Stem cell migration and mechanotransduction on linear stiffness gradient hydrogels.
William J HaddenJennifer L YoungAndrew W HolleMeg L McFetridgeDu Yong KimPhilip WijesingheHermes Taylor-WeinerJessica H WenAndrew R LeeKaren BiebackBa-Ngu VoDavid D SampsonBrendan F KennedyJoachim P SpatzAdam J EnglerYu Suk ChoiPublished in: Proceedings of the National Academy of Sciences of the United States of America (2017)
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.
Keyphrases
- cell migration
- stem cells
- low cost
- single cell
- drug delivery
- cell therapy
- hyaluronic acid
- endothelial cells
- case report
- tissue engineering
- drug release
- electronic health record
- extracellular matrix
- high resolution
- health information
- induced pluripotent stem cells
- mass spectrometry
- deep learning
- quantum dots
- tandem mass spectrometry