Whitehead Lachlan W, McArthur Kate, Geoghegan Niall D, Rogers Kelly L
Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Immunol Cell Biol. 2017 Jul;95(6):520-524. doi: 10.1038/icb.2017.36. Epub 2017 Apr 27.
In just over a decade, the field of biomedical research has witnessed a radical evolution in technologies for the 3- and 4-dimensional imaging of biological samples. Light sheet fluorescence microscopy is quickly developing into a powerful approach for fast, volumetric imaging of cells, tissues and living organisms. This review touches on the development of 3-dimensional imaging, from its foundations, namely from the invention of confocal microscopy in the twentieth century to more recent examples, notably the IsoView SPIM, the Lattice Light Sheet Microscope and swept confocally aligned planar excitation. These technologies overcome the limitations of conventional optical sectioning techniques and enable unprecedented levels of spatio-temporal resolution with low levels of phototoxicity. Developing in parallel with powerful computational approaches, light sheet based methods promise to completely transform cell biology as we know it today.
在短短十多年的时间里,生物医学研究领域见证了生物样本三维和四维成像技术的彻底变革。光片荧光显微镜正迅速发展成为一种用于细胞、组织和生物体快速体积成像的强大方法。本文综述了三维成像的发展历程,从其基础,即二十世纪共聚焦显微镜的发明,到更多近期的实例,特别是IsoView SPIM、晶格光片显微镜和扫描共焦排列平面激发技术。这些技术克服了传统光学切片技术的局限性,能够以低光毒性实现前所未有的时空分辨率。与强大的计算方法并行发展,基于光片的方法有望彻底改变我们如今所知的细胞生物学。