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Mendonca, Tania; Lis-Slimak, Katarzyna; Matheson, Andrew B; Smith, Matthew G; Anane-Adjei, Akosua B; Ashworth, Jennifer C; Cavanagh, Robert; Paterson, Lynn; Dalgarno, Paul A; Alexander, Cameron; Tassieri, Manlio; Merry, Catherine L R; Wright, Amanda J
OptoRheo: Simultaneous in situ micro-mechanical sensing and imaging of live 3D biological systems Journal Article
In: Commun. Biol., vol. 6, no. 1, pp. 463, 2023.
Abstract | Tags: 3D in vitro models, Biomaterials (hydrogels scaffolds), cell matrix interactions, light sheet fluorescence microscopy, microrheology, multiplane microscopy, optical trapping, Optical tweezers, viscoelasticity
@article{Mendonca2023-hi,
title = {OptoRheo: Simultaneous in situ micro-mechanical sensing and imaging of live 3D biological systems},
author = {Tania Mendonca and Katarzyna Lis-Slimak and Andrew B Matheson and Matthew G Smith and Akosua B Anane-Adjei and Jennifer C Ashworth and Robert Cavanagh and Lynn Paterson and Paul A Dalgarno and Cameron Alexander and Manlio Tassieri and Catherine L R Merry and Amanda J Wright},
year = {2023},
date = {2023-04-01},
urldate = {2023-04-01},
journal = {Commun. Biol.},
volume = {6},
number = {1},
pages = {463},
abstract = {Biomechanical cues from the extracellular matrix (ECM) are
essential for directing many cellular processes, from normal
development and repair, to disease progression. To better
understand cell-matrix interactions, we have developed a new
instrument named \'OptoRheo\' that combines light sheet
fluorescence microscopy with particle tracking microrheology.
OptoRheo lets us image cells in 3D as they proliferate over
several days while simultaneously sensing the mechanical
properties of the surrounding extracellular and pericellular
matrix at a sub-cellular length scale. OptoRheo can be used in
two operational modalities (with and without an optical trap) to
extend the dynamic range of microrheology measurements. We
corroborated this by characterising the ECM surrounding live
breast cancer cells in two distinct culture systems, cell
clusters in 3D hydrogels and spheroids in suspension culture.
This cutting-edge instrument will transform the exploration of
drug transport through complex cell culture matrices and optimise
the design of the next-generation of disease models.},
keywords = {3D in vitro models, Biomaterials (hydrogels scaffolds), cell matrix interactions, light sheet fluorescence microscopy, microrheology, multiplane microscopy, optical trapping, Optical tweezers, viscoelasticity},
pubstate = {published},
tppubtype = {article}
}
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