scholarly journals DLITE: Dynamic Local Intercellular Tension Estimation

2019 ◽  
Author(s):  
R. Vasan ◽  
M.M. Maleckar ◽  
C.D. Williams ◽  
P. Rangamani

AbstractThe shape of cell-cell interfaces and the forces resulting from actomyosin interactions, mem-brane tension, or cell-cell adhesion are closely coupled. For example, the tight junction protein, ZO-1, forms a link between the force-bearing actin cortex and the rest of the tight junction protein (TJP) complex, regulating epithelial cell differentiation and the flux of solutes across epithelia. Here we introduce a method for Dynamic Local Intercellular Tension Estimation (DLITE) to computationally infer the evolution of cell-cell forces from a mechanical model of collective cell behaviour. This builds upon prior work in the field (CellFIT, Brodland et al., PloS one 9.6 (2014): e99116). We validate our estimated forces against those predicted by Surface Evolver simulations. Inferred tensions of a cell colony rearranging over time correlate better with the ground truth for our method (DLITE) than for prior methods intended for single time-points. DLITE is robust to both skeletonization errors and topological changes. Finally, we used DLITE in WTC-11 human induced pluripotent stem (hIPS) cells endogenously expressing ZO-1 GFP to find that major topo-logical changes in cell connectivity, e.g. mitosis, can result in an increase in tension. This suggests a correlation between the dynamics of cell-cell forces and colony rearrangement.


2008 ◽  
Vol 182 (6) ◽  
pp. i13-i13
Author(s):  
Ulrike Lisewski ◽  
Yu Shi ◽  
Uta Wrackmeyer ◽  
Robert Fischer ◽  
Chen Chen ◽  
...  


2005 ◽  
Vol 309 (2) ◽  
pp. 345-357 ◽  
Author(s):  
M LADWEIN ◽  
U PAPE ◽  
D SCHMIDT ◽  
M SCHNOLZER ◽  
S FIEDLER ◽  
...  






2010 ◽  
Vol 285 (44) ◽  
pp. 33584-33588 ◽  
Author(s):  
Kerstin Duning ◽  
Deike Rosenbusch ◽  
Marc A. Schlüter ◽  
Yuemin Tian ◽  
Karl Kunzelmann ◽  
...  


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Yi-Fang Tu ◽  
Si-Tse Jiang ◽  
Chi-Wu Chiang ◽  
Li-Ching Chen ◽  
Chao-Ching Huang

AbstractHypoxic-ischemic (HI) encephalopathy is the major cause of mortality and disability in newborns. The neurovascular unit is a major target of acute and chronic brain injury, and therapies that protect simultaneously both neurons and vascular endothelial cells from neonatal HI injury are in demand. Insulin receptors and its key downstream molecule-insulin receptor substrate −1 (IRS-1) are potential neuroprotective targets and expressed both in neuron and endothelial cells. To investigate whether IRS-1 can act similarly in neurons and vascular endothelial cells in protecting neurovascular units and brain form HI injury, we found that neuron-specific IRS-1 transgenic rats showed reduced neurovascular injury and infarct volumes, whereas endothelial-specific IRS-1 transgenic rats showed increased blood-brain barrier (BBB) disruption and exaggerated neurovascular injury after neonatal HI brain injury. Endothelial-specific IRS-1 overexpression increased vascular permeability and disassembled the tight junction protein (zonula occludens-1) complex. Inhibition of mammalian target of rapamycin (mTOR) by rapamycin preserved tight junction proteins and attenuated BBB leakage and neuronal apoptosis after HI in the endothelial-specific IRS-1 transgenic pups. Together, our findings suggested that neuronal and endothelial IRS-1 had opposite effects on the neurovascular integrity and damage after neonatal HI brain injury and that endothelial IRS-1 worsens neurovascular integrity after HI via mTOR-mediated tight junction protein disassembly.



2009 ◽  
Vol 1165 (1) ◽  
pp. 88-98 ◽  
Author(s):  
Sandra Citi ◽  
Serge Paschoud ◽  
Pamela Pulimeno ◽  
Francesco Timolati ◽  
Fabrizio De Robertis ◽  
...  


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