Structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications

被引:0
作者
Zhang, Tieqiao [1 ]
Osborn, Samantha [1 ,2 ]
Brandow, Chloe [1 ]
Dwyre, Denis [2 ]
Green, Ralph [2 ]
Lane, Stephen [1 ]
Wachsmann-Hogiu, Sebastian [1 ,2 ]
机构
[1] Univ Calif Davis, Ctr Biophoton Sci & Technol, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Pathol & Lab Med, Sch Med, Sacramento, CA 95817 USA
关键词
Super-resolution microscopy; structured illumination; blood cells; EOSIN-STAINED SECTIONS; FLUORESCENCE MICROSCOPY; RESOLUTION LIMIT; MEMBRANE; 3D;
D O I
10.1155/2013/261371
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Structured illumination fluorescence microscopy utilizes interfering light and the moire effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of resolution in the z- direction by the same factor of two (to approximately 220 nm), making it a powerful tool for 3-D morphology studies of fluorescently labeled cells or thin tissue sections. In this report, we applied this technique to several types of blood cells that are commonly seen in hematopathology. Compared with standard brightfield and ordinary fluorescence microscopy images, the 3-D morphology results clearly reveal the morphological features of different types of normal blood cells. We have also used this technique to evaluate morphologies of abnormal erythrocytes and compare them with those recorded on normal cells. The results give a very intuitive presentation of morphological structures of erythrocytes with great details. This research illustrates the potential of this technique to be used in hematology and cytopathology studies aimed at identifying nanometer-sized features that cannot be distinguished otherwise with conventional optical microscopy.
引用
收藏
页码:27 / 35
页数:9
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