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Azobenzene-based sinusoidal surface topography drives focal adhesion confinement and guides collective migration of epithelial cells

Tutkimustuotos: ArtikkeliTieteellinenvertaisarvioitu

31 Sitaatiot (Scopus)
60 Lataukset (Pure)

Abstrakti

Surface topography is a key parameter in regulating the morphology and behavior of single cells. At multicellular level, coordinated cell displacements drive many biological events such as embryonic morphogenesis. However, the effect of surface topography on collective migration of epithelium has not been studied in detail. Mastering the connection between surface features and collective cellular behaviour is highly important for novel approaches in tissue engineering and repair. Herein, we used photopatterned microtopographies on azobenzene-containing materials and showed that smooth topographical cues with proper period and orientation can efficiently orchestrate cell alignment in growing epithelium. Furthermore, the experimental system allowed us to investigate how the orientation of the topographical features can alter the speed of wound closure in vitro. Our findings indicate that the extracellular microenvironment topography coordinates their focal adhesion distribution and alignment. These topographic cues are able to guide the collective migration of multicellular systems, even when cell–cell junctions are disrupted.

AlkuperäiskieliEnglanti
Artikkeli15329
Sivumäärä15
JulkaisuScientific Reports
Vuosikerta10
Numero1
DOI - pysyväislinkit
TilaJulkaistu - 2020
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Rahoitus

This project was supported by Emil Aaltonen Foundation and Finnish Cultural Foundation, whom we would like to gratefully acknowledge. A.P., T.O.I. and S.N. are also thankful to the Academy of Finland (Decision numbers 277091, 312628, 287287, 319257, 326362 and 308315) for funding our research. D.A.F. was supported by a grant from the NIH (R01GM114344). B.B. was supported by the NIH Ruth L. Kirschstein NRSA fellowship from the NIH (1F32GM115091). T.H-I was supported by an NSF-GRFP fellowship, Berkeley Stem Cell Center’s NIH Stem Cell Biological Engineering Training Program (T32GM098218), and as a UC Berkeley Lloyd Scholar. D.A.F. is a Chan Zuckerberg Biohub Investigator. The authors acknowledge the Biocenter Finland (BF) and Tampere Imaging Facility (TIF) for their services. We are thankful to Mrs. Julia Johansson for her help during cell culture and Ms. Outi Paloheimo is acknowledged for her assistance in migration experiments. Dr. Matti Virkki is acknowledged for his support in interference lithography. Dr. Donato di Vito is acknowledged for the fruitful discussions on quantitative analyses. We are thankful to Dr. Jonathan Moffat (Oxford Instruments Asylum research) for his valuable contribution in performing AFM analysis on collagen coated substrates. Ms. Maiju Juusela is acknowledged for her assistance in Park system AFM imaging. This work is part of the Academy of Finland Flagship Programme, Photonics Research and Innovation (PREIN, Decision number 320165).

Julkaisufoorumi-taso

  • Jufo-taso 1

!!ASJC Scopus subject areas

  • General

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