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...

Full description

Bibliographic Details
Main Authors: Mohammad M. Maneshi, Frederick Sachs, Susan Z. Hua
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fncel.2018.00069/full
id doaj-0014abe6a9054d268b41b9bbf271761d
record_format Article
spelling 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 AT mohammadmmaneshi heterogeneouscytoskeletalforcedistributiondelineatestheonsetca2influxunderfluidshearstressinastrocytes
AT mohammadmmaneshi heterogeneouscytoskeletalforcedistributiondelineatestheonsetca2influxunderfluidshearstressinastrocytes
AT fredericksachs heterogeneouscytoskeletalforcedistributiondelineatestheonsetca2influxunderfluidshearstressinastrocytes
AT susanzhua heterogeneouscytoskeletalforcedistributiondelineatestheonsetca2influxunderfluidshearstressinastrocytes
AT susanzhua heterogeneouscytoskeletalforcedistributiondelineatestheonsetca2influxunderfluidshearstressinastrocytes
_version_ 1725445227089494016