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Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo

机译:成像神经变性的多个阶段:一种评估体内细胞死亡的新方法

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Nerve cell death is the key event in all neurodegenerative disorders, with apoptosis and necrosis being central to both acute and chronic degenerative processes. However, until now, it has not been possible to study these dynamically and in real time. In this study, we use spectrally distinct, well-recognised fluorescent cell death markers to enable the temporal resolution and quantification of the early and late phases of apoptosis and necrosis of single nerve cells in different disease models. The tracking of single-cell death profiles in the same living eye over hours, days, weeks and months is a significant advancement on currently available techniques. We identified a numerical preponderance of late-phase versus early-phase apoptotic cells in chronic models, reinforcing the commonalities between cellular mechanisms in different disease models. We showed that MK801 effectively inhibited both apoptosis and necrosis, but our findings support the use of our technique to investigate more specific anti-apoptotic and anti-necrotic strategies with well-defined targets, with potentially greater clinical application. The optical properties of the eye provide compelling opportunities for the quantitative monitoring of disease mechanisms and dynamics in experimental neurodegeneration. Our findings also help to directly observe retinal nerve cell death in patients as an adjunct to refining diagnosis, tracking disease status and assessing therapeutic intervention.. ? 2010 Macmillan Publishers Limited
机译:神经细胞死亡是所有神经退行性疾病的关键事件,凋亡和坏死是急性和慢性退行性过程的关键。但是,到目前为止,还不可能动态地,实时地研究这些内容。在这项研究中,我们使用光谱上独特的,公认的荧光细胞死亡标记来实现时间分辨和定量分析不同疾病模型中单个神经细胞凋亡和坏死的早期和晚期。在数小时,数天,数周和数月内,同一只活着的眼睛中单细胞死亡概况的追踪是当前可用技术的一项重大进步。我们确定了慢性模型中晚期凋亡细胞与早期凋亡细胞的数量优势,从而增强了不同疾病模型中细胞机制之间的共性。我们表明,MK801有效抑制细胞凋亡和坏死,但我们的发现支持使用我们的技术来研究具有明确目标的更具体的抗凋亡和抗坏死策略,并可能在临床上有更大的应用。眼睛的光学特性为定量监测实验性神经变性中的疾病机制和动力学提供了令人信服的机会。我们的发现还有助于直接观察患者的视网膜神经细胞死亡,作为完善诊断,跟踪疾病状态和评估治疗干预的辅助手段。 2010 Macmillan Publishers Limited

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