4.6 Article

Effect of Geometric Curvature on Collective Cell Migration in Tortuous Microchannel Devices

期刊

MICROMACHINES
卷 11, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/mi11070659

关键词

collective cell migration; tortuous microchannel devices; engineered tissue-scaffold

资金

  1. Japan Society for the Promotion of Science (JSPS) Bilateral Joint Research Project (Japan-Korea) [16032211-000370]
  2. KAKENHI [18H03508]
  3. Fostering Joint International Research [19KK0276]
  4. Grants-in-Aid for Scientific Research [18H03508] Funding Source: KAKEN

向作者/读者索取更多资源

Collective cell migration is an essential phenomenon in many naturally occurring pathophysiological processes, as well as in tissue engineering applications. Cells in tissues and organs are known to sense chemical and mechanical signals from the microenvironment and collectively respond to these signals. For the last few decades, the effects of chemical signals such as growth factors and therapeutic agents on collective cell behaviors in the context of tissue engineering have been extensively studied, whereas those of the mechanical cues have only recently been investigated. The mechanical signals can be presented to the constituent cells in different forms, including topography, substrate stiffness, and geometrical constraint. With the recent advancement in microfabrication technology, researchers have gained the ability to manipulate the geometrical constraints by creating 3D structures to mimic the tissue microenvironment. In this study, we simulate the pore curvature as presented to the cells within 3D-engineered tissue-scaffolds by developing a device that features tortuous microchannels with geometric variations. We show that both cells at the front and rear respond to the varying radii of curvature and channel amplitude by altering the collective migratory behavior, including cell velocity, morphology, and turning angle. These findings provide insights into adaptive migration modes of collective cells to better understand the underlying mechanism of cell migration for optimization of the engineered tissue-scaffold design.

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