scholarly journals Optogenetic control of intracellular flows and cell migration: A comprehensive mathematical analysis with a minimal active gel model

2021 ◽  
Vol 104 (2) ◽  
Author(s):  
Oliver M. Drozdowski ◽  
Falko Ziebert ◽  
Ulrich S. Schwarz
2014 ◽  
Vol 111 (17) ◽  
pp. 6371-6376 ◽  
Author(s):  
Y. Xu ◽  
Y.-M. Hyun ◽  
K. Lim ◽  
H. Lee ◽  
R. J. Cummings ◽  
...  

Author(s):  
Xenia Meshik ◽  
Patrick R. O’Neill ◽  
N. Gautam

1967 ◽  
Vol 31 ◽  
pp. 313-317 ◽  
Author(s):  
C. C. Lin ◽  
F. H. Shu

Density waves in the nature of those proposed by B. Lindblad are described by detailed mathematical analysis of collective modes in a disk-like stellar system. The treatment is centered around a hypothesis of quasi-stationary spiral structure. We examine (a) the mechanism for the maintenance of this spiral pattern, and (b) its consequences on the observable features of the galaxy.


Author(s):  
J. Roemer ◽  
S.R. Simon

We are developing an in vitro interstitial extracellular matrix (ECM) system for study of inflammatory cell migration. Falcon brand Cyclopore membrane inserts of various pore sizes are used as a support substrate for production of ECM by R22 rat aortic smooth muscle cells. Under specific culture conditions these cells produce a highly insoluble matrix consisting of typical interstitial ECM components, i.e.: types I and III collagen, elastin, proteoglycans and fibronectin.


Author(s):  
Tim Oliver ◽  
Akira Ishihara ◽  
Ken Jacobsen ◽  
Micah Dembo

In order to better understand the distribution of cell traction forces generated by rapidly locomoting cells, we have applied a mathematical analysis to our modified silicone rubber traction assay, based on the plane stress Green’s function of linear elasticity. To achieve this, we made crosslinked silicone rubber films into which we incorporated many more latex beads than previously possible (Figs. 1 and 6), using a modified airbrush. These films could be deformed by fish keratocytes, were virtually drift-free, and showed better than a 90% elastic recovery to micromanipulation (data not shown). Video images of cells locomoting on these films were recorded. From a pair of images representing the undisturbed and stressed states of the film, we recorded the cell’s outline and the associated displacements of bead centroids using Image-1 (Fig. 1). Next, using our own software, a mesh of quadrilaterals was plotted (Fig. 2) to represent the cell outline and to superimpose on the outline a traction density distribution. The net displacement of each bead in the film was calculated from centroid data and displayed with the mesh outline (Fig. 3).


2019 ◽  
Vol 63 (5) ◽  
pp. 579-594 ◽  
Author(s):  
Guillem Lambies ◽  
Antonio García de Herreros ◽  
Víctor M. Díaz

Abstract Cell migration is a multifactorial/multistep process that requires the concerted action of growth and transcriptional factors, motor proteins, extracellular matrix remodeling and proteases. In this review, we focus on the role of transcription factors modulating Epithelial-to-Mesenchymal Transition (EMT-TFs), a fundamental process supporting both physiological and pathological cell migration. These EMT-TFs (Snail1/2, Twist1/2 and Zeb1/2) are labile proteins which should be stabilized to initiate EMT and provide full migratory and invasive properties. We present here a family of enzymes, the deubiquitinases (DUBs) which have a crucial role in counteracting polyubiquitination and proteasomal degradation of EMT-TFs after their induction by TGFβ, inflammatory cytokines and hypoxia. We also describe the DUBs promoting the stabilization of Smads, TGFβ receptors and other key proteins involved in transduction pathways controlling EMT.


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