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通过一种新型实时成像技术对轴突运输进行分析,揭示了不同的刺猬蛋白转运动力学。

Analysis of axonal trafficking via a novel live-imaging technique reveals distinct hedgehog transport kinetics.

作者信息

Daniele Joseph R, Baqri Rehan M, Kunes Sam

机构信息

Department of Molecular & Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA

Department of Molecular & Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.

出版信息

Biol Open. 2017 May 15;6(5):714-721. doi: 10.1242/bio.024075.

Abstract

The () eye is an ideal model to study development, intracellular signaling, behavior, and neurodegenerative disease. Interestingly, dynamic data are not commonly employed to investigate eye-specific disease models. Using axonal transport of the morphogen Hedgehog (Hh), which is integral to eye-brain development and implicated in stem cell maintenance and neoplastic disease, we demonstrate the ability to comprehensively quantify and characterize its trafficking in various neuron types and a neurodegeneration model in live early third-instar larval We find that neuronal Hh, whose kinetics have not been reported previously, favors fast anterograde transport and varies in speed and flux with respect to axonal position. This suggests distinct trafficking pathways along the axon. Lastly, we report abnormal transport of Hh in an accepted model of photoreceptor neurodegeneration. As a technical complement to existing eye-specific disease models, we demonstrate the ability to directly visualize transport in real time in intact and live animals and track secreted cargoes from the axon to their release points. Particle dynamics can now be precisely calculated and we posit that this method could be conveniently applied to characterizing disease pathogenesis and genetic screening in other established models of neurodegeneration.

摘要

(果蝇)眼睛是研究发育、细胞内信号传导、行为和神经退行性疾病的理想模型。有趣的是,动态数据通常未被用于研究眼部特异性疾病模型。利用形态发生素刺猬蛋白(Hh)的轴突运输,其对眼脑发育至关重要且与干细胞维持和肿瘤疾病有关,我们展示了在活的早期三龄幼虫中全面量化和表征其在各种神经元类型及神经退行性模型中的运输的能力。我们发现,此前尚未报道其动力学的神经元Hh倾向于快速顺向运输,并且在速度和通量方面随轴突位置而变化。这表明沿轴突存在不同的运输途径。最后,我们报道了在一个公认的光感受器神经退行性模型中Hh的异常运输。作为对现有眼部特异性疾病模型的技术补充,我们展示了在完整的活体动物中实时直接可视化运输并追踪从轴突到其释放点的分泌货物的能力。现在可以精确计算粒子动力学,并且我们认为这种方法可以方便地应用于表征其他已建立的神经退行性模型中的疾病发病机制和基因筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab58/5450320/669f7272cf84/biolopen-6-024075-g1.jpg

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