Real-time dynamics of emerging actin networks in cell-mimicking compartments
Understanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in cell motility, environmental exploration, intracellular transport and mechanical stability. Though the viscoelastic properties of actin-based structures have been extensively probed, the underlying microstructure dynamics, especially their disassembly, is not fully understood. In this article, we explore the rich dynamics and emergent properties exhibited by actin bundles within flow-free confinements using a microfluidic set-up and epifluorescence microscopy. After forming entangled actin filaments within cell-sized quasi two-dimensional confinements, we induce their bundling using three different fundamental mechanisms: counterion condensation, depletion interactions and specific protein-protein interactions. Intriguingly, long actin filaments form emerging networks of actin bundles via percolation leading to remarkable properties such as stress generation and spindle-like intermediate structures. Simultaneous sharing of filaments in different links of the network is an important parameter, as short filaments do not form networks but segregated clusters of bundles instead. We encounter a hierarchical process of bundling and its subsequent disassembly. Additionally, our study suggests that such percolated networks are likely to exist within living cells in a dynamic fashion. These observations render a perspective about differential cytoskeletal responses towards numerous stimuli.
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dig-wur-nl-wurpubs-6047022024-12-04 Deshpande, Siddharth Pfohl, Thomas Article/Letter to editor PLoS ONE 10 (2015) 3 ISSN: 1932-6203 Real-time dynamics of emerging actin networks in cell-mimicking compartments 2015 Understanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in cell motility, environmental exploration, intracellular transport and mechanical stability. Though the viscoelastic properties of actin-based structures have been extensively probed, the underlying microstructure dynamics, especially their disassembly, is not fully understood. In this article, we explore the rich dynamics and emergent properties exhibited by actin bundles within flow-free confinements using a microfluidic set-up and epifluorescence microscopy. After forming entangled actin filaments within cell-sized quasi two-dimensional confinements, we induce their bundling using three different fundamental mechanisms: counterion condensation, depletion interactions and specific protein-protein interactions. Intriguingly, long actin filaments form emerging networks of actin bundles via percolation leading to remarkable properties such as stress generation and spindle-like intermediate structures. Simultaneous sharing of filaments in different links of the network is an important parameter, as short filaments do not form networks but segregated clusters of bundles instead. We encounter a hierarchical process of bundling and its subsequent disassembly. Additionally, our study suggests that such percolated networks are likely to exist within living cells in a dynamic fashion. These observations render a perspective about differential cytoskeletal responses towards numerous stimuli. en text/html https://research.wur.nl/en/publications/real-time-dynamics-of-emerging-actin-networks-in-cell-mimicking-c 10.1371/journal.pone.0116521 https://edepot.wur.nl/581257 Life Science https://creativecommons.org/licenses/by/4.0/ Wageningen University & Research |
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Life Science Life Science Deshpande, Siddharth Pfohl, Thomas Real-time dynamics of emerging actin networks in cell-mimicking compartments |
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Understanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in cell motility, environmental exploration, intracellular transport and mechanical stability. Though the viscoelastic properties of actin-based structures have been extensively probed, the underlying microstructure dynamics, especially their disassembly, is not fully understood. In this article, we explore the rich dynamics and emergent properties exhibited by actin bundles within flow-free confinements using a microfluidic set-up and epifluorescence microscopy. After forming entangled actin filaments within cell-sized quasi two-dimensional confinements, we induce their bundling using three different fundamental mechanisms: counterion condensation, depletion interactions and specific protein-protein interactions. Intriguingly, long actin filaments form emerging networks of actin bundles via percolation leading to remarkable properties such as stress generation and spindle-like intermediate structures. Simultaneous sharing of filaments in different links of the network is an important parameter, as short filaments do not form networks but segregated clusters of bundles instead. We encounter a hierarchical process of bundling and its subsequent disassembly. Additionally, our study suggests that such percolated networks are likely to exist within living cells in a dynamic fashion. These observations render a perspective about differential cytoskeletal responses towards numerous stimuli. |
format |
Article/Letter to editor |
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Life Science |
author |
Deshpande, Siddharth Pfohl, Thomas |
author_facet |
Deshpande, Siddharth Pfohl, Thomas |
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Deshpande, Siddharth |
title |
Real-time dynamics of emerging actin networks in cell-mimicking compartments |
title_short |
Real-time dynamics of emerging actin networks in cell-mimicking compartments |
title_full |
Real-time dynamics of emerging actin networks in cell-mimicking compartments |
title_fullStr |
Real-time dynamics of emerging actin networks in cell-mimicking compartments |
title_full_unstemmed |
Real-time dynamics of emerging actin networks in cell-mimicking compartments |
title_sort |
real-time dynamics of emerging actin networks in cell-mimicking compartments |
url |
https://research.wur.nl/en/publications/real-time-dynamics-of-emerging-actin-networks-in-cell-mimicking-c |
work_keys_str_mv |
AT deshpandesiddharth realtimedynamicsofemergingactinnetworksincellmimickingcompartments AT pfohlthomas realtimedynamicsofemergingactinnetworksincellmimickingcompartments |
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1819148062671503360 |