Alencar Herlen, Mahmood Umar, Kawano Yoshihiro, Hirata Tadashi, Weissleder Ralph
Center for Molecular Imaging Research, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
Neoplasia. 2005 Nov;7(11):977-83. doi: 10.1593/neo.05376.
Real-time in vivo imaging of molecular targets at (sub)cellular resolution is essential in better understanding complex biology. Confocal microscopy and multiphoton microscopy have been used in the past to achieve this goal, but their true capabilities have often been limited by bulky optics and difficult experimental set-ups requiring exteriorized organs. We describe here the development and validation of a unique near-infrared laser scanning microscope system that uses novel optics with a millimeter footprint. Optimized for use in the far red and near-infrared ranges, the system allows an imaging depth that extends up to 500 microm from a 1.3-mm-diameter stick objective, which is up to 2 cm in length. We show exceptionally high spatial, temporal, and multiwavelength resolutions of the system and show that it can be applied to virtually any internal organ through a keyhole surgical access. We demonstrate that, when combined with novel far red imaging probes, it is possible to image the cellular details of many organs and disease processes. The new optics, coupled with the use of near-infrared probes, should prove immensely valuable for in vivo cancer imaging.
以(亚)细胞分辨率对分子靶点进行实时体内成像对于更好地理解复杂生物学至关重要。过去曾使用共聚焦显微镜和多光子显微镜来实现这一目标,但它们的真正能力常常受到笨重光学器件以及需要将器官外置的复杂实验设置的限制。我们在此描述一种独特的近红外激光扫描显微镜系统的开发与验证,该系统采用了占地面积仅为毫米级的新型光学器件。该系统针对远红光和近红外波段进行了优化,使用直径1.3毫米、长度达2厘米的棒状物镜时,成像深度可达500微米。我们展示了该系统极高的空间、时间和多波长分辨率,并表明通过锁孔手术通路,它几乎可以应用于任何内部器官。我们证明,当与新型远红光成像探针结合使用时,能够对许多器官和疾病过程的细胞细节进行成像。这种新型光学器件与近红外探针的结合,对于体内癌症成像应具有巨大价值。