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  • Stem cell migration and mechanotransduction on linear stiffness gradient hydrogels.

Stem cell migration and mechanotransduction on linear stiffness gradient hydrogels.

Proceedings of the National Academy of Sciences of the United States of America (2017-05-17)
William J Hadden, Jennifer L Young, Andrew W Holle, Meg L McFetridge, Du Yong Kim, Philip Wijesinghe, Hermes Taylor-Weiner, Jessica H Wen, Andrew R Lee, Karen Bieback, Ba-Ngu Vo, David D Sampson, Brendan F Kennedy, Joachim P Spatz, Adam J Engler, Yu Suk Choi
ABSTRACT

The spatial presentation of mechanical information is a key parameter for cell behavior. We have developed a method of polymerization control in which the differential diffusion distance of unreacted cross-linker and monomer into a prepolymerized hydrogel sink results in a tunable stiffness gradient at the cell-matrix interface. This simple, low-cost, robust method was used to produce polyacrylamide hydrogels with stiffness gradients of 0.5, 1.7, 2.9, 4.5, 6.8, and 8.2 kPa/mm, spanning the in vivo physiological and pathological mechanical landscape. Importantly, three of these gradients were found to be nondurotactic for human adipose-derived stem cells (hASCs), allowing the presentation of a continuous range of stiffnesses in a single well without the confounding effect of differential cell migration. Using these nondurotactic gradient gels, stiffness-dependent hASC morphology, migration, and differentiation were studied. Finally, the mechanosensitive proteins YAP, Lamin A/C, Lamin B, MRTF-A, and MRTF-B were analyzed on these gradients, providing higher-resolution data on stiffness-dependent expression and localization.

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Sigma-Aldrich
Monoclonal Anti-MKL2 antibody produced in mouse, Prestige Antibodies® Powered by Atlas Antibodies, clone CL1546, purified immunoglobulin, buffered aqueous glycerol solution