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Cold Shock Induces Apoptosis of Dorsal Root Ganglion Neurons Plated on Infrared Windows

机译:冷休克诱导镀在红外窗户上的背根神经节神经元凋亡

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摘要

The chemical status of live sensory neurons is accessible with infrared microspectroscopy of appropriately prepared cells. In this paper, individual dorsal root ganglion (DRG) neurons have been prepared with two different protocols, and plated on glass cover slips, BaF2 and CaF2 substrates. The first protocol exposes the intact DRGs to 4°C for between 20-30 minutes before dissociating individual neurons and plating 2 hours later. The second protocol maintains the neurons at 23°C for the entire duration of the sample preparation. The visual appearance of the neurons is similar. The viability was assessed by means of trypan blue exclusion method to determine the viability of the neurons. The neurons prepared under the first protocol (cold exposure) and plated on BaF2 reveal a distinct chemical signature and chemical distribution that is different from the other sample preparations described in the paper. Importantly, results for other sample preparation methods, using various substrates and temperature protocols, when compared across the overlapping spectral bandwidth, present normal chemical distribution within the neurons. The unusual chemically specific spatial variation is dominated by a lack of protein and carbohydrates in the center of the neurons and signatures of unraveling DNA are detected. We suggest that cold shock leads to apoptosis of DRGs, followed by osmotic stress originating from ion gradients across the cell membrane leading to cell lysis.
机译:可以通过适当准备的细胞的红外显微技术获得活体感觉神经元的化学状态。在本文中,已经用两种不同的方法制备了单个背根神经节(DRG)神经元,并将其镀在玻璃盖玻片BaF2和CaF2基底上。第一个协议将完整的DRG暴露在4°C下20-30分钟,然后解离单个神经元并在2小时后进行铺板。第二种方案在整个样品制备过程中将神经元维持在23°C。神经元的视觉外观相似。通过锥虫蓝排除法评估生存力,以确定神经元的生存力。按照第一种方法(冷暴露)制备并涂在BaF2上的神经元显示出与本文所述的其他样品制备方法不同的独特化学特征和化学分布。重要的是,使用重叠的光谱带宽进行比较时,使用各种底物和温度协议的其他样品制备方法的结果呈现出神经元内的正常化学分布。这种异常的化学特异的空间变异主要是由于神经元中心缺乏蛋白质和碳水化合物,并且检测到了解开DNA的特征。我们建议冷休克导致DRGs凋亡,随后渗透应力源自细胞膜上的离子梯度导致细胞溶解。

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