Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes
Mechanical perturbations increase intracellular Ca2+ in cells, but the coupling of mechanical forces to the Ca2+ influx is not well understood. We used a microfluidic chamber driven with a high-speed pressure servo to generate defined fluid shear stress to cultured astrocytes, and simultaneously mea...
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doaj-0014abe6a9054d268b41b9bbf271761d2020-11-25T00:00:25ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022018-03-011210.3389/fncel.2018.00069344424Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in AstrocytesMohammad M. Maneshi0Mohammad M. Maneshi1Frederick Sachs2Susan Z. Hua3Susan Z. Hua4Department of Physiology and Biophysics, University at Buffalo, Buffalo, NY, United StatesDepartment of Mechanical and Aerospace Engineering, University at Buffalo, Buffalo, NY, United StatesDepartment of Physiology and Biophysics, University at Buffalo, Buffalo, NY, United StatesDepartment of Physiology and Biophysics, University at Buffalo, Buffalo, NY, United StatesDepartment of Mechanical and Aerospace Engineering, University at Buffalo, Buffalo, NY, United StatesMechanical perturbations increase intracellular Ca2+ in cells, but the coupling of mechanical forces to the Ca2+ influx is not well understood. We used a microfluidic chamber driven with a high-speed pressure servo to generate defined fluid shear stress to cultured astrocytes, and simultaneously measured cytoskeletal forces using a force sensitive actinin optical sensor and intracellular Ca2+. Fluid shear generated non-uniform forces in actinin that critically depended on the stimulus rise time emphasizing the presence of viscoelasticity in the activating sequence. A short (ms) shear pulse with fast rise time (2 ms) produced an immediate increase in actinin tension at the upstream end of the cell with minimal changes at the downstream end. The onset of Ca2+ rise began at highly strained areas. In contrast to stimulus steps, slow ramp stimuli produced uniform forces throughout the cells and only a small Ca2+ response. The heterogeneity of force distribution is exaggerated in cells having fewer stress fibers and lower pre-tension in actinin. Disruption of cytoskeleton with cytochalasin-D (Cyt-D) eliminated force gradients, and in those cells Ca2+ elevation started from the soma. Thus, Ca2+ influx with a mechanical stimulus depends on local stress within the cell and that is time dependent due to viscoelastic mechanics.http://journal.frontiersin.org/article/10.3389/fncel.2018.00069/fullastrocytescytoskeletal forcestraumatic brain injury (TBI)fluid shear stressFRETmechanosensitive ion channel (MSC) |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammad M. Maneshi Mohammad M. Maneshi Frederick Sachs Susan Z. Hua Susan Z. Hua |
spellingShingle |
Mohammad M. Maneshi Mohammad M. Maneshi Frederick Sachs Susan Z. Hua Susan Z. Hua Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes Frontiers in Cellular Neuroscience astrocytes cytoskeletal forces traumatic brain injury (TBI) fluid shear stress FRET mechanosensitive ion channel (MSC) |
author_facet |
Mohammad M. Maneshi Mohammad M. Maneshi Frederick Sachs Susan Z. Hua Susan Z. Hua |
author_sort |
Mohammad M. Maneshi |
title |
Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes |
title_short |
Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes |
title_full |
Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes |
title_fullStr |
Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes |
title_full_unstemmed |
Heterogeneous Cytoskeletal Force Distribution Delineates the Onset Ca2+ Influx Under Fluid Shear Stress in Astrocytes |
title_sort |
heterogeneous cytoskeletal force distribution delineates the onset ca2+ influx under fluid shear stress in astrocytes |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2018-03-01 |
description |
Mechanical perturbations increase intracellular Ca2+ in cells, but the coupling of mechanical forces to the Ca2+ influx is not well understood. We used a microfluidic chamber driven with a high-speed pressure servo to generate defined fluid shear stress to cultured astrocytes, and simultaneously measured cytoskeletal forces using a force sensitive actinin optical sensor and intracellular Ca2+. Fluid shear generated non-uniform forces in actinin that critically depended on the stimulus rise time emphasizing the presence of viscoelasticity in the activating sequence. A short (ms) shear pulse with fast rise time (2 ms) produced an immediate increase in actinin tension at the upstream end of the cell with minimal changes at the downstream end. The onset of Ca2+ rise began at highly strained areas. In contrast to stimulus steps, slow ramp stimuli produced uniform forces throughout the cells and only a small Ca2+ response. The heterogeneity of force distribution is exaggerated in cells having fewer stress fibers and lower pre-tension in actinin. Disruption of cytoskeleton with cytochalasin-D (Cyt-D) eliminated force gradients, and in those cells Ca2+ elevation started from the soma. Thus, Ca2+ influx with a mechanical stimulus depends on local stress within the cell and that is time dependent due to viscoelastic mechanics. |
topic |
astrocytes cytoskeletal forces traumatic brain injury (TBI) fluid shear stress FRET mechanosensitive ion channel (MSC) |
url |
http://journal.frontiersin.org/article/10.3389/fncel.2018.00069/full |
work_keys_str_mv |
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