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Biology subjects

Conboy, J. P.

Publications and source records attributed to Conboy, J. P..

5 recordsLinked to original sources

Plectin affects cell viscoelasticity at small and large deformations

Plectin is a giant protein of the plakin family that crosslinks the cytoskeleton of mammalian cells. It is expressed in virtually all tissues and its dysfunction is associated with various diseases such as skin blistering. There is evidence that plectin regulates the mechanical integrity of the cytoskeleton in diverse cell and tissue types. However, it is unknown how plectin modulates the mechanical response of cells depending on the frequency and amplitude of mechanical loading. Here we demonstrate the role of plectin in the viscoelastic properties of fibroblasts at small and large deformations by quantitative single-cell compression measurements. To identify the importance of plectin, we compared the mechanical properties of wild type (Plec+/+) fibroblasts and plectin knockout (Plec-/-) fibroblasts. We show that plectin knockout cells are nearly 2-fold softer than wild type cells, but their strain-stiffening behaviour is similar. Plectin deficiency also caused faster viscoelastic stress relaxation at long times. Fluorescence recovery after photobleaching experiments indicated that this was due to 3-fold faster actin turnover. Short-time poroelastic relaxation was also faster in Plec-/- cells as compared to Plec+/+ cells, suggesting a more sparse cytoskeletal network. Confocal imaging indicated that this was due to a marked change in the architecture of the vimentin network, from a fine meshwork in wild type cells to a bundled network in the plectin knockout cells. Our findings therefore indicate that plectin is an important regulator of the organization and viscoelastic properties of the cytoskeleton in fibroblasts. Our findings emphasize that mechanical integration of the different cytoskeletal networks present in cells is important for regulating the versatile mechanical properties of cells. SIGNIFICANCEMammalian cells combine superior mechanical strength with the ability to actively deform themselves. They owe this paradoxical mechanical behaviour to their cytoskeleton, an intracellular web of protein filaments that includes actin filaments and intermediate filaments. It is known that both cytoskeletal filament types contribute to cell stiffness on their own, but the impact of their mechanical integration via cytoskeletal crosslinker proteins remains unknown. Here we test the effect of crosslinking of actin and vimentin intermediate filaments by the crosslinker protein plectin in fibroblasts by single-cell compression measurements. By comparing normal cells and cells in which plectin is knocked out, we find that plectin significantly increases cell stiffness and provides a protective mechanism against actin network disruption by compressive loading.

biophysics↗

Cancer cell deformability impacts the rate of confined migration but not decision making

Cancer cells can utilize different invasion strategies to overcome physical arrest during confined migration through tissues with small pores. Cancer cell plasticity allows switches between different migration modes and transitions between single-cell and collective migration. The biophysical parameters that guide these decisions are poorly understood. In this work we investigated the link between cell deformability and migration efficacy in constrictions of two mesenchymal cancer cell types with similar invasion strategies: HT1080 fibrosarcoma cells and MV3 melanoma cells. To this end, we designed microfluidic platforms for (1) high-throughput cell deformability measurements and (2) migration through a variety of confining geometries. We measured different deformabilities for HT1080 and MV3 cells and correlated this to their migration efficacy through confinements. However, higher deformability and improved squeezing ability did not impact decision-making at junctions of channels of different widths. Our findings show that cell deformability correlates with better squeezing abilities through confinements, but does not impact directionality decisions.

cancer biology↗

Actin and vimentin jointly control cell viscoelasticity and compression stiffening

AbstractThe mechanical properties of cells are governed by the cytoskeleton, a dynamic network of actin filaments, intermediate filaments, and microtubules. Understanding the individual and collective mechanical contributions of these three different cytoskeletal elements is essential to elucidate how cells maintain mechanical integrity during deformation. Here we use a custom single-cell rheometer to identify the distinct contributions of actin and vimentin to the viscoelastic and nonlinear elastic response of cells to uniaxial compression. We used mouse embryonic fibroblasts (MEFs) isolated from wild type (WT) and vimentin knockout (vim -/-) mice in combination with chemical treatments to manipulate actin polymerization and contractility. We show through small amplitude oscillatory measurements and strain ramp tests that vimentin, often overlooked in cellular mechanics, plays a role comparable to actin in maintaining cell stiffness and resisting large compressive forces. However, actin appears to be more important than vimentin in determining cellular energy dissipation. Finally we show by comparing wild type and enucleated cells that compression stiffening originates from the actin and vimentin cytoskeleton, while the nucleus appears to play little role in this. Our findings provide insight into how cytoskeletal networks collectively determine the mechanical properties of cells, providing a basis to understand the role of the cytoskeleton in the ability of cells to resist external as well as internal forces. Significance statementO_LIA cells response to mechanical stress is largely governed by the actin and vimentin cytoskeletal networks, but their relative contribution to cell viscoelasticity and response to large deformations are poorly characterized. C_LIO_LIWe reveal that actin and vimentin networks have an almost equal contribution to cellular stiffness and the cells ability to strain-stiffen under uniaxial compression. C_LIO_LIThis work underscores the cytoskeletons central role in cellular mechanics and the mechanical synergy between the cytoskeletal networks, providing a framework for understanding how cellular components coordinate to maintain structural integrity and respond to different mechanical environments. C_LI

biophysics↗

Optogenetic and chemical genetic tools for rapid repositioning of vimentin intermediate filaments

Intermediate filaments (IFs) are a key component of the cytoskeleton, essential for regulating cell mechanics, maintaining nuclear integrity, organelle positioning, and modulating cell signaling. Current insights into IF function primarily come from studies using long-term perturbations, such as protein depletion or mutation. Here, we present tools that allow rapid manipulation of vimentin IFs in the whole cytoplasm or within specific subcellular regions by inducibly coupling them to microtubule motors, either pharmacologically or using light. Rapid perinuclear clustering of vimentin had no major immediate effects on the actin or microtubule organization, cell spreading, or focal adhesion number, but reduced cell stiffness. Mitochondria and endoplasmic reticulum sheets were reorganized due to vimentin clustering, whereas lysosomes were only briefly displaced and rapidly regained their normal distribution. Keratin moved along with vimentin in some cell lines but remained intact in others. Our tools help to study the immediate and local effects of vimentin perturbation and identify direct links of vimentin to other cellular structures.

cell biology↗

Characterizing microbubble-mediated permeabilization in a vessel-on-a-chip model

Drug transport from blood to extravascular tissue can locally be achieved by increasing the vascular permeability through ultrasound-activated microbubbles. However, the mechanism remains unknown, including whether short and long cycles of ultrasound induce the same onset rate, spatial distribution, and amount of vascular permeability increase. Accurate models are necessary for insights into the mechanism so a microvessel-on-a-chip is developed with a membrane-free extravascular space. Using these microvessels-on-a-chip, we show distinct differences between 2 MHz ultrasound treatments with 10 or 1000 cycles. The onset rate is slower for 10 than 1000 cycles, while both cycle lengths increase the permeability in spot-wise patterns without affecting cell viability. Significantly less vascular permeability increase and sonoporation are induced for 10 versus 1000 cycles at 750 kPa (i.e., highest studied peak negative acoustic pressure (PNP)). The PNP threshold for vascular permeability increases is 750 versus 550 kPa for 10 versus 1000 cycles, while this is 750 versus 220 kPa for sonoporation. Vascular permeability increases do not correlate with v{beta}3-targeted microbubble behavior, while sonoporation correlates with v{beta}3-targeted microbubble clustering. In conclusion, the further mechanistic unraveling of vascular permeability increase by ultrasound-activated microbubbles in a developed microvessel-on-a-chip model aids safe and efficient development of microbubble-mediated drug transport.

bioengineering↗