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Updated: Dec 26, 2025

A Simplified System for Evaluating Cell Mechanosensing and Durotaxis In Vitro
Published on: August 27, 2015
Scaling up single-cell mechanics to multicellular tissues - the role of the intermediate filament-desmosome network
Joshua A Broussard1,2,3, Avinash Jaiganesh2, Hoda Zarkoob2
1Departments of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA kgreen@northwestern.edu joshua.broussard@northwestern.edu.
Abstract:
Cells and tissues sense, respond to and translate mechanical forces into biochemical signals through mechanotransduction, which governs individual cell responses that drive gene expression, metabolic pathways and cell motility, and determines how cells work together in tissues. Mechanotransduction often depends on cytoskeletal networks and their attachment sites that physically couple cells to each other and to the extracellular matrix. One way that cells associate with each other is through Ca2+-dependent adhesion molecules called cadherins, which mediate cell-cell interactions through adherens junctions, thereby anchoring and organizing the cortical actin cytoskeleton. This actin-based network confers dynamic properties to cell sheets and developing organisms. However, these contractile networks do not work alone but in concert with other cytoarchitectural elements, including a diverse network of intermediate filaments. This Review takes a close look at the intermediate filament network and its associated intercellular junctions, desmosomes. We provide evidence that this system not only ensures tissue integrity, but also cooperates with other networks to create more complex tissues with emerging properties in sensing and responding to increasingly stressful environments. We will also draw attention to how defects in intermediate filament and desmosome networks result in both chronic and acquired diseases.
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