Non-dimensional expression of the stiffening response of tensegrity structure as a function of strain: Application to cell mechanics

1998 ◽  
Vol 31 ◽  
pp. 174
Author(s):  
S. Wendling ◽  
C. Oddou ◽  
D. Isabey
1997 ◽  
Vol 64 (3) ◽  
pp. 480-486 ◽  
Author(s):  
M. F. Coughlin ◽  
D. Stamenovic´

A tensegrity structure composed of six slender struts interconnected with 24 linearly elastic cables is used as a model of cell deformability. Struts are allowed to buckle under compression and their post-buckling behavior is determined from an energy formulation of the classical pin-ended Euler column. At the reference state, the cables carry initial tension balanced by forces exerted by struts. The structure is stretched uniaxially and the stretching force versus axial extension relationships are obtained for different initial cable tensions by considering equilibrium at the joints. Structural stiffness is calculated as the ratio of stretching force to axial extension. Predicted dependences of structural stiffness on initial cable tension and on stretching force are consistent with behaviors observed in living cells. These predictions are both qualitatively and quantitatively superior to those obtained previously from the model in which the struts are viewed as rigid.


2006 ◽  
Vol 75 (4-5) ◽  
pp. 289-301 ◽  
Author(s):  
K.A. Lazopoulos ◽  
N.K. Lazopoulou

2006 ◽  
Vol 182 (3-4) ◽  
pp. 253-263 ◽  
Author(s):  
K. A. Lazopoulos ◽  
N. K. Lazopoulou

Cells ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 851
Author(s):  
Veronika Pfannenstill ◽  
Aurélien Barbotin ◽  
Huw Colin-York ◽  
Marco Fritzsche

Mechanobiology seeks to understand how cells integrate their biomechanics into their function and behavior. Unravelling the mechanisms underlying these mechanobiological processes is particularly important for immune cells in the context of the dynamic and complex tissue microenvironment. However, it remains largely unknown how cellular mechanical force generation and mechanical properties are regulated and integrated by immune cells, primarily due to a profound lack of technologies with sufficient sensitivity to quantify immune cell mechanics. In this review, we discuss the biological significance of mechanics for immune cells across length and time scales, and highlight several experimental methodologies for quantifying the mechanics of immune cells. Finally, we discuss the importance of quantifying the appropriate mechanical readout to accelerate insights into the mechanobiology of the immune response.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Christian Aermes ◽  
Alexander Hayn ◽  
Tony Fischer ◽  
Claudia Tanja Mierke

AbstractThe knowledge of cell mechanics is required to understand cellular processes and functions, such as the movement of cells, and the development of tissue engineering in cancer therapy. Cell mechanical properties depend on a variety of factors, such as cellular environments, and may also rely on external factors, such as the ambient temperature. The impact of temperature on cell mechanics is not clearly understood. To explore the effect of temperature on cell mechanics, we employed magnetic tweezers to apply a force of 1 nN to 4.5 µm superparamagnetic beads. The beads were coated with fibronectin and coupled to human epithelial breast cancer cells, in particular MCF-7 and MDA-MB-231 cells. Cells were measured in a temperature range between 25 and 45 °C. The creep response of both cell types followed a weak power law. At all temperatures, the MDA-MB-231 cells were pronouncedly softer compared to the MCF-7 cells, whereas their fluidity was increased. However, with increasing temperature, the cells became significantly softer and more fluid. Since mechanical properties are manifested in the cell’s cytoskeletal structure and the paramagnetic beads are coupled through cell surface receptors linked to cytoskeletal structures, such as actin and myosin filaments as well as microtubules, the cells were probed with pharmacological drugs impacting the actin filament polymerization, such as Latrunculin A, the myosin filaments, such as Blebbistatin, and the microtubules, such as Demecolcine, during the magnetic tweezer measurements in the specific temperature range. Irrespective of pharmacological interventions, the creep response of cells followed a weak power law at all temperatures. Inhibition of the actin polymerization resulted in increased softness in both cell types and decreased fluidity exclusively in MDA-MB-231 cells. Blebbistatin had an effect on the compliance of MDA-MB-231 cells at lower temperatures, which was minor on the compliance MCF-7 cells. Microtubule inhibition affected the fluidity of MCF-7 cells but did not have a significant effect on the compliance of MCF-7 and MDA-MB-231 cells. In summary, with increasing temperature, the cells became significant softer with specific differences between the investigated drugs and cell lines.


Soft Matter ◽  
2021 ◽  
Author(s):  
Iman Elbalasy ◽  
Paul Mollenkopf ◽  
Cary Tutmarc ◽  
Harald Herrmann ◽  
Jörg Schnauß

The cytoskeleton is a major determinant of cell mechanics, and alterations in the central mechanical aspects of cells are observed during many pathological situations. Therefore, it is essential to investigate...


2015 ◽  
Vol 108 (2) ◽  
pp. 142a-143a
Author(s):  
Alexandra Surcel ◽  
Qingfeng Zhu ◽  
Eric Schiffhauer ◽  
Robert Anders ◽  
Douglas Robinson

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