Terbium ion as RNA tag for slide-free pathology with deep-ultraviolet excitation fluorescence

被引:7
|
作者
Kumamoto, Yasuaki [1 ]
Matsumoto, Tatsuya [1 ,2 ]
Tanaka, Hideo [1 ]
Takamatsu, Tetsuro [3 ]
机构
[1] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Pathol & Cell Regulat, Kamigyo Ku, 465 Kajiicho, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Div Digest Surg, Kamigyo Ku, 465 Kajiicho, Kyoto 6028566, Japan
[3] Kyoto Prefectural Univ Med, Dept Med Photon, Kamigyo Ku, 465 Kajiicho, Kyoto 6028566, Japan
关键词
ENERGY-TRANSFER; PROBES; COMPLEXES; LUMINESCENCE; ENHANCEMENT; MICROSCOPY; EUROPIUM(III); DISTANCE; SENSORS; CELLS;
D O I
10.1038/s41598-019-47353-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Deep-ultraviolet excitation fluorescence microscopy has enabled molecular imaging having an optical sectioning capability with a wide-field configuration and its usefulness for slide-free pathology has been shown in recent years. Here, we report usefulness of terbium ions as RNA-specific labeling probes for slide-free pathology with deep-ultraviolet excitation fluorescence. On excitation in the wavelength range of 250-300 nm, terbium ions emitted fluorescence after entering cells. Bright fluorescence was observed at nucleoli and cytoplasm while fluorescence became weak after RNA decomposition by ribonuclease prior to staining. It was also found that the fluorescence intensity at nucleoplasm increased with temperature during staining and that this temperature-dependent behavior resembled temperature-dependent hypochromicity of DNA due to melting. These findings indicated that terbium ions stained single-stranded nucleic acid more efficiently than double-stranded nucleic acid. We further combined terbium ions and DNA-specific dyes for dual-color imaging. In the obtained image, nucleolus, nucleoplasm, and cytoplasm were distinguished. We demonstrated the usefulness of dual-color imaging for rapid diagnosis of surgical specimen by showing optical sectioning of unsliced tissues. The present findings can enhance deep-ultraviolet excitation fluorescence microscopy and consequently expand the potential of fluorescence microscopy in life sciences.
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页数:11
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