High-throughput microfluidic micropipette aspiration device to probe time-scale dependent nuclear mechanics in intact cells
Year: 2019
Type: article
Abstract: The mechanical properties of the cell nucleus are increasingly recognized as critical in many biological processes. The deformability of the nucleus determines the ability of immune and cancer cells to migrate through tissues and across endothelial cell layers, and changes to the mechanical properties of the nucleus can serve as novel biomarkers in processes such as cancer progression and stem cell differentiation. However, current techniques to measure the viscoelastic nuclear mechanical properties are often time consuming, limited to probing one cell at a time, or require expensive, highly specialized equipment. Furthermore, many current assays do not measure time-dependent properties, which are characteristic of viscoelastic materials. Here, we present an easy-to-use microfluidic device that applies the well-established approach of micropipette aspiration, adapted to measure many cells in parallel. The device design allows rapid loading and purging of cells for measurements, and minimizes clogging by large particles or clusters of cells. Combined with a semi-automated image analysis pipeline, the microfluidic device approach enables significantly increased experimental throughput. We validated the experimental platform by comparing computational models of the fluid mechanics in the device with experimental measurements of fluid flow. In addition, we conducted experiments on cells lacking the nuclear envelope protein lamin A/C and wild-type controls, which have well-characterized nuclear mechanical properties. Fitting time-dependent nuclear deformation data to power law and different viscoelastic models revealed that loss of lamin A/C significantly altered the elastic and viscous properties of the nucleus, resulting in substantially increased nuclear deformability. Lastly, to demonstrate the versatility of the devices, we characterized the viscoelastic nuclear mechanical properties in a variety of cell lines and experimental model systems, including human skin fibroblasts from an individual with a mutation in the lamin gene associated with dilated cardiomyopathy, healthy control fibroblasts, induced pluripotent stem cells (iPSCs), and human tumor cells. Taken together, these experiments demonstrate the ability of the microfluidic device and automated image analysis platform to provide robust, high throughput measurements of nuclear mechanical properties, including time-dependent elastic and viscous behavior, in a broad range of applications.
Source: Lab on a Chip
DOI: 10.1039/c9lc00444k
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Funders: National Science Foundation, U.S. Department of Defense, Fondation ARC pour la Recherche sur le Cancer, Ligue Contre le Cancer, Université Paris-Saclay, National Institutes of Health, National Heart, Lung, and Blood Institute, National Cancer Institute, Division of Chemical, Bioengineering, Environmental, and Transport Systems, Division of Molecular and Cellular Biosciences, Congressionally Directed Medical Research Programs
Awards: G1295293865, CAREER:The role of nuclear biomechanics during cell migration in 3-D environments, G1860755807, G2696452819, G4280930750, Nuclear mechanics and mechanotransduction in muscular laminopathies, G4715424683, G4973925331, G6264665380, NNCI: Cornell Nanoscale Science and Technology Facility (CNF), NSF/MCB-BSF: DYNAMIC MEASUREMENTS OF NUCLEAR MECHANOTRANSDUCTION IN SKELETAL MUSCLE CELLS IN VITRO AND IN VIVO, G7211783408, G9000055822, G9000178996, G985764062
OpenAlex ID: W2972250307
