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Spectral Fingerprinting of Individual Cells Visualized by Cavity-Reflection-Enhanced Light-Absorption Microscopy

机译:腔反射增强光吸收显微镜可视化的单个细胞的光谱指纹图谱。

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摘要

The absorption spectrum of light is known to be a “molecular fingerprint” that enables analysis of the molecular type and its amount. It would be useful to measure the absorption spectrum in single cell in order to investigate the cellular status. However, cells are too thin for their absorption spectrum to be measured. In this study, we developed an optical-cavity-enhanced absorption spectroscopic microscopy method for two-dimensional absorption imaging. The light absorption is enhanced by an optical cavity system, which allows the detection of the absorption spectrum with samples having an optical path length as small as 10 μm, at a subcellular spatial resolution. Principal component analysis of various types of cultured mammalian cells indicates absorption-based cellular diversity. Interestingly, this diversity is observed among not only different species but also identical cell types. Furthermore, this microscopy technique allows us to observe frozen sections of tissue samples without any staining and is capable of label-free biopsy. Thus, our microscopy method opens the door for imaging the absorption spectra of biological samples and thereby detecting the individuality of cells.
机译:众所周知,光的吸收光谱是“分子指纹”,可以分析分子类型及其数量。测量单细胞的吸收光谱以研究细胞状态将是有用的。但是,细胞太薄,无法测量其吸收光谱。在这项研究中,我们开发了一种用于二维吸收成像的光腔增强吸收光谱显微镜方法。通过光学腔系统增强了光吸收,该系统允许以亚细胞空间分辨率用光程长度小至10μm的样品检测吸收光谱。各种类型的哺乳动物细胞的主成分分析表明,基于吸收的细胞多样性。有趣的是,不仅在不同物种之间,而且在相同细胞类型之间都观察到了这种多样性。此外,这种显微镜技术使我们能够观察组织样品的冷冻切片而无任何染色,并且能够进行无标记的活检。因此,我们的显微镜方法为成像生物样品的吸收光谱从而检测细胞的个性打开了大门。

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