TY - JOUR
T1 - Response to Blast-like Shear Stresses Associated with Mild Blast-Induced Brain Injury
AU - Ravin, Rea
AU - Morgan, Nicole Y.
AU - Blank, Paul S.
AU - Ravin, Nitay
AU - Guerrero-Cazares, Hugo
AU - Quinones-Hinojosa, Alfredo
AU - Zimmerberg, Joshua
N1 - Funding Information:
This work was supported by the Intramural Programs of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health , Bethesda, Maryland, and of the National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health , Bethesda, Maryland, as well as the National Institutes of Health Extramural Program under award number R01NS070024 (A.Q.H.); this material is also based upon work supported by the Defense Advanced Research Project Agency and Space and Naval Warfare Systems Center (SPAWARSYSCEN Pacific) under contract no. N66001-14-C-4056 (Celoptics).
Funding Information:
This work was supported by the Intramural Programs of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, and of the National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland, as well as the National Institutes of Health Extramural Program under award number R01NS070024 (A.Q.H.); this material is also based upon work supported by the Defense Advanced Research Project Agency and Space and Naval Warfare Systems Center (SPAWARSYSCEN Pacific) under contract no. N66001-14-C-4056 (Celoptics).
Publisher Copyright:
© 2019
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Toward the goal of understanding the pathophysiology of mild blast-induced traumatic brain injury and identifying the physical forces associated with the primary injury phase, we developed a system that couples a pneumatic blast to a microfluidic channel to precisely and reproducibly deliver shear transients to dissociated human central nervous system (CNS) cells, on a timescale comparable to an explosive blast but with minimal pressure transients. Using fluorescent beads, we have characterized the shear transients experienced by the cells and demonstrate that the system is capable of accurately and reproducibly delivering uniform shear transients with minimal pressure across the cell culture volume. This system is compatible with high-resolution, time-lapse optical microscopy. Using this system, we demonstrate that blast-like shear transients produced with minimal pressure transients and submillisecond rise times activate calcium responses in dissociated human CNS cultures. Cells respond with increased cytosolic free calcium to a threshold shear stress between 8 and 21 Pa; the propagation of this calcium response is a result of purinergic signaling. We propose that this system models, in vitro, the fundamental injury wave produced by shear forces consequent to blast shock waves passing through density inhomogeneity in human CNS cells.
AB - Toward the goal of understanding the pathophysiology of mild blast-induced traumatic brain injury and identifying the physical forces associated with the primary injury phase, we developed a system that couples a pneumatic blast to a microfluidic channel to precisely and reproducibly deliver shear transients to dissociated human central nervous system (CNS) cells, on a timescale comparable to an explosive blast but with minimal pressure transients. Using fluorescent beads, we have characterized the shear transients experienced by the cells and demonstrate that the system is capable of accurately and reproducibly delivering uniform shear transients with minimal pressure across the cell culture volume. This system is compatible with high-resolution, time-lapse optical microscopy. Using this system, we demonstrate that blast-like shear transients produced with minimal pressure transients and submillisecond rise times activate calcium responses in dissociated human CNS cultures. Cells respond with increased cytosolic free calcium to a threshold shear stress between 8 and 21 Pa; the propagation of this calcium response is a result of purinergic signaling. We propose that this system models, in vitro, the fundamental injury wave produced by shear forces consequent to blast shock waves passing through density inhomogeneity in human CNS cells.
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U2 - 10.1016/j.bpj.2019.07.052
DO - 10.1016/j.bpj.2019.07.052
M3 - Article
C2 - 31495447
AN - SCOPUS:85071697609
SN - 0006-3495
VL - 117
SP - 1167
EP - 1178
JO - Biophysical Journal
JF - Biophysical Journal
IS - 7
ER -