity and interactions during analysis. In these assays, researchers expose cells to a compound, stimulus, or environmental condition and quantify changes through readouts such as viability, morphology, signaling, metabolism, or gene expression, using real-time or endpoint measurements. Living cell assays support drug discovery, toxicity testing, disease modeling, and studies of cellular physiology in biology. Because they capture responses in functioning cells rather than isolated molecules, they can reveal dynamic effects and help evaluate how experimental treatments influence cellular behavior.

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JoVE EoE - Neuropathology

Live-cell Phagocytosis Assay of Microglia-Like Cells Using Human Synaptosomes

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2025

Source: Funes, S., et. al., Human Microglia-like Cells: Differentiation from Induced Pluripotent Stem Cells and In Vitro Live-cell Phagocytosis Assay using Human Synaptosomes. J. Vis. Exp. (2022)This video demonstrates an assay to study the phagocytic capacity of microglia-like cells using pH-sensitive fluorescent dye-labeled synaptosomes.

Lipid Exchange Assay in Living Cells

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2025

We describe a method for using cyclodextrin to mediate exchange between lipids of the plasma membrane with exogenous lipids. This technique can be paired with experiments studying transmembrane proteins, which behave differently in lipid raft-like environments than they do in non-raft-like environments.

G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay

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Cited by 4 •

2016

Simple methods to detect the selective activation of G proteins by G protein-coupled receptors remain an outstanding challenge in cell signaling. Here, Fӧrster resonance energy transfer (FRET) biosensors have been developed by pairwise tethering a GPCR to G protein peptides to probe conformational changes at controlled concentrations in live cells.

Live-cell Measurement of Odorant Receptor Activation Using a Real-time cAMP Assay

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Cited by 13 •

2017

Characterizing the function of odorant receptors serves an indispensable part in the deorphanization process. We describe a method to measure the activation of odorant receptors in real time using a cAMP assay.

Assay Development for High Content Quantification of Sod1 Mutant Protein Aggregate Formation in Living Cells

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Cited by 2 •

2017

We describe a method to quantify the aggregation of misfolded proteins. Our protocol details lentiviral induced stable cell line generation, automated confocal imaging, and image analysis of protein aggregates. As an illustrative application, we studied the effect of small molecules in promoting SOD1 aggregation in a time- and dose-dependent manner.

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