Driving Cells with Light‐Controlled Topographies
Abstract Cell–substrate interactions can modulate cellular behaviors in a variety of biological contexts, including development and disease. Light‐responsive materials have been recently proposed to engineer active substrates with programmable topographies directing cell adhesion, migration, and dif...
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Online Access: | https://doi.org/10.1002/advs.201801826 |
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doaj-c92ad8091b794d5db10329c245c891ce2020-11-25T00:24:50ZengWileyAdvanced Science2198-38442019-07-01614n/an/a10.1002/advs.201801826Driving Cells with Light‐Controlled TopographiesAlberto Puliafito0Serena Ricciardi1Federica Pirani2Viktorie Čermochová3Luca Boarino4Natascia De Leo5Luca Primo6Emiliano Descrovi7Candiolo Cancer Institute FPO‐IRCCS Candiolo Turin 10060 ItalyDepartment of Applied Science and Technology Polytechnic University of Turin C.so Duca degli Abruzzi 24 Turin 10129 ItalyDepartment of Applied Science and Technology Polytechnic University of Turin C.so Duca degli Abruzzi 24 Turin 10129 ItalyDepartment of Applied Science and Technology Polytechnic University of Turin C.so Duca degli Abruzzi 24 Turin 10129 ItalyQuantum Research Labs & Nanofacility Piemonte Nanoscience & Materials Division Istituto Nazionale di Ricerca Metrologica Strada delle Cacce 91 Turin 10135 ItalyQuantum Research Labs & Nanofacility Piemonte Nanoscience & Materials Division Istituto Nazionale di Ricerca Metrologica Strada delle Cacce 91 Turin 10135 ItalyCandiolo Cancer Institute FPO‐IRCCS Candiolo Turin 10060 ItalyDepartment of Applied Science and Technology Polytechnic University of Turin C.so Duca degli Abruzzi 24 Turin 10129 ItalyAbstract Cell–substrate interactions can modulate cellular behaviors in a variety of biological contexts, including development and disease. Light‐responsive materials have been recently proposed to engineer active substrates with programmable topographies directing cell adhesion, migration, and differentiation. However, current approaches are affected by either fabrication complexity, limitations in the extent of mechanical stimuli, lack of full spatio‐temporal control, or ease of use. Here, a platform exploiting light to plastically deform micropatterned polymeric substrates is presented. Topographic changes with remarkable relief depths in the micron range are induced in parallel, by illuminating the sample at once, without using raster scanners. In few tens of seconds, complex topographies are instructed on demand, with arbitrary spatial distributions over a wide range of spatial and temporal scales. Proof‐of‐concept data on breast cancer cells and normal kidney epithelial cells are presented. Both cell types adhere and proliferate on substrates without appreciable cell damage upon light‐induced substrate deformations. User‐provided mechanical stimulation aligns and guides cancer cells along the local deformation direction and constrains epithelial colony growth by biasing cell division orientation. This approach is easy to implement on general‐purpose optical microscopy systems and suitable for use in cell biology in a wide variety of applications.https://doi.org/10.1002/advs.201801826cell‐instructive substratescell migrationcell orientationlight‐responsive polymersoptical manipulation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alberto Puliafito Serena Ricciardi Federica Pirani Viktorie Čermochová Luca Boarino Natascia De Leo Luca Primo Emiliano Descrovi |
spellingShingle |
Alberto Puliafito Serena Ricciardi Federica Pirani Viktorie Čermochová Luca Boarino Natascia De Leo Luca Primo Emiliano Descrovi Driving Cells with Light‐Controlled Topographies Advanced Science cell‐instructive substrates cell migration cell orientation light‐responsive polymers optical manipulation |
author_facet |
Alberto Puliafito Serena Ricciardi Federica Pirani Viktorie Čermochová Luca Boarino Natascia De Leo Luca Primo Emiliano Descrovi |
author_sort |
Alberto Puliafito |
title |
Driving Cells with Light‐Controlled Topographies |
title_short |
Driving Cells with Light‐Controlled Topographies |
title_full |
Driving Cells with Light‐Controlled Topographies |
title_fullStr |
Driving Cells with Light‐Controlled Topographies |
title_full_unstemmed |
Driving Cells with Light‐Controlled Topographies |
title_sort |
driving cells with light‐controlled topographies |
publisher |
Wiley |
series |
Advanced Science |
issn |
2198-3844 |
publishDate |
2019-07-01 |
description |
Abstract Cell–substrate interactions can modulate cellular behaviors in a variety of biological contexts, including development and disease. Light‐responsive materials have been recently proposed to engineer active substrates with programmable topographies directing cell adhesion, migration, and differentiation. However, current approaches are affected by either fabrication complexity, limitations in the extent of mechanical stimuli, lack of full spatio‐temporal control, or ease of use. Here, a platform exploiting light to plastically deform micropatterned polymeric substrates is presented. Topographic changes with remarkable relief depths in the micron range are induced in parallel, by illuminating the sample at once, without using raster scanners. In few tens of seconds, complex topographies are instructed on demand, with arbitrary spatial distributions over a wide range of spatial and temporal scales. Proof‐of‐concept data on breast cancer cells and normal kidney epithelial cells are presented. Both cell types adhere and proliferate on substrates without appreciable cell damage upon light‐induced substrate deformations. User‐provided mechanical stimulation aligns and guides cancer cells along the local deformation direction and constrains epithelial colony growth by biasing cell division orientation. This approach is easy to implement on general‐purpose optical microscopy systems and suitable for use in cell biology in a wide variety of applications. |
topic |
cell‐instructive substrates cell migration cell orientation light‐responsive polymers optical manipulation |
url |
https://doi.org/10.1002/advs.201801826 |
work_keys_str_mv |
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