Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Cell and Developmental Biology Graduate Program, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Ann Biomed Eng. 2024 Apr;52(4):1021-1038. doi: 10.1007/s10439-023-03438-0. Epub 2024 Jan 31.
Traumatic brain injury (TBI) is the leading cause of accident-related death and disability in the world and can lead to long-term neuropsychiatric symptoms, such as a decline in cognitive function and neurodegeneration. TBI includes primary and secondary injury, with head trauma and deformation of the brain caused by the physical force of the impact as primary injury, and cellular and molecular cascades that lead to cell death as secondary injury. Currently, there is no treatment for TBI-induced cell damage and neural circuit dysfunction in the brain, and thus, it is important to understand the underlying cellular mechanisms that lead to cell damage. In the current study, we use stretchable microelectrode arrays (sMEAs) to model the primary injury of TBI to study the electrophysiological effects of physically injuring cortical cells. We recorded electrophysiological activity before injury and then stretched the flexible membrane of the sMEAs to injure the cells to varying degrees. At 1, 24, and 72 h post-stretch, we recorded activity to analyze differences in spike rate, Fano factor, burstlet rate, burstlet width, synchrony of firing, local network efficiency, and Q statistic. Our results demonstrate that mechanical injury changes the firing properties of cortical neuron networks in culture in a time- and severity-dependent manner. Our results suggest that changes to electrophysiological properties after stretch are dependent on the strength of synchronization between neurons prior to injury.
创伤性脑损伤 (TBI) 是世界上导致事故相关死亡和残疾的主要原因,可导致长期神经精神症状,如认知功能下降和神经退行性变。TBI 包括原发性和继发性损伤,头部创伤和脑变形引起的物理力冲击是原发性损伤,而导致细胞死亡的细胞和分子级联反应是继发性损伤。目前,对于 TBI 引起的脑内细胞损伤和神经回路功能障碍尚无治疗方法,因此,了解导致细胞损伤的潜在细胞机制非常重要。在本研究中,我们使用可拉伸微电极阵列 (sMEA) 来模拟 TBI 的原发性损伤,以研究物理损伤皮质细胞的电生理效应。我们在损伤前记录电生理活动,然后拉伸 sMEA 的柔性膜,以不同程度地损伤细胞。在拉伸后 1、24 和 72 小时,我们记录活动以分析尖峰率、Fano 因子、爆发率、爆发宽度、点火同步性、局部网络效率和 Q 统计的差异。我们的结果表明,机械损伤以时间和严重程度依赖的方式改变培养中皮质神经元网络的点火特性。我们的结果表明,拉伸后电生理特性的变化取决于损伤前神经元之间同步性的强度。