Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Nat Protoc. 2013 Apr;8(4):810-9. doi: 10.1038/nprot.2013.042.
Live-imaging technology has markedly advanced in the field of neural injury and axon degeneration; however, studies are still predominantly performed in in vitro settings such as cultured neuronal cells or in model organisms such as Caenorhabditis elegans in which axons lack glial wrappings. We recently developed a new in vivo model for adult-stage neural injury in Drosophila melanogaster, using the highly accessible wing of the animal. Because the Drosophila wing is translucent and dispensable for survival, it allows clear and direct visualization of injury-induced progressive responses of axons and glia highlighted by fluorescent protein (FP) markers in live animals over time. Moreover, unlike previous Drosophila models of neural injury, this procedure does not require dissection of the CNS. Thus, the key preparation steps for in vivo imaging of the neural injury response described in this protocol can be completed within 30 min.
在神经损伤和轴突退化领域,活体成像技术取得了显著进展;然而,研究仍然主要在体外环境中进行,如培养的神经元细胞或秀丽隐杆线虫等模式生物,这些模型中的轴突缺乏神经胶质包裹。我们最近在果蝇中开发了一种新的成年期神经损伤的活体模型,利用了动物的高度可及的翅膀。由于果蝇的翅膀是半透明的,对生存不是必需的,因此它可以在活体动物中随时间清晰和直接地观察到荧光蛋白(FP)标记的轴突和神经胶质的损伤诱导的渐进反应。此外,与之前的果蝇神经损伤模型不同,该程序不需要对 CNS 进行解剖。因此,本方案中描述的神经损伤反应活体成像的关键准备步骤可以在 30 分钟内完成。