Probing Leader Cells in Endothelial Collective Migration by Plasma Lithography Geometric Confinement

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Yang, Yongliang ^a   Jamilpour, Nima ^a   Yao, Baoyin ^a,b   Dean, Zachary S ^c   Riahi, Reza ^a   Wong, Pak Kin ^a,c,d  

^a University of Arizona   (United States)

^b BEIHANG UNIVERSITY   (China)

^c UNIVERSITY OF ARIZONA   (United States)

^d PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL JUNCTION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MICROSCOPY; PARTICLE IMAGE VELOCIMETRY; PHENOTYPE; PLASMA; STRESS FIBER; VELOCITY; ACTIN FILAMENT; ADHERENS JUNCTION; CELL MOTION; CYTOLOGY; METABOLISM; PHYSIOLOGY; PLASMA GAS; UMBILICAL VEIN ENDOTHELIAL CELL;

PLASMA GAS;

ACTIN CYTOSKELETON; ADHERENS JUNCTIONS; CELL MOVEMENT; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; PLASMA GASES;

EID: 84960193901     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep22707     Document Type: Article

References (31)

1. Cines, D. B. et al. Endothelial cells in physiology and in the pathophysiology of vascular disorders. Blood 91, 3527-3561 (1998).
2. Vitorino, P., Meyer, T. Modular control of endothelial sheet migration. Genes Dev 22, 3268-3281, doi: 10.1101/gad.1725808 (2008).
3. Vitorino, P., Hammer, M., Kim, J., Meyer, T. A steering model of endothelial sheet migration recapitulates monolayer integrity and directed collective migration. Molecular and Cellular Biology 31, 342-350, doi: 10.1128/MCB.00800-10 (2011).
4. Tsai, F. C. et al. A polarized Ca2+, diacylglycerol and STIM1 signalling system regulates directed cell migration. Nature cell biology 16, 133-144, doi: 10.1038/ncb2906 (2014).
5. Omelchenko, T., Vasiliev, J. M., Gelfand, I. M., Feder, H. H., Bonder, E. M. Rho-dependent formation of epithelial "leader" cells during wound healing. Proc Natl Acad Sci USA 100, 10788-10793, doi: 10.1073/pnas.1834401100 (2003).
6. Wynn, M. L., Rupp, P., Trainor, P. A., Schnell, S., Kulesa, P. M. Follow-the-leader cell migration requires biased cell-cell contact and local microenvironmental signals. Physical biology 10, 035003, doi: 10.1088/1478-3975/10/3/035003 (2013).
7. Reffay, M. et al. Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells. Nature cell biology 16, 217-223, doi: 10.1038/ncb2917 (2014).
8. Chapnick, D. A., Liu, X. Leader cell positioning drives wound-directed collective migration in TGFbeta-stimulated epithelial sheets. Molecular biology of the cell 25, 1586-1593, doi: 10.1091/mbc.E14-01-0697 (2014).
9. Rausch, S. et al. Polarizing cytoskeletal tension to induce leader cell formation during collective cell migration. Biointerphases 8, 32, doi: 10.1186/1559-4106-8-32 (2013).
10. Tse, J. M. et al. Mechanical compression drives cancer cells toward invasive phenotype. Proc Natl Acad Sci USA 109, 911-916, doi: 10.1073/pnas.1118910109 (2012).
11. Yamaguchi, N., Mizutani, T., Kawabata, K., Haga, H. Leader cells regulate collective cell migration via Rac activation in the downstream signaling of integrin beta1 and PI3K. Scientific reports 5, 7656, doi: 10.1038/srep07656 (2015).
12. Riahi, R. et al. Notch1-Dll4 signalling and mechanical force regulate leader cell formation during collective cell migration. Nature communications 6, 6556, doi: 10.1038/ncomms7556 (2015).
13. Bi, X., Crum, B. P., Li, W. Super Hydrophobic Parylene-C Produced by Consecutive ${rm O}-{2} $ and ${rm SF}-{6} $ Plasma Treatment. Microelectromechanical Systems, Journal of 23, 628-635 (2014).
14. Junkin, M., Watson, J., Geest, J. P. V., Wong, P. K. Template-guided self-assembly of colloidal quantum dots using plasma lithography. Adv Mater 21, 1247-1251 (2009).
15. Junkin, M., Leung, S. L., Whitman, S., Gregorio, C. C., Wong, P. K. Cellular self-organization by autocatalytic alignment feedback. Journal of cell science 124, 4213-4220, doi: 10.1242/Jcs.088898 (2011).
16. Junkin, M., Wong, P. K. Probing cell migration in confined environments by plasma lithography. Biomaterials 32, 1848-1855, doi: 10.1016/j.biomaterials.2010.11.009 (2011).
17. Yang, Y. L., Volmering, J., Junkin, M., Wong, P. K. Comparative assembly of colloidal quantum dots on surface templates patterned by plasma lithography. Soft Matter 7, 10085-10090, doi: 10.1039/C1sm06142a (2011).
18. Riahi, R., Yang, Y. L., Zhang, D. D., Wong, P. K. Advances in wound-healing assays for probing collective cell migration. J Lab Autom 17, 59-65, doi: 10.1177/2211068211426550 (2012).
19. Junkin, M. et al. Mechanically induced intercellular calcium communication in confined endothelial structures. Biomaterials 34, 2049-2056, doi: 10.1016/j.biomaterials.2012.11.060 (2013).
20. Long, J., Junkin, M., Wong, P. K., Hoying, J., Deymier, P. Calcium Wave Propagation in Networks of Endothelial Cells: Modelbased Theoretical and Experimental Study. Plos Comput Biol 8, e1002847, doi: 10.1371/journal.pcbi.1002847 (2012).
21. Nam, K. H. et al. Probing mechanoregulation of neuronal differentiation by plasma lithography patterned elastomeric substrates. Scientific reports 4, 6965, doi: 10.1038/srep06965 (2014).
22. Block, E. R., Matela, A. R., SundarRaj, N., Iszkula, E. R., Klarlund, J. K. Wounding induces motility in sheets of corneal epithelial cells through loss of spatial constraints: role of heparin-binding epidermal growth factor-like growth factor signaling. The Journal of biological chemistry 279, 24307-24312, doi: 10.1074/jbc.M401058200 (2004).
23. Nikolic, D. L., Boettiger, A. N., Bar-Sagi, D., Carbeck, J. D., Shvartsman, S. Y. Role of boundary conditions in an experimental model of epithelial wound healing. American Journal of Physiology-Cell Physiology 291, C68-C75, doi: 10.1152/ajpcell.00411.2005 (2006).
24. Riahi, R. et al. Single cell gene expression analysis in injury-induced collective cell migration. Integrative biology : quantitative biosciences from nano to macro 6, 192-202, doi: 10.1039/c3ib40095f (2014).
25. Petitjean, L. et al. Velocity fields in a collectively migrating epithelium. Biophysical Journal 98, 1790-1800, doi: 10.1016/j. bpj.2010.01.030 (2010).
26. Cohen, D. J., Nelson, W. J., Maharbiz, M. M. Galvanotactic control of collective cell migration in epithelial monolayers. Nature Materials 13, 409-417, doi: 10.1038/Nmat3891 (2014).
27. Vedula, S. R. et al. Emerging modes of collective cell migration induced by geometrical constraints. Proc Natl Acad Sci USA 109, 12974-12979, doi: 10.1073/pnas.1119313109 (2012).
28. Millan, J. et al. Adherens junctions connect stress fibres between adjacent endothelial cells. Bmc Biol 8, 11, doi: 10.1186/1741-7007-8-11 (2010).
29. Dean, Z. S., Riahi, R., Wong, P. K. Spatiotemporal dynamics of microRNA during epithelial collective cell migration. Biomaterials 37, 156-163 (2015).
30. Huveneers, S. et al. Vinculin associates with endothelial VE-cadherin junctions to control force-dependent remodeling. The Journal of cell biology 196, 641-652, doi: 10.1083/jcb.201108120 (2012).
31. Takeichi, M. Dynamic contacts: rearranging adherens junctions to drive epithelial remodelling. Nature reviews. Molecular cell biology 15, 397-410, doi: 10.1038/nrm3802 (2014).