4.8 Article

Controlled surface topography regulates collective 3D migration by epithelial-mesenchymal composite embryonic tissues

期刊

BIOMATERIALS
卷 58, 期 -, 页码 1-9

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.04.021

关键词

Morphogenesis; Microstructure; Soft tissue biomechanics; Cell mechanics; Topology

资金

  1. National Institutes of Health [R01 HD044750]
  2. National Science Foundation [CAREER IOS-0845775, CMMI-1100515, CMMI-1100430, CMMI-0856187, CMMI-1160840]
  3. AFOSR [FA9550-13-1-0108]
  4. Direct For Biological Sciences
  5. Division Of Integrative Organismal Systems [0845775] Funding Source: National Science Foundation
  6. Div Of Civil, Mechanical, & Manufact Inn
  7. Directorate For Engineering [1100515] Funding Source: National Science Foundation

向作者/读者索取更多资源

Cells in tissues encounter a range of physical cues as they migrate. Probing single cell and collective migratory responses to physically defined three-dimensional (3D) microenvironments and the factors that modulate those responses are critical to understanding how tissue migration is regulated during development, regeneration, and cancer. One key physical factor that regulates cell migration is topography. Most studies on surface topography and cell mechanics have been carried out with single migratory cells, yet little is known about the spreading and motility response of 3D complex multicellular tissues to topographical cues. Here, we examine the response to complex topographical cues of microsurgically isolated tissue explants composed of epithelial and mesenchymal cell layers from naturally 3D organized embryos of the aquatic frog Xenopus laevis. We control topography using fabricated micropost arrays (MPAs) and investigate the collective 3D migration of these multi-cellular systems in these MPAs. We find that the topography regulates both collective and individual cell migration and that dense MPAs reduce but do not eliminate tissue spreading. By modulating cell size through the cell cycle inhibitor Mitomycin C or the spacing of the MPAs we uncover how 3D topographical cues disrupt collective cell migration. We find surface topography can direct both single cell motility and tissue spreading, altering tissue-scale processes that enable efficient conversion of single cell motility into collective movement. (C) 2015 Elsevier Ltd. All rights reserved.

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