Magnetically Promoted Rapid Immunofluorescence Staining for Frozen Tissue Sections

Author:

Onishi Tatsuya12,Matsuda Sachiko1,Nakamura Yuki1,Kuramoto Junko3,Tsuruma Akinori4,Sakamoto Satoshi4,Suzuki Shunichi5,Fuchimoto Daiichiro5,Onishi Akira6,Chikaki Shinichi7,Kaneko Miki7,Kuwahata Akihiro7,Sekino Masaki7,Yasuno Hiroshi8,Hanyu Naohiro8,Kurita Tomoko9,Takei Hiroyuki9,Sakatani Takashi10,Taruno Kanae11,Nakamura Seigo11,Hayashida Tetsu1,Jinno Hiromitsu12,Kusakabe Moriaki1314,Handa Hiroshi15,Kameyama Kaori16,Kitagawa Yuko1

Affiliation:

1. Department of Surgery, Keio University School of Medicine, Tokyo, Japan

2. Department of Breast Surgery, National Cancer Center Hospital East, Kashiwa, Japan

3. Department of Pathology, Keio University School of Medicine, Tokyo, Japan

4. School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan

5. Division of Animal Sciences, Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Japan

6. Laboratory of Animal Reproduction, Department of Animal Science and Resources, College of Bioresource Sciences, Nihon University, Fujisawa, Japan

7. Graduate School of Engineering, The University of Tokyo, Tokyo, Japan

8. Tamagawa Seiki Co. Ltd., Nagano, Japan

9. Department of Breast Surgery, Nippon Medical School, Tokyo, Japan

10. Department of Diagnostic Pathology, Nippon Medical School Hospital, Tokyo, Japan

11. Division of Breast Surgical Oncology, Showa University, Tokyo, Japan

12. Department of Surgery, Teikyo University School of Medicine, Tokyo, Japan

13. Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan

14. Matrix Cell Research Institute Inc., Ushiku, Japan

15. Department of Nanoparticle Translational Research, Tokyo Medical University, Tokyo, Japan

16. Department of Diagnostic Pathology, Keio University Hospital, Tokyo, Japan

Abstract

Current immunohistochemistry methods for diagnosing abnormal cells, such as cancer cells, require multiple steps and can be relatively slow compared with intraoperative frozen hematoxylin and eosin staining, and are therefore rarely used for intraoperative examination. Thus, there is a need for novel rapid detection methods. We previously demonstrated that functionalized fluorescent ferrite beads (FF beads) magnetically promoted rapid immunoreactions. The aim of this study was to improve the magnetically promoted rapid immunoreaction method using antibody-coated FF beads and a magnet subjected to a magnetic field. Using frozen sections of xenograft samples of A431 human epidermoid cancer cells that express high levels of epidermal growth factor receptor (EGFR) and anti-EGFR antibody-coated FF beads, we reduced the magnetically promoted immunohistochemistry procedure to a 1-min reaction and 1-min wash. We also determined the optimum magnetic force for the antibody reaction (from 7.79 × 10−15 N to 3.35 × 10−15 N) and washing (4.78 × 10−16 N), which are important steps in this technique. Furthermore, we stained paraffin-embedded tissue arrays and frozen sections of metastatic breast cancer lymph nodes with anti-pan-cytokeratin antibody-coated FF beads to validate the utility of this system in clinical specimens. Under optimal conditions, this ultra-rapid immunostaining method may provide an ancillary method for pathological diagnosis during surgery. (J Histochem Cytochem 58:XXX–XXX, 2010)

Publisher

SAGE Publications

Subject

Histology,Anatomy

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