Department of Bioengineering, University of Pennsylvania, 220 S 33rd St, Philadelphia, PA 19104, USA.
Ann Biomed Eng. 2012 Jan;40(1):23-36. doi: 10.1007/s10439-011-0390-6. Epub 2011 Oct 13.
Despite its enormous incidence, mild traumatic brain injury is not well understood. One aspect that needs more definition is how the mechanical energy during injury affects neural circuit function. Recent developments in cellular imaging probes provide an opportunity to assess the dynamic state of neural networks with single-cell resolution. In this article, we developed imaging methods to assess the state of dissociated cortical networks exposed to mild injury. We estimated the imaging conditions needed to achieve accurate measures of network properties, and applied these methodologies to evaluate if mild mechanical injury to cortical neurons produces graded changes to either spontaneous network activity or altered network topology. We found that modest injury produced a transient increase in calcium activity that dissipated within 1 h after injury. Alternatively, moderate mechanical injury produced immediate disruption in network synchrony, loss in excitatory tone, and increased modular topology. A calcium-activated neutral protease (calpain) was a key intermediary in these changes; blocking calpain activation restored the network nearly completely to its pre-injury state. Together, these findings show a more complex change in neural circuit behavior than previously reported for mild mechanical injury, and highlight at least one important early mechanism responsible for these changes.
尽管轻度创伤性脑损伤的发病率很高,但人们对此了解甚少。需要进一步明确的一个方面是,损伤过程中的机械能如何影响神经回路功能。细胞成像探针的最新进展为评估具有单细胞分辨率的神经网络的动态状态提供了机会。在本文中,我们开发了成像方法来评估暴露于轻度损伤的分离皮质网络的状态。我们估计了实现网络特性准确测量所需的成像条件,并应用这些方法学来评估皮质神经元的轻度机械损伤是否会导致自发网络活动或改变的网络拓扑结构产生分级变化。我们发现适度的损伤会产生短暂的钙活性增加,这种增加会在损伤后 1 小时内消散。相反,中度机械损伤会立即破坏网络同步,降低兴奋性,并增加模块拓扑结构。钙激活中性蛋白酶(钙蛋白酶)是这些变化的关键中介;阻断钙蛋白酶的激活可使网络几乎完全恢复到损伤前的状态。总之,这些发现表明,与之前报道的轻度机械损伤相比,神经回路行为发生了更为复杂的变化,并强调了至少一种导致这些变化的重要早期机制。