TY - JOUR
T1 - Magnetically Promoted Rapid Immunofluorescence Staining for Frozen Tissue Sections
AU - Onishi, Tatsuya
AU - Matsuda, Sachiko
AU - Nakamura, Yuki
AU - Kuramoto, Junko
AU - Tsuruma, Akinori
AU - Sakamoto, Satoshi
AU - Suzuki, Shunichi
AU - Fuchimoto, Daiichiro
AU - Onishi, Akira
AU - Chikaki, Shinichi
AU - Kaneko, Miki
AU - Kuwahata, Akihiro
AU - Sekino, Masaki
AU - Yasuno, Hiroshi
AU - Hanyu, Naohiro
AU - Kurita, Tomoko
AU - Takei, Hiroyuki
AU - Sakatani, Takashi
AU - Taruno, Kanae
AU - Nakamura, Seigo
AU - Hayashida, Tetsu
AU - Jinno, Hiromitsu
AU - Kusakabe, Moriaki
AU - Handa, Hiroshi
AU - Kameyama, Kaori
AU - Kitagawa, Yuko
N1 - Funding Information:
Dr. Fumihiko Ishikawa (RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa) and the staff of Prime Tech Ltd. (Tsuchiura, Ibaraki, Japan) contributed to the development of RAG2 knockout swine. We thank Professor David Heery (The Nottingham University) for his support, the Collaborative Research Resources, School of Medicine, Keio University for technical assistance, and Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript. The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was supported by the Project for Medical Device Development from Japan Agency for Medical Research and Development, AMED under Grant Number JP18he0902010h0004.
Funding Information:
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was supported by the Project for Medical Device Development from Japan Agency for Medical Research and Development, AMED under Grant Number JP18he0902010h0004.
Publisher Copyright:
© The Author(s) 2019.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - 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).
AB - 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).
KW - cancer
KW - fluorescent ferrite beads
KW - immunostaining
KW - intraoperative diagnosis
KW - magnetic field
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U2 - 10.1369/0022155419841023
DO - 10.1369/0022155419841023
M3 - Article
C2 - 30958084
AN - SCOPUS:85064084120
SN - 0022-1554
VL - 67
SP - 575
EP - 587
JO - Journal of Histochemistry and Cytochemistry
JF - Journal of Histochemistry and Cytochemistry
IS - 8
ER -