4.4 Article

Simplified, High-throughput Analysis of Single-cell Contractility using Micropatterned Elastomers

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JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/63211

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  1. UCLA Molecular Shared Screening Resource (MSSR)
  2. Forcyte

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Cellular contractile force is a fundamental trait shared by all cells, and it is crucial for development and function at both cellular and tissue levels. This force also regulates mechanical systems in the body. Various biological processes, including cell motility, adhesion, division, and organ contraction, rely on force. Exaggerated or disrupted cellular contractility can lead to disease processes. This article presents a comprehensive protocol for a microplate-based contractility assay technology called FLECS, which simplifies the analysis of single-cell contractility. This technology allows researchers to study this difficult-to-quantify cell phenotype, effectively lowering the entry barrier into the field of force biology and phenotypic screening of contractile cell force.
Cellular contractile force generation is a fundamental trait shared by virtually all cells. These contractile forces are crucial to proper development, function at both the cellular and tissue levels,and regulate the mechanical systems in the body. Numerous biological processes are force-dependent, including motility, adhesion, and division of single-cells, as well as contraction and relaxation of organs such as the heart, bladder, lungs, intestines, and uterus. Given its importance in maintaining proper physiological function, cellular contractility can also drive disease processes when exaggerated or disrupted. Asthma, hypertension, preterm labor, fibrotic scarring, and underactive bladder are all examples of mechanically driven disease processes that could potentially be alleviated with proper control of cellular contractile force. Here, we present a comprehensive protocol for utilizing a novel microplate-based contractility assay technology known as fluorescently labeled elastomeric contractible surfaces (FLECS), that provides simplified and intuitive analysis of single-cell contractility in a massively scaled manner. Herein, we provide a step-wise protocol for obtaining two six-point dose-response curves describing the effects of two contractile inhibitors on the contraction of primary human bladder smooth muscle cells in a simple procedure utilizing just a single FLECS assay microplate, to demonstrate proper technique to users of the method. Using FLECS Technology, all researchers with basic biological laboratories and fluorescent microscopy systems gain access to studying this fundamental but difficult-to-quantify functional cell phenotype, effectively lowering the entry barrier into the field of force biology and phenotypic screening of contractile cell force.

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