scholarly journals Automated live cell imaging of cell migration across a microfluidic-controlled chemoattractant gradient

2015 ◽  
Vol 12 (11) ◽  
pp. vii-viii ◽  
Author(s):  
Philip Lee ◽  
Cindy S Y Chen ◽  
Terry Gaige ◽  
Paul J Hung
2015 ◽  
Vol 209 (6) ◽  
pp. 803-812 ◽  
Author(s):  
Elizabeth M. Haynes ◽  
Sreeja B. Asokan ◽  
Samantha J. King ◽  
Heath E. Johnson ◽  
Jason M. Haugh ◽  
...  

The lamellipodium is an important structure for cell migration containing branched actin nucleated via the Arp2/3 complex. The formation of branched actin is relatively well studied, but less is known about its disassembly and how this influences migration. GMF is implicated in both Arp2/3 debranching and inhibition of Arp2/3 activation. Modulation of GMFβ, a ubiquitous GMF isoform, by depletion or overexpression resulted in changes in lamellipodial dynamics, branched actin content, and migration. Acute pharmacological inhibition of Arp2/3 by CK-666, coupled to quantitative live-cell imaging of the complex, showed that depletion of GMFβ decreased the rate of branched actin disassembly. These data, along with mutagenesis studies, suggest that debranching (not inhibition of Arp2/3 activation) is a primary activity of GMFβ in vivo. Furthermore, depletion or overexpression of GMFβ disrupted the ability of cells to directionally migrate to a gradient of fibronectin (haptotaxis). These data suggest that debranching by GMFβ plays an important role in branched actin regulation, lamellipodial dynamics, and directional migration.


Author(s):  
Wies van Roosmalen ◽  
Sylvia E. Le Dévédec ◽  
Sandra Zovko ◽  
Hans de Bont ◽  
Bob van de Water

Lab on a Chip ◽  
2016 ◽  
Vol 16 (17) ◽  
pp. 3304-3316 ◽  
Author(s):  
Evelien Mathieu ◽  
Colin D. Paul ◽  
Richard Stahl ◽  
Geert Vanmeerbeeck ◽  
Veerle Reumers ◽  
...  

Lens-free imaging using coherent illumination is established as an inexpensive and reliable alternative to conventional phase contrast microscopy for live-cell imaging applications.


2019 ◽  
Author(s):  
Cara R. Schiavon ◽  
Tong Zhang ◽  
Bing Zhao ◽  
Leonardo Andrade ◽  
Melissa Wu ◽  
...  

AbstractThe actin cytoskeleton plays multiple critical roles in cells, from cell migration to organelle dynamics. The small and transient actin structures regulating organelle dynamics are difficult to detect with fluorescence microscopy. We developed an approach using fluorescent protein-tagged actin nanobodies targeted to organelle membranes to enable live cell imaging of sub-organellar actin dynamics with unprecedented spatiotemporal resolution. These probes reveal that ER-associated actin drives fission of multiple organelles including mitochondria, endosomes, lysosomes, peroxisomes, and the Golgi.


Author(s):  
Jeong-Eun Park ◽  
Su Hoon Lee ◽  
Dong Jun Park ◽  
Young Joon Seo ◽  
Sung Kyun Kim

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