Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation
Abstract The transfer of mechanical signals through cells is a complex phenomenon. To uncover a new mechanotransduction pathway, we study the frequency-dependent transport of mechanical stimuli by single microtubules and small networks in a bottom-up approach using optically trapped beads as anchor...
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2017-06-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-017-04415-z |
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doaj-6ff609a09ce4425dbf1fc912d19d258a2020-12-08T00:34:51ZengNature Publishing GroupScientific Reports2045-23222017-06-017111510.1038/s41598-017-04415-zSingle microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulationMatthias D. Koch0Natalie Schneider1Peter Nick2Alexander Rohrbach3Laboratory for Bio- and Nano-Photonics, Department of Microsystems Engineering, University of FreiburgMolecular Cell Biology, Botanical Institute, Karlsruhe Institute of TechnologyMolecular Cell Biology, Botanical Institute, Karlsruhe Institute of TechnologyLaboratory for Bio- and Nano-Photonics, Department of Microsystems Engineering, University of FreiburgAbstract The transfer of mechanical signals through cells is a complex phenomenon. To uncover a new mechanotransduction pathway, we study the frequency-dependent transport of mechanical stimuli by single microtubules and small networks in a bottom-up approach using optically trapped beads as anchor points. We interconnected microtubules to linear and triangular geometries to perform micro-rheology by defined oscillations of the beads relative to each other. We found a substantial stiffening of single filaments above a characteristic transition frequency of 1–30 Hz depending on the filament’s molecular composition. Below this frequency, filament elasticity only depends on its contour and persistence length. Interestingly, this elastic behavior is transferable to small networks, where we found the surprising effect that linear two filament connections act as transistor-like, angle dependent momentum filters, whereas triangular networks act as stabilizing elements. These observations implicate that cells can tune mechanical signals by temporal and spatial filtering stronger and more flexibly than expected.https://doi.org/10.1038/s41598-017-04415-z |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Matthias D. Koch Natalie Schneider Peter Nick Alexander Rohrbach |
spellingShingle |
Matthias D. Koch Natalie Schneider Peter Nick Alexander Rohrbach Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation Scientific Reports |
author_facet |
Matthias D. Koch Natalie Schneider Peter Nick Alexander Rohrbach |
author_sort |
Matthias D. Koch |
title |
Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
title_short |
Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
title_full |
Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
title_fullStr |
Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
title_full_unstemmed |
Single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
title_sort |
single microtubules and small networks become significantly stiffer on short time-scales upon mechanical stimulation |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-06-01 |
description |
Abstract The transfer of mechanical signals through cells is a complex phenomenon. To uncover a new mechanotransduction pathway, we study the frequency-dependent transport of mechanical stimuli by single microtubules and small networks in a bottom-up approach using optically trapped beads as anchor points. We interconnected microtubules to linear and triangular geometries to perform micro-rheology by defined oscillations of the beads relative to each other. We found a substantial stiffening of single filaments above a characteristic transition frequency of 1–30 Hz depending on the filament’s molecular composition. Below this frequency, filament elasticity only depends on its contour and persistence length. Interestingly, this elastic behavior is transferable to small networks, where we found the surprising effect that linear two filament connections act as transistor-like, angle dependent momentum filters, whereas triangular networks act as stabilizing elements. These observations implicate that cells can tune mechanical signals by temporal and spatial filtering stronger and more flexibly than expected. |
url |
https://doi.org/10.1038/s41598-017-04415-z |
work_keys_str_mv |
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