フルテキストファイル
著者
Iyama, Takuji Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine / These authors contributed equally: Takuji Iyama and Tomoaki Takata.
Takata, Tomoaki Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine / These authors contributed equally: Takuji Iyama and Tomoaki Takata. 研究者総覧
Yamada, Kentaro Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Mae, Yukari Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Taniguchi, Sosuke Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Ida, Ayami Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Ogawa, Masaya Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Yamamoto, Marie Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Hamada, Shintaro Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Fukuda, Satoko Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine 研究者総覧
Kanda, Tsutomu Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine
Sugihara, Takaaki Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine 研究者総覧 KAKEN
Isomoto, Hajime Division of Gastroenterology and Nephrology, Tottori University Faculty of Medicine 研究者総覧 KAKEN
Urano, Yasuteru Laboratory of Chemical Biology and Molecular Imaging, Graduate School of Medicine, The University of Tokyo
抄録
Gamma-glutamyl hydroxymethyl rhodamine green (gGlu-HMRG) is an activatable fluorescent probe that can be activated by γ-glutamyltranspeptidase (GGT). The expression of GGT in the kidney, which is one of the major organs exhibiting enhanced GGT expression, is exclusively localised to the cortex. Here, we aimed to investigate the feasibility of gGlu-HMRG as a probe for the on-site assessment of renal biopsy specimens. gGlu-HMRG fluorescent probe was applied to the renal proximal tubular epithelial cells and cortical collecting duct cells in vitro, mouse kidneys ex vivo, and human biopsy specimens. In addition, the fluorescence intensities in the cortex and the medulla were comparatively evaluated in the biopsy specimens. The fluorescence signal was rapidly detected in the renal proximal tubular epithelial cells, whereas that in the cortical collecting duct cells was not detected. The fluorescence signal was detected in the mouse kidneys ex vivo without markedly affecting the tissue morphology. In the human biopsy specimens, the fluorescence signal in the cortex was significantly distinct from that in the medulla (p?<?0.05). Thus, this fluorescent probe can be used to distinctly identify the renal cortex in the biopsy specimens.
出版者
NATURE PUBLISHING GROUP
資料タイプ
学術雑誌論文
外部リンク
ISSN
20452322
掲載誌名
SCIENTIFIC REPORTS
10
発行日
2020-07
出版者DOI
著者版フラグ
出版社版
著作権表記
(C) The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
掲載情報
Iyama Takuji, Takata Tomoaki, Yamada Kentaro, et al. A novel method for assessing the renal biopsy specimens using an activatable fluorescent probe. SCIENTIFIC REPORTS. 2020. 10. doi:10.1038/s41598-020-69077-w
部局名
医学部・医学系研究科・医学部附属病院
言語
英語
Web of Science Key ut
WOS:000555519800009