Evans Conor L, Potma Eric O, Puoris'haag Mehron, Côté Daniel, Lin Charles P, Xie X Sunney
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 2005 Nov 15;102(46):16807-12. doi: 10.1073/pnas.0508282102. Epub 2005 Nov 1.
Imaging living organisms with molecular selectivity typically requires the introduction of specific labels. Many applications in biology and medicine, however, would significantly benefit from a noninvasive imaging technique that circumvents such exogenous probes. In vivo microscopy based on vibrational spectroscopic contrast offers a unique approach for visualizing tissue architecture with molecular specificity. We have developed a sensitive technique for vibrational imaging of tissues by combining coherent anti-Stokes Raman scattering (CARS) with video-rate microscopy. Backscattering of the intense forward-propagating CARS radiation in tissue gives rise to a strong epi-CARS signal that makes in vivo imaging possible. This substantially large signal allows for real-time monitoring of dynamic processes, such as the diffusion of chemical compounds, in tissues. By tuning into the CH(2) stretching vibrational band, we demonstrate CARS imaging and spectroscopy of lipid-rich tissue structures in the skin of a live mouse, including sebaceous glands, corneocytes, and adipocytes, with unprecedented contrast at subcellular resolution.
对活生物体进行具有分子选择性的成像通常需要引入特定的标记。然而,生物学和医学中的许多应用将从一种无需外源性探针的非侵入性成像技术中显著受益。基于振动光谱对比度的体内显微镜检查为以分子特异性可视化组织结构提供了一种独特的方法。我们通过将相干反斯托克斯拉曼散射(CARS)与视频速率显微镜相结合,开发了一种用于组织振动成像的灵敏技术。组织中强烈向前传播的CARS辐射的背向散射产生了强烈的落射CARS信号,这使得体内成像成为可能。这种相当大的信号允许对组织中的动态过程,如化合物的扩散,进行实时监测。通过调谐到CH(2)伸缩振动带,我们展示了对活小鼠皮肤中富含脂质的组织结构进行CARS成像和光谱分析,包括皮脂腺、角质形成细胞和脂肪细胞,在亚细胞分辨率下具有前所未有的对比度。