Institute for Biological and Medical Imaging, Helmholtz Zentrum München und Technische Universität München, Munich, Germany.
Nat Methods. 2010 Aug;7(8):603-14. doi: 10.1038/nmeth.1483. Epub 2010 Jul 30.
Optical microscopy has been a fundamental tool of biological discovery for more than three centuries, but its in vivo tissue imaging ability has been restricted by light scattering to superficial investigations, even when confocal or multiphoton methods are used. Recent advances in optical and optoacoustic (photoacoustic) imaging now allow imaging at depths and resolutions unprecedented for optical methods. These abilities are increasingly important to understand the dynamic interactions of cellular processes at different systems levels, a major challenge of postgenome biology. This Review discusses promising photonic methods that have the ability to visualize cellular and subcellular components in tissues across different penetration scales. The methods are classified into microscopic, mesoscopic and macroscopic approaches, according to the tissue depth at which they operate. Key characteristics associated with different imaging implementations are described and the potential of these technologies in biological applications is discussed.
光学显微镜已经成为三个多世纪以来生物学发现的基本工具,但由于光散射的限制,即使使用共聚焦或多光子方法,其在体内组织成像的能力也仅限于浅层研究。最近在光学和光声(超声)成像方面的进展现在允许以空前的光学方法的深度和分辨率进行成像。这些能力对于了解不同系统水平的细胞过程的动态相互作用越来越重要,这是后基因组生物学的主要挑战。本文综述了有前途的光子学方法,这些方法有能力在不同穿透尺度的组织中可视化细胞和亚细胞成分。这些方法根据其工作的组织深度分为微观、介观和宏观方法。描述了与不同成像实现相关的关键特征,并讨论了这些技术在生物学应用中的潜力。