Integrin α5β1 nano-presentation regulates collective keratinocyte migration independent of substrate rigidity
J. Di Russo, J. L. Young, J. W. R. Wegner, T. Steins, H. Kessler, J. P. Spatz
Abstract
Nanometer-scale properties of the extracellular matrix influence many biological processes, including cell motility. While much information is available for single cell migration, to date, no knowledge exists on how the nanoscale presentation of extracellular matrix receptors influences collective cell migration. In wound healing, basal keratinocytes collectively migrate on a fibronectin-rich provisional basement membrane to re-epithelialize the injured skin. Among other receptors, the fibronectin receptor integrin 5{beta}1 plays a pivotal role in this process. Using a highly specific integrin 5{beta}1 peptidomimetic combined with nanopatterned hydrogels, we show that keratinocyte sheets regulate their migration ability at an optimal integrin 5{beta}1 nanospacing. This efficiency relies on the effective propagation of stresses within the cell monolayer independent of substrate stiffness. For the first time, this work highlights the importance of extracellular matrix receptor nanoscale organization required for efficient tissue regeneration.
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