Literature DB >> 26958893

Intracellular Pressure Dynamics in Blebbing Cells.

Wanda Strychalski1, Robert D Guy2.   

Abstract

Blebs are pressure-driven protrusions that play an important role in cell migration, particularly in three-dimensional environments. A bleb is initiated when the cytoskeleton detaches from the cell membrane, resulting in the pressure-driven flow of cytosol toward the area of detachment and local expansion of the cell membrane. Recent experiments involving blebbing cells have led to conflicting hypotheses regarding the timescale of intracellular pressure propagation. The interpretation of one set of experiments supports a poroelastic model of the cytoplasm that leads to slow pressure equilibration when compared to the timescale of bleb expansion. A different study concludes that pressure equilibrates faster than the timescale of bleb expansion. To address this discrepancy, a dynamic computational model of the cell was developed that includes mechanics of and the interactions among the cytoplasm, the actin cortex, the cell membrane, and the cytoskeleton. The model results quantify the relationship among cytoplasmic rheology, pressure, and bleb expansion dynamics, and provide a more detailed picture of intracellular pressure dynamics. This study shows the elastic response of the cytoplasm relieves pressure and limits bleb size, and that both permeability and elasticity of the cytoplasm determine bleb expansion time. Our model with a poroelastic cytoplasm shows that pressure disturbances from bleb initiation propagate faster than the timescale of bleb expansion and that pressure equilibrates slower than the timescale of bleb expansion. The multiple timescales in intracellular pressure dynamics explain the apparent discrepancy in the interpretation of experimental results.
Copyright © 2016 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Mesh:

Year:  2016        PMID: 26958893      PMCID: PMC4788720          DOI: 10.1016/j.bpj.2016.01.012

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  26 in total

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Authors:  Kunito Yoshida; Thierry Soldati
Journal:  J Cell Sci       Date:  2006-08-22       Impact factor: 5.285

Review 3.  Blebs lead the way: how to migrate without lamellipodia.

Authors:  Guillaume Charras; Ewa Paluch
Journal:  Nat Rev Mol Cell Biol       Date:  2008-07-16       Impact factor: 94.444

Review 4.  A short history of blebbing.

Authors:  G T Charras
Journal:  J Microsc       Date:  2008-09       Impact factor: 1.758

Review 5.  Implications of a poroelastic cytoplasm for the dynamics of animal cell shape.

Authors:  T J Mitchison; G T Charras; L Mahadevan
Journal:  Semin Cell Dev Biol       Date:  2008-02-07       Impact factor: 7.727

6.  Life and times of a cellular bleb.

Authors:  Guillaume T Charras; Margaret Coughlin; Timothy J Mitchison; L Mahadevan
Journal:  Biophys J       Date:  2007-10-05       Impact factor: 4.033

7.  Traction stress analysis and modeling reveal that amoeboid migration in confined spaces is accompanied by expansive forces and requires the structural integrity of the membrane-cortex interactions.

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Journal:  Integr Biol (Camb)       Date:  2015-06-08       Impact factor: 2.192

Review 8.  Cortical flow in animal cells.

Authors:  D Bray; J G White
Journal:  Science       Date:  1988-02-19       Impact factor: 47.728

9.  Animal cell hydraulics.

Authors:  Guillaume T Charras; Timothy J Mitchison; L Mahadevan
Journal:  J Cell Sci       Date:  2009-08-18       Impact factor: 5.285

10.  Reassembly of contractile actin cortex in cell blebs.

Authors:  Guillaume T Charras; Chi-Kuo Hu; Margaret Coughlin; Timothy J Mitchison
Journal:  J Cell Biol       Date:  2006-11-06       Impact factor: 10.539

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  16 in total

1.  Cell Surface Mechanochemistry and the Determinants of Bleb Formation, Healing, and Travel Velocity.

Authors:  Kathryn Manakova; Huaming Yan; John Lowengrub; Jun Allard
Journal:  Biophys J       Date:  2016-04-12       Impact factor: 4.033

2.  An Immersed Boundary method with divergence-free velocity interpolation and force spreading.

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Journal:  J Comput Phys       Date:  2017-06-28       Impact factor: 3.553

3.  A reduced 1D stochastic model of bleb-driven cell migration.

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4.  A role for myosin II clusters and membrane energy in cortex rupture for Dictyostelium discoideum.

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Journal:  PLoS One       Date:  2022-04-25       Impact factor: 3.752

5.  Going with the Flow: Water Flux and Cell Shape during Cytokinesis.

Authors:  Yizeng Li; Lijuan He; Nicolas A P Gonzalez; Jenna Graham; Charles Wolgemuth; Denis Wirtz; Sean X Sun
Journal:  Biophys J       Date:  2017-12-05       Impact factor: 4.033

6.  Potential Hydrodynamic Cytoplasmic Transfer between Mammalian Cells: Cell-Projection Pumping.

Authors:  Hans Zoellner; Navid Paknejad; James A Cornwell; Belal Chami; Yevgeniy Romin; Vitaly Boyko; Sho Fujisawa; Elizabeth Kelly; Garry W Lynch; Glynn Rogers; Katia Manova; Malcolm A S Moore
Journal:  Biophys J       Date:  2020-01-31       Impact factor: 4.033

7.  Differences in creep response of GBM cells migrating in confinement.

Authors:  Ishan Khan; Loan Bui; Robert Bachoo; Young-Tae Kim; Cheng-Jen Chuong
Journal:  Int Biomech       Date:  2020-12

8.  Cell nucleus as a microrheological probe to study the rheology of the cytoskeleton.

Authors:  Moslem Moradi; Ehssan Nazockdast
Journal:  Biophys J       Date:  2021-03-09       Impact factor: 4.033

9.  A free-boundary model of a motile cell explains turning behavior.

Authors:  Masoud Nickaeen; Igor L Novak; Stephanie Pulford; Aaron Rumack; Jamie Brandon; Boris M Slepchenko; Alex Mogilner
Journal:  PLoS Comput Biol       Date:  2017-11-14       Impact factor: 4.475

10.  BioFlow: a non-invasive, image-based method to measure speed, pressure and forces inside living cells.

Authors:  Aleix Boquet-Pujadas; Timothée Lecomte; Maria Manich; Roman Thibeaux; Elisabeth Labruyère; Nancy Guillén; Jean-Christophe Olivo-Marin; Alexandre C Dufour
Journal:  Sci Rep       Date:  2017-08-23       Impact factor: 4.379

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