Dynamic Stress Fiber Reorganization on Stretched Matrices

2014 ◽  
pp. 166-189 ◽  
Keyword(s):  
Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5281
Author(s):  
Mateusz Kozioł ◽  
Piotr Szperlich ◽  
Bartłomiej Toroń ◽  
Piotr Olesik ◽  
Marcin Jesionek

This paper shows a piezoelectric response from an innovative sensor obtained by casting epoxy-SbSI (antimony sulfoiodide) nanowires nanocomposite to a grid structure printed using a fuse deposition modeling (FDM) method. The grid is shown to be a support structure for the nanocomposite. The applied design approach prospectively enables the formation of sensors with a wide spectrum of shapes and a wide applicability. The voltage signal obtained as a result of the piezoelectric effect reached 1.5V and 0.5V under a maximum static stress of 8.5 MPa and under a maximum dynamic stress of 22.3 kPa, respectively. These values are sufficient for potential application in sensor systems. The effect of a systematic increase in the voltage signal with subsequent cycles was also observed, which similarly allows the use of these sensors in monitoring systems for structures exposed to unfavorable cyclical loads. The obtained results also show that the piezoelectric signal improves with increase in strain rate.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Cécile Gaston ◽  
Simon De Beco ◽  
Bryant Doss ◽  
Meng Pan ◽  
Estelle Gauquelin ◽  
...  

AbstractAt the basis of cell shape and behavior, the organization of actomyosin and its ability to generate forces are widely studied. However, the precise regulation of this contractile network in space and time is unclear. Here, we study the role of the epithelial-specific protein EpCAM, a contractility modulator, in cell shape and motility. We show that EpCAM is required for stress fiber generation and front-rear polarity acquisition at the single cell level. In fact, EpCAM participates in the remodeling of a transient zone of active RhoA at the cortex of spreading epithelial cells. EpCAM and RhoA route together through the Rab35/EHD1 fast recycling pathway. This endosomal pathway spatially organizes GTP-RhoA to fine tune the activity of actomyosin resulting in polarized cell shape and development of intracellular stiffness and traction forces. Impairment of GTP-RhoA endosomal trafficking either by silencing EpCAM or by expressing Rab35/EHD1 mutants prevents proper myosin-II activity, stress fiber formation and ultimately cell polarization. Collectively, this work shows that the coupling between co-trafficking of EpCAM and RhoA, and actomyosin rearrangement is pivotal for cell spreading, and advances our understanding of how biochemical and mechanical properties promote cell plasticity.


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