胚胎发育动态成像的快速荧光显微镜。

Hfsp Journal Pub Date : 2008-06-01 Epub Date: 2008-05-13 DOI:10.2976/1.2907579
Julien Vermot, Scott E Fraser, Michael Liebling
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引用次数: 74

摘要

实时成像在发育生物学中发挥了关键作用,因为它越来越多地允许对完整生物体中的细胞行为进行实时观察。能够捕捉更快生物事件动态的显微镜,最适合体内成像的荧光标记,最后,适应的重建和分析程序来完成数据流,都有助于这一成功。聚焦于时间分辨率,我们讨论如何快速成像可以实现最小的偏见空间分辨率,光子计数,或可靠和自动分析图像。特别是,我们展示了如何将明亮的荧光探针、快速显微镜和定制后处理技术相结合的综合成像方法可以在多个尺度上解决生物系统的动力学问题。最后,我们讨论了该领域进一步发展的挑战和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast fluorescence microscopy for imaging the dynamics of embryonic development.

Live imaging has gained a pivotal role in developmental biology since it increasingly allows real-time observation of cell behavior in intact organisms. Microscopes that can capture the dynamics of ever-faster biological events, fluorescent markers optimal for in vivo imaging, and, finally, adapted reconstruction and analysis programs to complete data flow all contribute to this success. Focusing on temporal resolution, we discuss how fast imaging can be achieved with minimal prejudice to spatial resolution, photon count, or to reliably and automatically analyze images. In particular, we show how integrated approaches to imaging that combine bright fluorescent probes, fast microscopes, and custom post-processing techniques can address the kinetics of biological systems at multiple scales. Finally, we discuss remaining challenges and opportunities for further advances in this field.

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Hfsp Journal
Hfsp Journal 综合性期刊-综合性期刊
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