Adenocarcinoma cell mechanobiology is altered by the loss modulus of the surrounding extracellular matrix
Elastic and viscoelastic properties of extracellular matrices (ECM) are known to regulate cellular behavior and mechanosensation differently, with implications for morphogenesis, wound healing, and pathophysiology. Most in vitro cellular processes, including cell migration, are studied on linear-elastic substrates to mimic extracellular matrices. However, most tissues are viscoelastic and display a loss modulus (G) that may be 10-20% of their storage modulus (G) under biophysically relevant conditions. Recent research has shown that cells can distinguish between elastic and viscoelastic ECM, leading to alterations in their cellular morphology, migration rates, and contractility. Here, we present a protocol for creating PAH-based model ECMs that enables the fabrication of viscoelastic substrates with storage moduli similar to those of their elastic counterparts. To explore how G influences epithelial cell mechanobiology, we fabricated tunable viscoelastic model ECMs with G of 3 kPa, 8 kPa, and 12 kPa, and for each, independently tuned G values to approximately 300 Pa, 500 Pa, and 700 Pa, respectively. We found that A549 cells cultured on stiff elastic model ECMs migrated [~]30% slower and formed larger focal adhesions compared to their viscoelastic counterparts. Conversely, A549 cells on intermediate viscoelastic model ECMs exhibited a [~]54% reduction in migration speed, with no significant difference in focal adhesion size relative to their elastic counterparts. These findings highlight the complex interplay between substrate (ECM) elastic and viscoelastic properties in regulating epithelial cell mechanobiology and emphasize the importance of time-dependent matrix mechanics in governing epithelial responses.