Directed persistent motion maintains sheet integrity during multi-cellular spreading and migration
Source abstract
Abstract
Multi-cellular migration plays an important role in physiological processes such as embryogenesis, cancer metastasis and tissue repair. Collective cell migration involves specific single cell motility behaviour that maintains the integrity of the monolayer and the fluid-like behavior of the sheet at long time scales. We have studied the dynamics of MCF-10A, MDA-MB-231 epithelial cell monolayers and that of a NIH-3t3 fibroblast monolayer. For the case where MCF-10A cell–cell interactions are so weak that single cells can detach from the monolayer, a collective cell front can be maintained by interplay between the directed persistent motion of the monolayer and the random motion of escaping single cells. The dynamics of the MCF-10A monolayer is contrasted with the MDA-MB-231 monolayer where single cells did not detach, with non-interacting NIH-3t3 fibroblast cells that are always random walkers, and with a MCF-10A monolayer treated with a calcium chelating agent that reduces intercellular interactions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Cellular Mechanics and Interactions · Microtubule and mitosis dynamics · 3D Printing in Biomedical Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (48)
Show source-provided references
1. Lauffenburger · Cell · 1996 · 84 · 35910.1016/S0092-8674(00)81280-5 ↗
2. Selmeczi · Biophys. J. · 2005 · 89 · 91210.1529/biophysj.105.061150 ↗
3. Betz · Biophys. J. · 2009 · 96 · 513010.1016/j.bpj.2009.03.045 ↗
4. Knorr · Soft Matter · 2011 · 7 · 319210.1039/c0sm01028f ↗
5. Friedl · Curr. Opin. Cell Biol. · 2004 · 16 · 1410.1016/j.ceb.2003.11.001 ↗
6. Friedl · Nat. Rev. Mol. Cell Biol. · 2009 · 10 · 44510.1038/nrm2720 ↗
7. Wolf · Nat. Cell Biol. · 2007 · 9 · 89310.1038/ncb1616 ↗
8. Alexander · Histochem. Cell Biol. · 2008 · 130 · 114710.1007/s00418-008-0529-1 ↗
9. Dieterich · Proc. Natl. Acad. Sci. U. S. A. · 2008 · 105 · 45910.1073/pnas.0707603105 ↗
10. Poujade · Proc. Natl. Acad. Sci. U. S. A. · 2007 · 104 · 1598810.1073/pnas.0705062104 ↗
11. Vitorino · Genes Dev. · 2008 · 22 · 326810.1101/gad.1725808 ↗
12. Szabo · Phys. Biol. · 2010 · 7 · 04600710.1088/1478-3975/7/4/046007 ↗
13. Ridley · Science · 2003 · 302 · 170410.1126/science.1092053 ↗
14. Czirók · Phys. Rev. Lett. · 1998 · 81 · 303810.1103/PhysRevLett.81.3038 ↗
15. Takagi · PLoS One · 2008 · 3 · e264810.1371/journal.pone.0002648 ↗
16. Mattila · Nat. Rev. Mol. Cell Biol. · 2008 · 9 · 44610.1038/nrm2406 ↗
17. Zimmermann · Biophys. J. · 2012 · 102 · 28710.1016/j.bpj.2011.12.023 ↗
18. Chen · Science · 1997 · 276 · 142510.1126/science.276.5317.1425 ↗
19. Nobes · J. Cell Biol. · 1999 · 144 · 123510.1083/jcb.144.6.1235 ↗
20. Omelchenko · Proc. Natl. Acad. Sci. U. S. A. · 2003 · 100 · 1078810.1073/pnas.1834401100 ↗
21. Angelini · Phys. Rev. Lett. · 2010 · 10410.1103/PhysRevLett.104.168104 ↗
22. Khalil · Integr. Biol. · 2010 · 2 · 56810.1039/c0ib00052c ↗
23. Yin · J. Cell Sci. · 2007 · 120 · 81510.1242/jcs.03389 ↗
24. Fenteany · Curr. Biol. · 2000 · 10 · 83110.1016/S0960-9822(00)00579-0 ↗
25. Farooqui · J. Cell Sci. · 2005 · 118 · 5110.1242/jcs.01577 ↗
26. Nikolic · Am. J. Physiol.: Cell Physiol. · 2006 · 291 · C6810.1152/ajpcell.00411.2005 ↗
27. Nie · Biomaterials · 2007 · 28 · 401710.1016/j.biomaterials.2007.05.037 ↗
28. van der Meer · Am. J. Physiol.: Heart Circ. Physiol. · 2010 · 298 · H71910.1152/ajpheart.00933.2009 ↗
29. Murrell · Pos ONE · 2011 · 6 · e2483
30. Trepat · Nat. Phys. · 2009 · 5 · 42610.1038/nphys1269 ↗
31. Vitorino · Mol. Cell. Biol. · 2010 · 31 · 34210.1128/MCB.00800-10 ↗
32. Petitjean · Biophys. J. · 2010 · 98 · 179010.1016/j.bpj.2010.01.030 ↗
33. Martin · Mol. Cell. Biol. · 2001 · 21 · 652910.1128/MCB.21.19.6529-6536.2001 ↗
34. Balzer · Breast Cancer Res. Treat. · 2010 · 121 · 6510.1007/s10549-009-0457-3 ↗
35. Green · Am. J. Physiol.: Cell Physiol. · 2004 · 287 · C37310.1152/ajpcell.00509.2003 ↗
36. Szabó · Phys. Rev. E: Stat., Nonlinear, Soft Matter Phys. · 2006 · 74 · 06190810.1103/PhysRevE.74.061908 ↗
37. Sommers · Breast Cancer Res. Treat. · 1994 · 31 · 32510.1007/BF00666165 ↗
38. Nieman · J. Cell Biol. · 1999 · 147 · 63110.1083/jcb.147.3.631 ↗
39. Mierke · J. Cell Sci. · 2010 · 124 · 36910.1242/jcs.071985 ↗
40. Li · PLoS One · 2008 · 3 · e209310.1371/journal.pone.0002093 ↗
41. Gov · Proc. Natl. Acad. Sci. U. S. A. · 2007 · 104 · 1597010.1073/pnas.0708037104 ↗
42. Omelchenko · Proc. Natl. Acad. Sci. U. S. A. · 2003 · 100 · 1078810.1073/pnas.1834401100 ↗
43. Dobereiner · Phys. Rev. Lett. · 2004 · 93 · 10810510.1103/PhysRevLett.93.108105 ↗
44. Dubin-Thaler · Biophys. J. · 2004 · 86 · 179410.1016/S0006-3495(04)74246-0 ↗
45. Cuvelier · Curr. Biol. · 2007 · 17 · 69410.1016/j.cub.2007.02.058 ↗
46. Foty · Int. J. Dev. Biol. · 2004 · 48 · 39710.1387/ijdb.041810rf ↗
47. Bindschadler · J. Cell Sci. · 2007 · 120 · 87610.1242/jcs.03395 ↗
48. Tambe · Nat. Mater. · 2011 · 10 · 46910.1038/nmat3025 ↗