Response to Blast-like Shear Stresses Associated with Mild Blast-Induced Brain Injury

被引:5
|
作者
Ravin, Rea [1 ]
Morgan, Nicole Y. [2 ]
Blank, Paul S. [3 ]
Ravin, Nitay [1 ]
Guerrero-Cazares, Hugo [4 ]
Quinones-Hinojosa, Alfredo [4 ]
Zimmerberg, Joshua [3 ]
机构
[1] Celoptics Inc, Rockville, MD USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Natl Inst Biomed Imaging & Bioengn, NIH, Bethesda, MD USA
[3] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Integrat Biophys, Div Basic & Translat Biophys, NIH, Bethesda, MD 20892 USA
[4] Johns Hopkins Univ, Dept Neurosurg, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
IN-VITRO; MODEL; WAVE;
D O I
10.1016/j.bpj.2019.07.052
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:1167 / 1178
页数:12
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